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Merck
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文件

129682

Sigma-Aldrich

6-甲氧基-2-甲基苯并噻唑

97%

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About This Item

经验公式（希尔记法）:
C9H9NOS
CAS号:
2941-72-2
分子量:
179.24
Beilstein:
4457
EC號碼:
220-931-8
MDL號碼:
MFCD00005795
分類程式碼代碼:
12352100
PubChem物質ID:
24847921

品質等級

200

化驗

97%

形狀

liquid

折射率

n20/D 1.612 (lit.)

密度

1.204 g/mL at 25 °C (lit.)

SMILES 字串

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 密鑰

DYHLJSUORLPGNT-UHFFFAOYSA-N

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應用

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

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

228.2 °F - closed cup

閃點（°C）

109 °C - closed cup

個人防護裝備

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

分析证书(COA)

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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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