60093-15-4 Usage
Description
3-AMINO-5-PHENYLAMINO-1,2,4-THIADIAZOLE is a heterocyclic organic compound with the molecular formula C8H7N5S. It is a yellow crystalline solid that is used in the synthesis of pharmaceuticals and agrochemicals. 3-AMINO-5-PHENYLAMINO-1,2,4-THIADIAZOLE contains a thiadiazole ring with an amino group at the 3-position and a phenylamino group at the 5-position. It has a variety of potential applications in medicinal chemistry, including as a building block in the development of new therapeutic agents.
Uses
Used in Pharmaceutical Industry:
3-AMINO-5-PHENYLAMINO-1,2,4-THIADIAZOLE is used as a building block for the development of new therapeutic agents due to its potential applications in medicinal chemistry.
Used in Agrochemical Industry:
3-AMINO-5-PHENYLAMINO-1,2,4-THIADIAZOLE is used in the synthesis of agrochemicals, contributing to the development of new products for agricultural applications.
Used in Drug Discovery Research:
3-AMINO-5-PHENYLAMINO-1,2,4-THIADIAZOLE is used as a subject of interest in drug discovery research due to its demonstrated potential antitumor and antiviral activities.
Check Digit Verification of cas no
The CAS Registry Mumber 60093-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,9 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60093-15:
(7*6)+(6*0)+(5*0)+(4*9)+(3*3)+(2*1)+(1*5)=94
94 % 10 = 4
So 60093-15-4 is a valid CAS Registry Number.
60093-15-4Relevant articles and documents
Co-Catalyzed Intramolecular S-N Bond Formation in Water for 1,2-Benzisothiazol-3(2H)-ones and 1,2,4-Thiadiazoles Synthesis
Yang, Liting,Song, Lijuan,Tang, Shanyu,Li, Longjia,Li, Heng,Yuan, Bingxin,Yang, Guanyu
, p. 1281 - 1285 (2019/01/14)
An efficient and versatile Co-catalyzed intramolecular S-N bond formation in water to synthesize 1,2-benzisothiazol-3(2H)-one and 1,2,4-thiadiazoles derivatives in good to excellent yields was developed. The transformation showed great tolerance with a broad range of substituents. The mother liquor was able to be recycled 6 times with minor loss in product yield.
A facile synthesis of novel nitrogen-sulphur heterocycles containing the amidino moiety and their antimicrobial activity - Part I
Chande, Madhukar S.,Carvalho, Peter V. R.
, p. 378 - 384 (2007/10/03)
The interaction of amidinothiocarbamide 1 and 4-bromo-1,3-substituted-pyrazol-5-ones 1 afford 2-guanidino-4, 6-substituted-pyrazolo [5,4-d]thiazoles 5 on reaction with aldehydes yield the corresponding schiff's bases bases 6. An alternate unambiguous one