13306-99-5 Usage
Uses
Used in Organic Synthesis:
2-PHENYL-2H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure and functional groups allow for a wide range of chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-PHENYL-2H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID is utilized as a key building block for the development of pharmaceuticals. Its structure and properties enable the creation of new compounds with potential therapeutic effects, contributing to the discovery of novel drugs for various diseases.
Used in Agrochemicals:
2-PHENYL-2H-1,2,3-TRIAZOLE-4-CARBOXYLIC ACID also finds application in the agrochemical industry, where it is employed as a starting material for the synthesis of agrochemicals with pesticidal properties. Its unique chemical structure allows for the development of new compounds with improved efficacy and selectivity in controlling pests and diseases in agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 13306-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,0 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13306-99:
(7*1)+(6*3)+(5*3)+(4*0)+(3*6)+(2*9)+(1*9)=85
85 % 10 = 5
So 13306-99-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H7N3O2/c13-9(14)8-6-10-12(11-8)7-4-2-1-3-5-7/h1-6H,(H,13,14)/p-1
13306-99-5Relevant academic research and scientific papers
SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS
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, (2021/05/21)
The application relates to substituted hydantoinamides of formula (I) as ADAMTS7 antagonists, to processes for their preparation, their use alone or in combination for the treatment or prophylaxis of diseases, in particular of cardiovascular diseases, including atherosclerosis, coronary artery disease (CAD), peripheral vascular disease (PAD), arterial occlusive disease or restenosis after angioplasty. R1 is hydrogen, alkyl, cycloalkyl, heterocycloalkyl, 5- to 6-membered heteroaryl or phenyl; R2 is hydrogen or alkyl; A is 5-membered heteroaryl; Z is 6- to 10-membered aryl or 5- to 10-membered heteroaryl; all groups being optionally substituted.
Reactions of 1,2,3-triazoles with trifluoromethanesulfonyl chloride and trifluoromethanesulfonic anhydride
Meshcheryakov,Shainyan,Tolstikova,Albanov
, p. 1517 - 1521 (2007/10/03)
Reactions of 4,5-dibromo-1,2,3-triazole, 1H-1,2,3-benzotriazole, and 2-phenyl-2H-1,2,3-triazole-4-carbonyl chloride with trifluoromethanesulfonyl chloride and trifluoromethanesulfonic anhydride were studied. 4,5-Dibromo-1,2,3-triazole sodium salt reacted
