20166-91-0 Usage
Description
(2-amino-1,3-thiazol-4-yl)methyl carbamimidothioate dihydrochloride is a chemical compound that features a thiazole ring with an amino group and a carbamimidothioate group. The dihydrochloride form of the molecule is a salt, with two chloride anions associated with it. Thiazole derivatives are recognized for their diverse biological activities, such as antimicrobial, antitumor, and anti-inflammatory properties, which makes this compound a promising candidate for pharmaceuticals and organic synthesis. The carbamimidothioate group also suggests specific reactivity and utility in chemical reactions, particularly in medicinal chemistry and drug development.
Uses
Used in Pharmaceutical Industry:
(2-amino-1,3-thiazol-4-yl)methyl carbamimidothioate dihydrochloride is used as a pharmaceutical intermediate for its potential to contribute to the development of drugs with antimicrobial, antitumor, and anti-inflammatory effects. The presence of the thiazole ring and the carbamimidothioate group provides a structural foundation for the compound to be further modified and optimized for specific therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (2-amino-1,3-thiazol-4-yl)methyl carbamimidothioate dihydrochloride serves as a versatile building block. Its unique structure allows it to be a key component in the synthesis of more complex organic molecules, potentially leading to the creation of new compounds with specialized properties for various applications, including but not limited to the development of new pharmaceuticals, agrochemicals, or materials science advancements.
Used in Medicinal Chemistry:
(2-amino-1,3-thiazol-4-yl)methyl carbamimidothioate dihydrochloride is utilized in medicinal chemistry for its potential to be a part of drug discovery processes. (2-amino-1,3-thiazol-4-yl)methyl carbamimidothioate dihydrochloride's reactivity and structural features make it suitable for the design and synthesis of new molecules with therapeutic potential. Researchers can exploit its chemical properties to create novel drug candidates that target specific biological pathways or receptors.
Check Digit Verification of cas no
The CAS Registry Mumber 20166-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,6 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20166-91:
(7*2)+(6*0)+(5*1)+(4*6)+(3*6)+(2*9)+(1*1)=80
80 % 10 = 0
So 20166-91-0 is a valid CAS Registry Number.