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242675

Sigma-Aldrich

3-Chlorobenzenethiol

97%

Synonym(s):

3-Chlorothiophenol

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About This Item

Linear Formula:
ClC6H4SH
CAS Number:
2037-31-2
Molecular Weight:
144.62
EC Number:
218-010-0
MDL number:
MFCD00004839
UNSPSC Code:
12352100
PubChem Substance ID:
24854577

Assay

97%

form

liquid

refractive index

n20/D 1.6021 (lit.)

bp

110 °C/30 mmHg (lit.)

density

1.245 g/mL at 25 °C (lit.)

SMILES string

Sc1cccc(Cl)c1

InChI

1S/C6H5ClS/c7-5-2-1-3-6(8)4-5/h1-4,8H

InChI key

CQJDYPZUDYXHLM-UHFFFAOYSA-N

General description

The transfer constant of 3-chlorobenzenethiol (3-chlorothiophenol) in the polymerization of methyl methacrylate was studied.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

194.0 °F - closed cup

Flash Point(C)

90 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

242675-VAR:
242675-1G:
242675-BULK:
242675-10G:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The effect of phenols and aromatic thiols on the polymerization of methyl methacrylate.
Canadian Journal of Chemistry, 41(11), 2737-2742 (1963)
Javier Campanini-Salinas et al.
Molecules (Basel, Switzerland), 23(7) (2018-07-22)
A rapid emergence of resistant bacteria is occurring worldwide, endangering the efficacy of antibiotics and reducing the therapeutic arsenal available for treatment of infectious diseases. In the present study, we developed a new class of compounds with antibacterial activity obtained

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