15625-88-4 Usage
General Description
1H-1,2,4-Triazole,1-acetyl, also known as 1-acetyl-1H-1,2,4-triazole, is a chemical compound with the molecular formula C4H5N3O. It is a derivative of triazole and is commonly used in pharmaceuticals and agrochemicals. 1H-1,2,4-Triazole,1-acetyl-(6CI,7CI,8CI,9CI) has antifungal, anticancer, and antiviral properties, and is used in the synthesis of various pharmaceutical products. It is also used as a building block in organic chemistry for the synthesis of other complex compounds. Additionally, 1H-1,2,4-Triazole,1-acetyl is considered to be a potential mutagen and carcinogen, leading to it being regulated in some countries due to its toxic and hazardous nature.
Check Digit Verification of cas no
The CAS Registry Mumber 15625-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,2 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15625-88:
(7*1)+(6*5)+(5*6)+(4*2)+(3*5)+(2*8)+(1*8)=114
114 % 10 = 4
So 15625-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H5N3O/c1-4(8)7-3-5-2-6-7/h2-3H,1H3
15625-88-4Relevant articles and documents
N-Cyanazoles in Synthesis of Amides of Carboxylic Acids
Purygin,Pan'kov
, p. 871 - 873 (2007/10/03)
The reaction of carboxylic acids with 1-cyanimidazole, 1-cyanobenzimidazole, and 1-cyano-1,2,4-triazole leads to the formation of 1-acylazoles used in situ in synthesis of anilides of the corresponding carboxylic acids.
PHOTOCHEMISTRY OF N-ACYLAZOLES. VI). PHOTOREACTIVITIES OF 1-ACYL-1,2,4-TRIAZOLES AND OF 2-ACYLTETRAZOLES
Murato, Kazuo,Yatsunami, Takashi,Iwasaki, Shigeo
, p. 588 - 605 (2007/10/02)
Contrary to the findings in the photolysis of N-acylimidazoles (2) irradiation of 1-acyl-1,2,4-triazoles afforded no photo-Fries product, but instead products formed via the corresponding acyl radicals and aldehydes.Photolysis of 2-acyltetrazoles gave in part the same products as those obtained from the irradiation of the corresponding acyl-triazoles as well as 2-alkyl-1,3,4-oxadiazoles.N-Acyltetrazoles didn't give any photo-Fries product neither.
