138479-53-5 Usage
Description
2-[1,2,4]Triazol-1-yl-benzaldehyde is a chemical compound that belongs to a group of substances known as triazoles, which are characterized by their three nitrogen atoms and two carbon atoms arranged in a five-membered ring. This particular compound incorporates a benzaldehyde unit, known for its aromatic properties and role in the synthesis of other chemicals. The presence of the triazole ring and benzaldehyde group may suggest potential use in pharmaceuticals and materials science sectors, as many triazole derivatives are known to demonstrate a range of biological activities. Its exact properties, such as physical state, boiling point, and toxicity, would need to be determined experimentally.
Uses
Used in Pharmaceutical Industry:
2-[1,2,4]Triazol-1-yl-benzaldehyde is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its triazole ring and benzaldehyde group may contribute to the development of new drugs with potential biological activities.
Used in Materials Science:
2-[1,2,4]Triazol-1-yl-benzaldehyde is used as a building block in the creation of new materials with specific properties. The combination of the triazole ring and benzaldehyde group may lead to the development of materials with unique characteristics, such as improved stability or enhanced reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 138479-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,7 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138479-53:
(8*1)+(7*3)+(6*8)+(5*4)+(4*7)+(3*9)+(2*5)+(1*3)=165
165 % 10 = 5
So 138479-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H7N3O/c13-5-8-3-1-2-4-9(8)12-7-10-6-11-12/h1-7H
138479-53-5Relevant articles and documents
Cyclization Reactions in Azole Chemistry: The Reaction of Some Azoles with o-Fluoroacetophenone, o-Fluorobenzaldehyde and o-Fluorobenzophenone
Rosevear, Judi,Wilshire, John F. K.
, p. 1097 - 1114 (2007/10/02)
The reactions of some azoles with o-fluoro-acetophenone, -benzaldehyde and -benzophenone in dimethyl sulfoxide solution in the presence of anhydrous potassium carbonate have been investigated.In addition to the expected substitution products, cyclization