- CAS 17467-15-1
- Purity 99%
Location：Home > Others > 5-AMINO-3-PHENYL-1,2,4-THIADIAZOLE
Buy Good Quality 5-AMINO-3-PHENYL-1,2,4-THIADIAZOLE 17467-15-1 with a minimum purity of 99%
- Molecular Formula: C8H7N3S
- Molecular Weight: 177.23
- Appearance/Colour: light brownish fine crystalline powder
- Vapor Pressure: 2.45E-05mmHg at 25°C
- Melting Point: 152-156 °C
- Refractive Index: 1.669
- Boiling Point: 359 °C at 760 mmHg
- Flash Point: 170.9 °C
- PSA： 80.04000
- Density: 1.333 g/cm3
- LogP: 2.36850
5-AMINO-3-PHENYL-1,2,4-THIADIAZOLE(Cas 17467-15-1) Usage
InChI:InChI=1/C8H7N3S/c9-8-10-7(11-12-8)6-4-2-1-3-5-6/h1-5H,(H2,9,10,11)
17467-15-1 Relevant articles
One-Pot Synthesis of 3-Aryl-5-amino-1,2,4-thiadiazoles from Imidates and Thioureas by I2-Mediated Oxidative Construction of the N–S Bond
Chai, Ling,Lai, Zhenzhen,Xia, Qiangqiang,Yuan, Jiangpei,Bian, Qilong,Yu, Mingjian,Zhang, Wenkai,Xu, Yuanqing,Xu, Hao
, p. 4338 - 4344 (2018/08/31)
A simple and practical method for the on...
Copper-Catalyzed Aerobic Oxidative [3+2] Annulation for the Synthesis of 5-Amino/Imino-Substituted 1,2,4-Thiadiazoles through C-N/N-S Bond Formation
Yu, Wentao,Huang, Yubing,Li, Jianxiao,Tang, Xiaodong,Wu, Wanqing,Jiang, Huanfeng
, p. 9334 - 9343 (2018/07/30)
A copper-catalyzed aerobic oxidative ann...
Facile synthesis of substituted 5-amino- And 3-amino-1,2,4-thiadiazoles from a common precursor
Wehn, Paul M.,Harrington, Paul E.,Eksterowicz, John E.
scheme or table, p. 5666 - 5669 (2010/03/01)
[Chemical Equation Presented] A novel ap...
Pyrimidine benzamide-based thrombopoietin receptor agonists
Reiter, Lawrence A.,Subramanyam, Chakrapani,Mangual, Emilio J.,Jones, Christopher S.,Smeets, Marc I.,Brissette, William H.,McCurdy, Sandra P.,Lira, Paul D.,Linde, Robert G.,Li, Qifang,Zhang, Fangning,Antipas, Amy S.,Blumberg, Laura C.,Doty, Jonathan L.,Driscoll, James P.,Munchhof, Michael J.,Ripp, Sharon L.,Shavnya, Andrei,Shepard, Richard M.,Sperger, Diana,Thomasco, Lisa M.,Trevena, Kristen A.,Wolf-Gouveia, Lilli A.,Zhang, Liling
, p. 5447 - 5454 (2008/03/11)
A series of pyrimidine benzamide-based t...
17467-15-1 Process route
-
-
N-carbamothioylbenzimidamide
-
-
17467-15-1
2-amino-4-phenyl-1,3,5-thiadiazole
Conditions
| Conditions | Yield |
|---|---|
|
With
iodine;
In
water; dimethyl sulfoxide;
at 25 ℃;
for 10h;
Reagent/catalyst;
Sealed tube;
Schlenk technique;
|
88%
|
-
-
1101173-93-6
3-bromo-5-amino-1,2,4-thiadiazole
-
-
98-80-6
phenylboronic acid
-
-
17467-15-1
2-amino-4-phenyl-1,3,5-thiadiazole
Conditions
| Conditions | Yield |
|---|---|
|
With
bis(tri-tert-butylphosphine)palladium(0); caesium carbonate;
In
1,4-dioxane; water;
at 80 ℃;
|
13%
|
17467-15-1 Upstream products
-
71017-37-3
N -bromo-benzamidine
-
333-20-0
potassium thioacyanate
-
1670-14-0
benzamidine monohydrochloride
-
888-71-1
3,5-diphenyl-1,2,4-oxadiazole
17467-15-1 Downstream products
-
93021-01-3
4-acetylamino-N -(3-phenyl-[1,2,4]thiadiazol-5-yl)-benzenesulfonamide
-
69225-18-9
4-methyl-3-phenyl-4H -[1,2,4]thiadiazol-5-ylideneamine
-
73171-46-7
N-Nitroso-3-phenyl-1,2,4-thiadiazol-5-amin
-
16132-83-5
1-phenyl-5a,6,7,8,9,9a-hexahydro-6,9-methano-benzo[e ][1,2,4]thiadiazolo[5,4-c ][1,2,4]thiadiazine 5-oxide