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
Bulletin of the Chemical Society of Japan, 61, 3637-3637 (1988)
Pramod K Sahu et al.
European journal of medicinal chemistry, 54, 366-378 (2012-06-12)
A novel, one-pot, simple, efficient procedure for 4H-pyrimido[2,1-b]benzothiazole (4a-h), pyrazole (6a-d) and benzylidene (7a-d) derivatives of curcumin under solvent and solvent free conditions in microwave with good yield is have been synthesized. The synthesized compounds were evaluated for their antibacterial
Y C Seow et al.
Lab on a chip, 12(19), 3810-3815 (2012-08-14)
This paper presents a planar optofluidic lens for light manipulation utilizing a combination of optofluidic biconvex lens with micromixer. Three light manipulation techniques including tunable optical diverging, collimating and focusing are realized by altering the refractive index of the optofluidic
Liang-Hua Zou et al.
Chemical communications (Cambridge, England), 48(92), 11307-11309 (2012-10-18)
A convenient transition metal-free procedure for the direct thiolation of 1,3,4-oxadiazole C-H bonds using diaryl disulfides has been developed. Other substrates including indole, benzothiazole, N-phenylbenzimidazole, and caffeine were also thiolated in this manner, providing the corresponding products in good to
Gabriel Navarrete-Vazquez et al.
European journal of medicinal chemistry, 53, 346-355 (2012-05-16)
The ethyl 2-(6-substituted benzo[d]thiazol-2-ylamino)-2-oxoacetate derivatives (OX 1-9) were prepared using a one-step reaction. The in vitro inhibitory activity of the compounds against protein tyrosine phosphatase 1B (PTP-1B) was evaluated. Compounds OX-(1, 6 and 7) were rapid reversible (mixed-type) inhibitors of
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