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441910

6-Bromo-2-benzothiazolinone

Name: 6-Bromo-2-benzothiazolinone
Brand: ALDRICH

98%

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About This Item

Empirical Formula (Hill Notation):

C₇H₄BrNOS

CAS Number:

62266-82-4

Molecular Weight:

230.08

MDL number:

MFCD00239363

UNSPSC Code:

12352100

PubChem Substance ID:

24867712

NACRES:

NA.22

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Assay

98%

mp

229-233 °C (lit.)

SMILES string

Brc1ccc2NC(=O)Sc2c1

InChI

1S/C7H4BrNOS/c8-4-1-2-5-6(3-4)11-7(10)9-5/h1-3H,(H,9,10)

InChI key

HECJMTPEVWQFCY-UHFFFAOYSA-N

General description

Synthesis of 6-bromo-2-benzothiazolinone has been reported.[1] Density of 6-bromo-2-benzothiazolinone is 1.7496 g/cm³ at 25°C.[2]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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3-Substituted 6-Bromo-2-benzothiazolinones and Their Antialgal and Plant Growth Regulating Activity.

Sidoova E, et al.

Chemical Papers, 46(2), 112-115 (1992)

Yaws CL.

The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 2, 136-136 (2015)

Effects of 2-alkylthio-6-aminobenzothiazoles and their 6-N-substituted derivatives on photosynthesis inhibition in Chlorella vulgaris and spinach chloroplasts.

K Král'ová et al.

General physiology and biophysics, 12(5), 421-427 (1993-10-01)

2-Alkylthio-6-aminobenzothiazoles and their 6-N-substituted derivatives 3-(2-alkylthio-6-benzothiazolylaminomethyl)-2-benzothiazolineth iones and 3-(2-alkylthio-6-benzothiazolylaminomethyl)-6-bromo-2-benzothia zolinones inhibit photosynthetic processes in spinach chloroplasts and the chlorophyll production in Chlorella vulgaris. The inhibitory activity depends on the alkyl chain length of the thioalkyl substituent. The site of action

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