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Key Documents

Safety Information

129682

Sigma-Aldrich

6-Methoxy-2-methylbenzothiazole

97%

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About This Item

Empirical Formula (Hill Notation):
C9H9NOS
CAS Number:
Molecular Weight:
179.24
Beilstein:
4457
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
form:
liquid
Assay:
97%

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.612 (lit.)

density

1.204 g/mL at 25 °C (lit.)

SMILES string

COc1ccc2nc(C)sc2c1

InChI

1S/C9H9NOS/c1-6-10-8-4-3-7(11-2)5-9(8)12-6/h3-5H,1-2H3

InChI key

DYHLJSUORLPGNT-UHFFFAOYSA-N

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Application

6-Methoxy-2-methylbenzothiazole was used as an inhibitor of aryl hydrocarbon hydroxylase (PB/AHH) and aminopyrine N-demethylase (ADPM) in hepatic microsomes[1].

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

228.2 °F - closed cup

Flash Point(C)

109 °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

129682-1G:
129682-VAR:
129682-BULK:
129682-250MG:


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M Murray et al.
Chemico-biological interactions, 43(3), 341-351 (1983-03-01)
A series of benzimidazole derivatives containing additional fused and non-fused aromatic groupings were effective inhibitors of aryl hydrocarbon hydroxylase (PB/AHH) and aminopyrine N-demethylase (ADPM) activities in hepatic microsomes from phenobarbitone(PB)-induced rats. Two structurally similar nitrogen heterocycles, 6-ethoxy-2-methylbenzoxazole and 6-methoxy-2-methylbenzothiazole, were
[The public health service between yesterday and tomorrow (author's transl)].
L von Manger-Koenig
Das Offentliche Gesundheitswesen, 37(8), 433-448 (1975-08-01)

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