19723-92-3 Usage
Description
Ethanone, 2-[[4-amino-5-(4-bromobenzoyl)-2-thiazolyl]thio]-1-(4-bromophenyl)-, is a complex thioamide compound characterized by the presence of a thiazole ring with an amino group and a bromobenzoyl group. It also features a thioether linkage and a 4-bromophenyl group, both of which are substituted with bromine atoms. This unique structure may endow it with potential applications in various fields, such as pharmaceuticals and agrochemicals, although further research is required to explore its specific uses and properties.
Uses
Used in Pharmaceutical Industry:
Ethanone, 2-[[4-amino-5-(4-bromobenzoyl)-2-thiazolyl]thio]-1-(4-bromophenyl)-, is used as a potential pharmaceutical compound for its unique chemical structure and properties. Its thioamide and bromophenyl groups may contribute to its interaction with biological targets, making it a candidate for the development of new drugs with specific therapeutic effects.
Used in Agrochemical Industry:
Ethanone, 2-[[4-amino-5-(4-bromobenzoyl)-2-thiazolyl]thio]-1-(4-bromophenyl)-, may also find applications in the agrochemical industry, where its unique structure could be utilized for the development of novel pesticides or herbicides. Further research is needed to explore its potential as an active ingredient in these products and to assess its efficacy and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 19723-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,2 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19723-92:
(7*1)+(6*9)+(5*7)+(4*2)+(3*3)+(2*9)+(1*2)=133
133 % 10 = 3
So 19723-92-3 is a valid CAS Registry Number.
19723-92-3Relevant articles and documents
A New Synthesis of Substituted 4-Amino-1,3-thiazoles
Evers, R.
, p. 604 - 608 (2007/10/02)
In the 5-position substituted 4-amino-2-alkylthio-1,3-thiazoles are prepared in good yields from N-nitro-amidino-dithiocarbamates 1 and α-halogen-carbonylcompounds or chloracetonitrile. 1 reacts with 1,3-dichlor-acetone under formation of adequate bis(1,3
