IL26433A - Oregano complex compounds - tin that are the result of phosphoric acid and their preparation - Google Patents

Oregano complex compounds - tin that are the result of phosphoric acid and their preparation

Info

Publication number: IL26433A
Authority: IL; Israel
Prior art keywords: composition; group; formula; compounds; substituted
Prior art date: 1965-09-03

Application number

IL26433A

Other languages

English (en)

Hebrew (he)

Original Assignee

Boehringer Sohn Ingelheim

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1965-09-03

Filing date

1966-08-31

Publication date

1970-12-24

1966-08-31 Application filed by Boehringer Sohn Ingelheim filed Critical Boehringer Sohn Ingelheim

1970-12-24 Publication of IL26433A publication Critical patent/IL26433A/en

Links

238000002360 preparation method Methods 0.000 title claims description 7
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title description 4
229910000147 aluminium phosphate Inorganic materials 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims description 16
239000000203 mixture Substances 0.000 claims description 10
238000000034 method Methods 0.000 claims description 9
239000002253 acid Substances 0.000 claims description 8
125000005843 halogen group Chemical group 0.000 claims description 6
229910052799 carbon Inorganic materials 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
229910052698 phosphorus Inorganic materials 0.000 claims description 3
239000000126 substance Substances 0.000 claims description 3
239000004606 Fillers/Extenders Substances 0.000 claims description 2
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical group O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
239000005864 Sulphur Substances 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
125000000623 heterocyclic group Chemical group 0.000 claims description 2
229910052757 nitrogen Inorganic materials 0.000 claims description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 2
150000003016 phosphoric acids Chemical class 0.000 claims description 2
125000004437 phosphorous atom Chemical group 0.000 claims description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
229920002554 vinyl polymer Polymers 0.000 claims description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 1
229910021626 Tin(II) chloride Inorganic materials 0.000 claims 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
238000010410 dusting Methods 0.000 claims 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Chemical group SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
229910052760 oxygen Inorganic materials 0.000 claims 1
239000001301 oxygen Substances 0.000 claims 1
239000011574 phosphorus Substances 0.000 claims 1
239000000843 powder Substances 0.000 claims 1
239000003381 stabilizer Substances 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical group C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
230000003115 biocidal effect Effects 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
NJVOZLGKTAPUTQ-UHFFFAOYSA-M fentin chloride Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 NJVOZLGKTAPUTQ-UHFFFAOYSA-M 0.000 description 2
230000002363 herbicidal effect Effects 0.000 description 2
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
230000002265 prevention Effects 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
238000009736 wetting Methods 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
239000002023 wood Substances 0.000 description 2
241000228245 Aspergillus niger Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241000238008 Cerithidea rhizophorarum Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
208000035473 Communicable disease Diseases 0.000 description 1
241000283984 Rodentia Species 0.000 description 1
241000191967 Staphylococcus aureus Species 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
125000006323 alkenyl amino group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000005037 alkyl phenyl group Chemical group 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
125000005110 aryl thio group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
238000009472 formulation Methods 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000010985 leather Substances 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000002950 monocyclic group Chemical group 0.000 description 1
239000003973 paint Substances 0.000 description 1
-1 phenylhydrazino Chemical group 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
239000004753 textile Substances 0.000 description 1
125000004149 thio group Chemical group *S* 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/6533—Six-membered rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

IL26433A 1965-09-03 1966-08-31 Oregano complex compounds - tin that are the result of phosphoric acid and their preparation IL26433A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DEB83585A DE1298531B (de)	1965-09-03	1965-09-03	Verfahren zur Herstellung von Organozinnkomplexen

Publications (1)

Publication Number	Publication Date
IL26433A true IL26433A (en)	1970-12-24

Family

ID=6982043

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL26433A IL26433A (en)	1965-09-03	1966-08-31	Oregano complex compounds - tin that are the result of phosphoric acid and their preparation

Country Status (10)

