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%
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。
signalword
Danger
hcodes
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
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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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The synthesis and SAR of new β-amyloid binding agents are reported. Evaluation of important properties for achieving good signal-to-background ratio is described. Compounds 27, 33, and 36 displayed desirable lipophilic and pharmacokinetic properties. Compound 27 was further evaluated with autoradiographic
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