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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%
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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
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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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