Country	Link
US (1)	US3502690A (pt)
AT (1)	AT284542B (pt)
BE (1)	BE686314A (pt)
BR (1)	BR6682588D0 (pt)
CH (1)	CH490421A (pt)
DE (1)	DE1298531B (pt)
ES (2)	ES330802A1 (pt)
GB (1)	GB1160693A (pt)
IL (1)	IL26433A (pt)
NL (2)	NL6612312A (pt)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3947461A (en) *	1972-10-19	1976-03-30	Stauffer Chemical Company	Organotin miticidal and insecticidal compounds
US3947565A (en) *	1973-08-01	1976-03-30	Smithkline Corporation	Anti-arthritic compositions comprising s-heterocyclic derivatives of phosphine or phosphite gold mercaptides and methods of producing anti-arthritic activity
US3883546A (en) *	1973-08-01	1975-05-13	Smithkline Corp	S-heterocyclic derivatives of phosphine or phosphite gold mercaptides
US4018800A (en) *	1975-05-06	1977-04-19	Stauffer Chemical Company	Organotin miticidal and insecticidal compounds
US4554367A (en) *	1982-10-06	1985-11-19	Ciga-Geigy Corporation	Phosphonium organohalogenostannates-IV
KR102320939B1 (ko) *	2013-10-01	2021-11-03	가부시키가이샤 아데카	인 함유 화합물 및 그것을 함유하는 경화성 에폭시 수지 조성물

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1052529A (pt) *	1963-03-25

0
- NL NL131206D patent/NL131206C/xx active
1965
- 1965-09-03 DE DEB83585A patent/DE1298531B/de active Pending
1966
- 1966-08-25 CH CH1232466A patent/CH490421A/de not_active IP Right Cessation
- 1966-08-31 IL IL26433A patent/IL26433A/en unknown
- 1966-08-31 ES ES0330802A patent/ES330802A1/es not_active Expired
- 1966-08-31 NL NL6612312A patent/NL6612312A/xx unknown
- 1966-09-01 AT AT01444/67A patent/AT284542B/de not_active IP Right Cessation
- 1966-09-01 BE BE686314D patent/BE686314A/xx unknown
- 1966-09-02 GB GB39418/66A patent/GB1160693A/en not_active Expired
- 1966-09-02 BR BR182588/66A patent/BR6682588D0/pt unknown
- 1966-09-06 US US577197A patent/US3502690A/en not_active Expired - Lifetime
1967
- 1967-05-13 ES ES340546A patent/ES340546A1/es not_active Expired

Also Published As

Publication number	Publication date
US3502690A (en)	1970-03-24
BE686314A (pt)	1967-03-01
GB1160693A (en)	1969-08-06
DE1298531B (de)	1969-07-03
BR6682588D0 (pt)	1973-12-04
CH490421A (de)	1970-05-15
ES330802A1 (es)	1967-09-16
NL131206C (pt)
ES340546A1 (es)	1968-10-01
NL6612312A (pt)	1967-03-06
AT284542B (de)	1970-09-25

Publication	Publication Date	Title
US3523121A (en)	1970-08-04	Certain 2-carbamoyl-3-isothiazolenes
CA1139751A (en)	1983-01-18	3-isothiazolones as biocides
GB975046A (en)	1964-11-11	Halo-pyridyl phosphorus compounds
US3517022A (en)	1970-06-23	Certain 2-carbamoyl-1,2-benzisothiazolones
GB1019227A (en)	1966-02-02	Heterocyclic phosphate and thiophosphate derivatives
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US4041157A (en)	1977-08-09	Fungicidal pyrimidine derivatives
US3624091A (en)	1971-11-30	Oxime-o-carbonic acid esters
IL26433A (en)	1970-12-24	Oregano complex compounds - tin that are the result of phosphoric acid and their preparation
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US3544580A (en)	1970-12-01	Certain acyl derivatives of oxo- and oxyisothiazoles
US4062859A (en)	1977-12-13	Halogenated 3-isothiazolidinone 1-oxide and 1,1-dioxides
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US3653873A (en)	1972-04-04	Ethylenic sulfilimine compositions for controlling fungi, bacteria and algae
KR870007896A (ko)	1987-09-22	2-시아노벤즈이미다졸 유도체의 제조방법
EP0049643B1 (en)	1985-07-17	Improvements in or relating to bis(substituted phenyl) alkyltin compounds
EP0123931B1 (en)	1988-12-21	Furan derivatives having fungicide activity
US3542865A (en)	1970-11-24	Ethylenic sulfilimines
US3790677A (en)	1974-02-05	Control of phytopathogenic fungi with 3-arylimino-1,2-dithiols
US3706757A (en)	1972-12-19	Certain organotin derivatives of 3-hydroxyisothiazole
US3523951A (en)	1970-08-11	1,3,4-thiadiazole-5(4h)-one derivatives
EP0412681B1 (en)	1994-09-28	Azolidine derivatives, process for preparing the same and agricultural and horticultural fungicide