GB2003495A - Improvements in or relating to organic compounds - Google Patents
Improvements in or relating to organic compoundsInfo
- Publication number
- GB2003495A GB2003495A GB7835142A GB7835142A GB2003495A GB 2003495 A GB2003495 A GB 2003495A GB 7835142 A GB7835142 A GB 7835142A GB 7835142 A GB7835142 A GB 7835142A GB 2003495 A GB2003495 A GB 2003495A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrogen
- alkyl
- image
- radical
- substituted
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- 150000002894 organic compounds Chemical class 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 239000001257 hydrogen Substances 0.000 abstract 9
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 150000002431 hydrogen Chemical group 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 230000008878 coupling Effects 0.000 abstract 3
- 238000010168 coupling process Methods 0.000 abstract 3
- 238000005859 coupling reaction Methods 0.000 abstract 3
- 125000004958 1,4-naphthylene group Chemical group 0.000 abstract 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 1
- 239000000986 disperse dye Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/095—Amino naphthalenes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/0003—Monoazo dyes prepared by diazotising and coupling from diazotized anilines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
- C09B29/0805—Amino benzenes free of acid groups
- C09B29/0807—Amino benzenes free of acid groups characterised by the amino group
- C09B29/0809—Amino benzenes free of acid groups characterised by the amino group substituted amino group
- C09B29/0811—Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino
- C09B29/0813—Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino substituted by OH, O-C(=X)-R, O-C(=X)-X-R, O-R (X being O,S,NR; R being hydrocarbonyl)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paints Or Removers (AREA)
Abstract
The present invention relates to disperse dyes of formula I <IMAGE> in which D is a diazo component radical K is the radical of a coupling component of the 1,4-phenylene or 1,4- naphthylene series, R1 is hydrogen; alkyl; or alkenyl; and when K is a coupling component radical of the 1,4- phenylene series, R1 is also alkenyl mono-substituted by halogen; or alkyl mono-substituted, R2 is hydrogen, acyl, alkyl or alkyl mono-substituted, <IMAGE> with the proviso that when R4 is <IMAGE> K is a coupling component radical of the 1,4-naphthylene series, R5 is hydrogen, or <IMAGE> each of R3 and R'3 is hydrogen or alkyl, together with the adjacent carbon atoms form a cyclohexane ring with the proviso that when R3 and R'3 are cyclohexane R5 is hydrogen, one of R6 and R'6 is hydrogen and the other is hydrogen or halogen, R7, R8 and R'8 is hydrogen or alkyl, R9 is hydrogen, acyl, alkyl or alkyl monosubstituted.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1080077A CH630105A5 (en) | 1977-09-05 | 1977-09-05 | Process for preparing organic compounds |
CH1424177 | 1977-11-22 | ||
CH402578A CH631199A5 (en) | 1978-04-14 | 1978-04-14 | Azo compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2003495A true GB2003495A (en) | 1979-03-14 |
GB2003495B GB2003495B (en) | 1982-03-03 |
Family
ID=27174672
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7835142A Expired GB2003495B (en) | 1977-09-05 | 1978-08-31 | Organic compounds |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPS5450029A (en) |
BR (1) | BR7805743A (en) |
DD (1) | DD139720A5 (en) |
DE (1) | DE2837121A1 (en) |
ES (1) | ES473060A1 (en) |
FR (1) | FR2401959B1 (en) |
GB (1) | GB2003495B (en) |
IT (1) | IT7850937A0 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3015121A1 (en) * | 1979-05-03 | 1980-11-13 | Sandoz Ag | 4-HALOGEN-5-FORMYLTHIAZOLE COMPOUNDS |
US4609727A (en) * | 1981-12-21 | 1986-09-02 | Sandoz Ltd. | 5-C1-4 alkoxy-2-C1-2 alkyl-2',4'-dinitro-6'-halo-4-substituted amino-azobenzenes |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3715424A1 (en) * | 2019-03-27 | 2020-09-30 | DyStar Colours Distribution GmbH | High wet fast disperse dye mixtures of n-[4-(5-thiocyanato-2,4-dinitro-phenylazo)-phenyl]-amine derivatives and n-[4-(4-nitro-phenylazo)-phenyl]-amine derivatives |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3562789A (en) * | 1966-08-12 | 1971-02-09 | Mitsui Toatsu Chemicals | Monoazodyestuffs containing a 3-n-(beta-hydroxy- alpha - cyclohexyloxy or aryloxy) propylamino-4-alkoxy-alranoylanilide group |
FR1534269A (en) * | 1966-08-12 | 1968-07-26 | Mitsui Kagaku Kogyo Kabushiki | New monoazo dyes |
CH497503A (en) * | 1968-11-07 | 1970-10-15 | Geigy Ag J R | Process for the production of azo dyes which are sparingly soluble in water |
JPS5013681A (en) * | 1973-06-11 | 1975-02-13 |
-
1978
- 1978-08-25 DE DE19782837121 patent/DE2837121A1/en not_active Withdrawn
- 1978-08-31 FR FR7825161A patent/FR2401959B1/en not_active Expired
- 1978-08-31 GB GB7835142A patent/GB2003495B/en not_active Expired
- 1978-09-01 IT IT7850937A patent/IT7850937A0/en unknown
- 1978-09-04 BR BR7805743A patent/BR7805743A/en unknown
- 1978-09-04 DD DD78207637A patent/DD139720A5/en unknown
- 1978-09-04 JP JP10768978A patent/JPS5450029A/en active Granted
- 1978-09-04 ES ES473060A patent/ES473060A1/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3015121A1 (en) * | 1979-05-03 | 1980-11-13 | Sandoz Ag | 4-HALOGEN-5-FORMYLTHIAZOLE COMPOUNDS |
US4609727A (en) * | 1981-12-21 | 1986-09-02 | Sandoz Ltd. | 5-C1-4 alkoxy-2-C1-2 alkyl-2',4'-dinitro-6'-halo-4-substituted amino-azobenzenes |
Also Published As
Publication number | Publication date |
---|---|
GB2003495B (en) | 1982-03-03 |
JPS6216981B2 (en) | 1987-04-15 |
FR2401959B1 (en) | 1985-11-22 |
ES473060A1 (en) | 1979-10-16 |
BR7805743A (en) | 1979-05-15 |
FR2401959A1 (en) | 1979-03-30 |
DE2837121A1 (en) | 1979-03-15 |
DD139720A5 (en) | 1980-01-16 |
IT7850937A0 (en) | 1978-09-01 |
JPS5450029A (en) | 1979-04-19 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |