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Merck
CN

196924

Sigma-Aldrich

2-氨基-5-乙基-1,3,4-噻二唑

97%

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About This Item

经验公式(希尔记法):
C4H7N3S
CAS号:
分子量:
129.18
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

检测方案

97%

mp

200-203 °C (lit.)

SMILES字符串

CCc1nnc(N)s1

InChI

1S/C4H7N3S/c1-2-3-6-7-4(5)8-3/h2H2,1H3,(H2,5,7)

InChI key

QXTRPGAMVIONMK-UHFFFAOYSA-N

一般描述

Influence of 2-amino-5-ethylthio-1,3,4-thiadiazole on inhibition of copper corrosion in an aerated 0.50M HCl solution has been investigated using gravimetric and electrochemical techniques.

应用

2-Amino-5-ethyl-1,3,4-thiadiazole was used in the synthesis of:
  • 3-(5-ethyl-1,3,4-thiadiazol-2-yldiazenyl)-1-methyl-2-phenyl-1H-indole
  • hetarylazoindole dyes
  • N-(5-ethyl-[1,3,4]-thiadiazole-2-yl) toluenesulfonamide ligand

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

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


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3-(5-Ethyl-1, 3, 4-thiadiazol-2-yldiazenyl)-1-methyl-2-phenyl-1H-indole.
Seferoglu Z, et al.
Acta Crystallographica Section E, Structure Reports Online, 63(2), o568-o570 (2007)
Effects of 2-amino-5-ethylthio-1, 3, 4-thiadiazole on copper corrosion as a corrosion inhibitor in aerated acidic pickling solutions.
Sherif EM and Park S-M.
Electrochimica Acta, 51(28), 6556-6562 (2006)
Adriana Hangan et al.
Acta crystallographica. Section B, Structural science, 66(Pt 6), 615-621 (2010-11-26)
The crystal structure solution of the title compound is determined from microcrystalline powder using a multi-technique approach that combines X-ray powder diffraction (XRPD) data analysis based on direct-space methods with information from (13)C solid-state NMR (SSNMR), and molecular modelling using
The synthesis, spectroscopic properties and crystal structure of novel, bis-hetarylazo disperse dyes.
Seferoglu Z, et al.
Dyes and Pigments, 77(3), 614-625 (3008)
Damien Cressier et al.
Bioorganic & medicinal chemistry, 17(14), 5275-5284 (2009-06-09)
In this work, we report the synthesis and characterization of new compounds derived from benzothiazoles and thiadiazoles. We observed that structural modifications on these skeletons affected the antioxidant activity. Thiol and aminothiol compounds derived from thiadiazoles and benzothiazoles showed an

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