所有图片(1)
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
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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
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
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
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)
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)
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
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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