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101338

Benzothiazole

Name: Benzothiazole
Brand: ALDRICH

96%

Synonym(s):

1,3-Benzothiazole, Benzosulfonazole

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About This Item

Empirical Formula (Hill Notation):

C₇H₅NS

CAS Number:

95-16-9

Molecular Weight:

135.19

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24846538

EC Number:

202-396-2

Beilstein/REAXYS Number:

109468

MDL number:

MFCD00005775

Assay:

96%

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Properties

vapor density

4.66 (vs air)

Quality Level

100

vapor pressure

34 mmHg ( 131 °C)

assay

96%

refractive index

n20/D 1.642 (lit.)

bp

231 °C (lit.)

mp

2 °C (lit.)

density

1.238 g/mL at 25 °C (lit.)

SMILES string

c1ccc2scnc2c1

InChI

1S/C7H5NS/c1-2-4-7-6(3-1)8-5-9-7/h1-5H

InChI key

IOJUPLGTWVMSFF-UHFFFAOYSA-N

Description

Application

Interesting carbonyl equivalent. Reacts with aldehydes or ketones to generate α-hydroxy carbonyl compounds.

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pictograms

GHS06

signalword

Danger

hcodes

H301 + H311,H319,H332

pcodes

P261 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Irrit. 2

Storage Class

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

wgk

WGK 2

flash_point_f

224.6 °F - Pensky-Martens closed cup

flash_point_c

107 °C - Pensky-Martens closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Bulletin of the Chemical Society of Japan, 61, 3637-3637 (1988)

Synthesis and evaluation of antimicrobial activity of 4H-pyrimido[2,1-b]benzothiazole, pyrazole and benzylidene derivatives of curcumin.

Pramod K Sahu et al.

European journal of medicinal chemistry, 54, 366-378 (2012-06-12)

A novel, one-pot, simple, efficient procedure for 4H-pyrimido[2,1-b]benzothiazole (4a-h), pyrazole (6a-d) and benzylidene (7a-d) derivatives of curcumin under solvent and solvent free conditions in microwave with good yield is have been synthesized. The synthesized compounds were evaluated for their antibacterial

Optofluidic variable-focus lenses for light manipulation.

Y C Seow et al.

Lab on a chip, 12(19), 3810-3815 (2012-08-14)

This paper presents a planar optofluidic lens for light manipulation utilizing a combination of optofluidic biconvex lens with micromixer. Three light manipulation techniques including tunable optical diverging, collimating and focusing are realized by altering the refractive index of the optofluidic

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Global Trade Item Number

SKU	GTIN
101338-500G	04061838667793
101338-5G	04061838667809
101338-100G	04061838667779