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129682

Sigma-Aldrich

6-Methoxy-2-methylbenzothiazole

97%

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About This Item

Empirical Formula (Hill Notation):
C9H9NOS
CAS Number:
2941-72-2
Molecular Weight:
179.24
Beilstein:
4457
EC Number:
220-931-8
MDL number:
MFCD00005795
UNSPSC Code:
12352100
PubChem Substance ID:
24847921
form:
liquid
Assay:
97%
Pricing and availability is not currently available.

Quality Level

200

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW2251
BCBR1668V
BCBQ3550V
BCBK0076V
1437845V

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[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)
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

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