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242659

Sigma-Aldrich

2-Bromothiophenol

97%

Synonym(s):

2-Bromobenzenethiol

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About This Item

Linear Formula:
BrC6H4SH
CAS Number:
6320-02-1
Molecular Weight:
189.07
Beilstein:
2039769
EC Number:
228-665-4
MDL number:
MFCD00004827
UNSPSC Code:
12352100
PubChem Substance ID:
24854576
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

refractive index

n20/D 1.635 (lit.)

bp

128-130 °C/25 mmHg (lit.)

density

1.573 g/mL at 25 °C (lit.)

SMILES string

Sc1ccccc1Br

InChI

1S/C6H5BrS/c7-5-3-1-2-4-6(5)8/h1-4,8H

InChI key

YUQUNWNSQDULTI-UHFFFAOYSA-N

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General description

2-Bromothiophenol (2-Bromobenzenethiol) reacts with 4-(4-bromo-3-nitro-phenyl)morpholine to form nitro-sulphide.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301,H315,H319,H335

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

>230.0 °F

Flash Point(C)

> 110 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Phenothiazynes: preparation of 2-and 3-tertiary aminophenothiazines.
Jones DH.
Journal of the Chemical Society, 132-137 (1971)
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
Homan Kang et al.
Scientific reports, 5, 10144-10144 (2015-05-29)
Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection, and biomolecular profiling processes. So far, several distinct encoding/decoding methods such as chemical encoding, graphical encoding, and optical encoding have been

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