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Merck

663557

Sigma-Aldrich

2-氨基-5-(4-氟苯基)-1,3,4-噻重氮

97%

别名:

5-(4-氟苯基)-1,3,4-噻二唑-2-胺

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About This Item

经验公式(希尔记法):
C8H6FN3S
CAS号:
分子量:
195.22
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

97%

表单

solid

mp

238-243 °C

SMILES字符串

Nc1nnc(s1)-c2ccc(F)cc2

InChI

1S/C8H6FN3S/c9-6-3-1-5(2-4-6)7-11-12-8(10)13-7/h1-4H,(H2,10,12)

InChI key

WRSVCKNLHZWSNJ-UHFFFAOYSA-N

应用

2-Amino-5-(4-fluorophenyl)-1,3,4-thiadiazole can be used as a substrate in the preparation of:
  • Bithiophene based azo dyes with possible nonlinear optical (NLO) properties.
  • 4-Thiazolidinone derivatives as potent HCV NS5B polymerase inhibitors.
  • 1,3,4-Thiadiazole and phenothiazine hybrids as possible antitubercular agents.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

2-Heteroarylimino-5-arylidene-4-thiazolidinones as a new class of non-nucleoside inhibitors of HCV NS5B polymerase
Kucukguzel ?, et al.
European Journal of Medicinal Chemistry, 69(2), 931-941 (2013)
Design of new phenothiazine-thiadiazole hybrids via molecular hybridization approach for the development of potent antitubercular agents
Ramprasad J, et al.
European Journal of Medicinal Chemistry, 106(2), 75-84 (2015)
Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
Castro MR, et al.
Dyes and Pigments, 95(2), 392-399 (2012)

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