DE122569C - - Google Patents

Info

Publication number

DE122569C

DE122569C DENDAT122569D DE122569DA DE122569C DE 122569 C DE122569 C DE 122569C DE NDAT122569 D DENDAT122569 D DE NDAT122569D DE 122569D A DE122569D A DE 122569DA DE 122569 C DE122569 C DE 122569C

Authority

DE

Germany

Prior art keywords

amidophenol

rhodan

soluble

alcohol

acid

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.)

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• NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical group NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-N 0.000 claims description 9
• 238000000034 method Methods 0.000 claims description 3
• NYWVNRRGNPHTLI-UHFFFAOYSA-N 1,2-dichloro-3,4-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C(Cl)=C1[N+]([O-])=O NYWVNRRGNPHTLI-UHFFFAOYSA-N 0.000 claims description 2
• 238000006467 substitution reaction Methods 0.000 claims description 2
• CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
• 239000002253 acid Substances 0.000 description 5
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
• ZPXDNSYFDIHPOJ-UHFFFAOYSA-N 1,5-dichloro-2,4-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=C(Cl)C=C1Cl ZPXDNSYFDIHPOJ-UHFFFAOYSA-N 0.000 description 3
• 229960000583 Acetic Acid Drugs 0.000 description 3
• QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
• 230000001476 alcoholic Effects 0.000 description 3
• 239000012362 glacial acetic acid Substances 0.000 description 3
• 239000000203 mixture Substances 0.000 description 3
• 239000000243 solution Substances 0.000 description 3
• UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
• 125000001309 chloro group Chemical group Cl* 0.000 description 2
• 239000007859 condensation product Substances 0.000 description 2
• ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
• 239000011591 potassium Substances 0.000 description 2
• 229910052700 potassium Inorganic materials 0.000 description 2
• WCUXLLCKKVVCTQ-UHFFFAOYSA-M potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
• 239000000843 powder Substances 0.000 description 2
• 239000000047 product Substances 0.000 description 2
• VMHLLURERBWHNL-UHFFFAOYSA-M sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
• 239000001632 sodium acetate Substances 0.000 description 2
• 235000017281 sodium acetate Nutrition 0.000 description 2
• 159000000000 sodium salts Chemical class 0.000 description 2
• 210000003298 Dental Enamel Anatomy 0.000 description 1
• -1 Potassium chlorine Chemical compound 0.000 description 1
• XYFXKNMXCOSGOU-UHFFFAOYSA-N [N+](=O)([O-])OC=1C(=C(C=CC1)NC1=CC=CC=C1)O[N+](=O)[O-] Chemical class [N+](=O)([O-])OC=1C(=C(C=CC1)NC1=CC=CC=C1)O[N+](=O)[O-] XYFXKNMXCOSGOU-UHFFFAOYSA-N 0.000 description 1
• 239000007864 aqueous solution Substances 0.000 description 1
• 239000011230 binding agent Substances 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 238000001311 chemical methods and process Methods 0.000 description 1
• 239000007795 chemical reaction product Substances 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 238000009833 condensation Methods 0.000 description 1
• 230000005494 condensation Effects 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 238000000354 decomposition reaction Methods 0.000 description 1
• 239000003085 diluting agent Substances 0.000 description 1
• 239000000975 dye Substances 0.000 description 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
• OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
• 239000003960 organic solvent Substances 0.000 description 1
• 239000001103 potassium chloride Substances 0.000 description 1
• 235000011164 potassium chloride Nutrition 0.000 description 1
• 150000003839 salts Chemical class 0.000 description 1
• 239000011780 sodium chloride Substances 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 125000001424 substituent group Chemical group 0.000 description 1
• NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
• 239000011593 sulfur Substances 0.000 description 1
• 229910052717 sulfur Inorganic materials 0.000 description 1
• 238000010792 warming Methods 0.000 description 1

Cited By (1)