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2-Amino-4-chlorothiophenol

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2-Amino-4-chlorothiophenol Basic information
Product Name:2-Amino-4-chlorothiophenol
Synonyms:BUTTPARK 35\10-17;4-Chloro-2-Aminothio-Phenol;2-amino-4-chloro thoiphenol;4-Chloro-2-aminobenzenethiol;5-Chloro-2-mercaptoaniline, 2-Amino-4-chlorobenzenethiol, 2-Amino-4-chlorophenyl mercaptan;2-Amino-4-chlorobenzenethiol 96%;2-AMINO-4-CHLORO THIOPHENOL 97.0%MIN;5-Chloro-2-mercaptoaniline
CAS:1004-00-8
MF:C6H6ClNS
MW:159.64
EINECS:
Product Categories:Sulphur Derivatives;Phenol&Thiophenol&Mercaptan;Phenoles and thiophenoles;Organic Building Blocks;Sulfur Compounds;Thiols/Mercaptans
Mol File:1004-00-8.mol
2-Amino-4-chlorothiophenol Structure
2-Amino-4-chlorothiophenol Chemical Properties
Melting point 56-61 °C (lit.)
Boiling point 100 °C(Press: 1 Torr)
density 1.372±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
Water Solubility Practically insoluble in water
solubility Chloroform (Slightly), Methanol (Sparingly)
pka7.35±0.11(Predicted)
form powder to crystaline
color White to Light yellow to Green
Sensitive Stench
Stability:Air sensitive, Light sensitive
InChI1S/C6H6ClNS/c7-4-1-2-6(9)5(8)3-4/h1-3,9H,8H2
InChIKeyNGIRMPARLVGMPX-UHFFFAOYSA-N
SMILESNc1cc(Cl)ccc1S
CAS DataBase Reference1004-00-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
RIDADR UN 3261 8/PG 3
WGK Germany 3
Hazard Note Irritant/Stench
HazardClass 8
PackingGroup III
HS Code 29309090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2-Amino-4-chlorothiophenol Usage And Synthesis
Chemical PropertiesYellow crystalline
Uses2-Amino-4-chlorobenzenethiol may be used in the synthesis of:
  • 2,3-dihydro-1,5-benzothiazepin-4-(5H)-ones
  • 8-chloro-1-azaphenothiazine
  • 5-chloro-2-(4-methoxyphenyl)-2,3-dihydro-1,3,2-benzothiazaphosphole 2-sulfide
General Description2-Amino-4-chlorobenzenethiol reacts with aromatic aldehydes and cyclohexanecarboxaldehyde to afford the corresponding thiazole and thiazoline derivatives. It undergoes oxidation in the presence of 1-n-butyl-3-methylimidazolium methylselenite, [bmim][SeO2(OCH3)] to form the corresponding symmetrical disulfide.
Tag:2-Amino-4-chlorothiophenol(1004-00-8) Related Product Information
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