138768-28-2 Usage
Description
N-(1 H-BENZOTRIAZOL-1-YLPHENYLMETHYL)-3-PYRIDINECARBOXAMIDE, also known as Benzotriazol-1-ylphenylmethyl-3-pyridinecarboxamide, is a chemical compound with a unique structure that features a benzotriazol-1-ylphenylmethyl group attached to a 3-pyridinecarboxamide moiety. N-(1 H-BENZOTRIAZOL-1-YLPHENYLMETHYL)-3-PYRIDINECARBOXAMIDE is characterized by its potential reactivity and versatility in chemical synthesis, making it a valuable intermediate for the preparation of various organic compounds.
Uses
Used in Chemical Synthesis:
N-(1 H-BENZOTRIAZOL-1-YLPHENYLMETHYL)-3-PYRIDINECARBOXAMIDE is used as an amidoalkylating reagent for the preparation of amidoalkylated products of aromatic and heterocyclic compounds. Its unique structure allows for the formation of new chemical bonds and the synthesis of a wide range of molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-(1 H-BENZOTRIAZOL-1-YLPHENYLMETHYL)-3-PYRIDINECARBOXAMIDE can be used as a key intermediate in the synthesis of novel drug candidates. Its ability to form amidoalkylated products with aromatic and heterocyclic compounds makes it a valuable tool for the development of new medications with improved pharmacological properties.
Used in Material Science:
In the field of material science, N-(1 H-BENZOTRIAZOL-1-YLPHENYLMETHYL)-3-PYRIDINECARBOXAMIDE may be utilized in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. Its unique structure and reactivity can contribute to the creation of advanced materials for various applications, including electronics, coatings, and adhesives.
Used in Research and Development:
N-(1 H-BENZOTRIAZOL-1-YLPHENYLMETHYL)-3-PYRIDINECARBOXAMIDE is also valuable in research and development settings, where it can be employed as a versatile building block for the synthesis of complex organic molecules. Its use in this context can lead to the discovery of new compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 138768-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,6 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138768-28:
(8*1)+(7*3)+(6*8)+(5*7)+(4*6)+(3*8)+(2*2)+(1*8)=172
172 % 10 = 2
So 138768-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H15N5O/c25-19(15-9-6-12-20-13-15)21-18(14-7-2-1-3-8-14)24-17-11-5-4-10-16(17)22-23-24/h1-13,18H,(H,21,25)
138768-28-2Relevant articles and documents
New N-mannich bases
Pernak,Weglewski,Szymanska
, p. 1135 - 1142 (2007/10/03)
Amides, aldehydes and benzotriazole or morpholine react, with the elimination of water to form N-Mannich bases or N,N′-arylidene symmetrical diamides in good or very good yields. We also found that amides, aldehydes and 1,2,4-triazole react to form a new N-[1-(1H-1,2,4-triazol-1-yl)alkyl]amides with a 58-85% yield.
