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Merck
CN

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:
分子量:
135.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-396-2
Beilstein/REAXYS Number:
109468
MDL number:
Assay:
96%
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InChI key

IOJUPLGTWVMSFF-UHFFFAOYSA-N

InChI

1S/C7H5NS/c1-2-4-7-6(3-1)8-5-9-7/h1-5H

SMILES string

c1ccc2scnc2c1

vapor density

4.66 (vs air)

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.)

Quality Level

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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。

pictograms

Skull and crossbones

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

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Bulletin of the Chemical Society of Japan, 61, 3637-3637 (1988)
Mohd Zaheen Hassan et al.
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
Ruiqing Ni et al.
Brain : a journal of neurology, 136(Pt 7), 2217-2227 (2013-06-13)
Imaging fibrillar amyloid-β deposition in the human brain in vivo by positron emission tomography has improved our understanding of the time course of amyloid-β pathology in Alzheimer's disease. The most widely used amyloid-β imaging tracer so far is (11)C-Pittsburgh compound
Seunghee Hong et al.
Journal of medicinal chemistry, 56(9), 3531-3545 (2013-04-23)
The existence of drug resistance caused by mutations in the break-point cluster region-Abelson tyrosine kinase (Bcr-Abl) kinase domain remains a clinical challenge due to limited effective treatment options for chronic myeloid leukemia (CML). Herein we report a novel series of
Ahmed Kamal et al.
Bioorganic & medicinal chemistry, 20(11), 3480-3492 (2012-05-01)
A series of chalcone-amidobenzothiazole conjugates (9a-k and 10a,b) have been synthesized and evaluated for their anticancer activity. All these compounds exhibited potent activity and the IC(50) of two potential compounds (9a and 9f) against different cancer cell lines are in

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