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101338

苯并噻唑

96%

别名:

1,3-Benzothiazole, Benzosulfonazole

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关于此项目

经验公式（希尔记法）:
C7H5NS
化学文摘社编号:
95-16-9
分子量:
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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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

Application

备受关注的羰基等价物。与醛类或酮类反应可生成 α-羟基羰基化合物。

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pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

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

存储类别

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SDBB8332
SDBB0482
STBL1565
STBK8203
STBK1793

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Journal of medicinal chemistry, 56(9), 3531-3545 (2013-04-23)
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European journal of medicinal chemistry, 58, 206-213 (2012-11-06)
A series of N-(substituted benzothiazol-2-yl)amide derivatives 2a-h and 4a-h were synthesized by the EDC coupling reactions of substituted-benzothiazol-2-amine with 4-oxo-4-phenylbutanoic acid/2-benzoyl benzoic acid and evaluated for their anticonvulsant and neuroprotective effect. N-(6-methoxybenzothiazol-2-yl)-4-oxo-4-phenylbutanamide (2f) emerged as the most effective anticonvulsant with
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全球贸易项目编号

货号GTIN
101338-500G04061838667793
101338-5G04061838667809
101338-100G04061838667779