90476-08-7 Usage
Description
[(2E)-3-(4-cyanophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate is an organic compound that belongs to the class of acetates. It is characterized by a molecular structure containing a 4-cyanophenyl group and a triaz-2-en-1-yl group, with a methyl acetate moiety. This chemical is known for its potential applications in various industries, particularly in the synthesis of other organic compounds and as an intermediate in the production of pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
[(2E)-3-(4-cyanophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate is used as an intermediate for the synthesis of various pharmaceutical compounds. Its unique molecular structure allows it to serve as a building block in the development of new drugs, potentially contributing to the treatment of various medical conditions.
Used in Chemical Synthesis:
In the chemical industry, [(2E)-3-(4-cyanophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate is used as a reagent in the synthesis of other organic compounds. Its versatile structure enables it to participate in various chemical reactions, leading to the creation of a wide range of products with different applications.
Used in Research and Development:
[(2E)-3-(4-cyanophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate is also utilized in research and development settings, where it can be studied for its properties and potential applications. Scientists and researchers may use [(2E)-3-(4-cyanophenyl)-1-methyltriaz-2-en-1-yl]methyl acetate to explore new chemical reactions, develop novel materials, or investigate its interactions with other substances.
Check Digit Verification of cas no
The CAS Registry Mumber 90476-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,7 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90476-08:
(7*9)+(6*0)+(5*4)+(4*7)+(3*6)+(2*0)+(1*8)=137
137 % 10 = 7
So 90476-08-7 is a valid CAS Registry Number.
90476-08-7Relevant articles and documents
OPEN-CHAIN NITROGEN COMPOUNDS. PART V. HYDROXYMETHYLTRIAZENES: SYNTHESIS OF SOME NEW ALKYL HOMOLOGUES OF THE ANTI-TUMOUR 3-METHYL-3-HYDROXYMETHYLTRIAZENES AND PREPARATION OF THE DERIVED ACETOXYMETHYL-, BENZOYLOXYMETHYL-, AND METHOXYMETHYLTRIAZENES
Hemens, Chantal M.,Manning, Hartford W.,Vaughan, Keith,LaFrance, Ronald,Tang, York
, p. 741 - 748 (2007/10/02)
The synthesis of some new 1-aryl-3-alkyl-3-hydroxymethyltriazenes is described.The method of coupling a diazonium salt with an alkylamine/formaldehyde mixture has been extended to (a) some diazonium ions with para substituents other than -M groups, (b) those with substituents in ortho position, and (c) to homologous alkylamines (e.g. ethylamine, propylamine, etc.).Hydroxymethyltriazenes can also be prepared by the reaction of a 1-aryl-3-methyltriazene with formaldehyde.Several new derivatives of hydroxymethyl function have been prepared.Reaction with acetic anhydride or benzoyl chloride in pyridine affords respectively the acetoxymethyl- and benzoyloxymethyl-triazenes; the acetates and benzoates react readily with methanol to give the novel methoxymethyltriazenes.This is the first report of a series of dialkyltriazenes with an ether linkage in the α position. An ether of this type has also been obtained directly from the diazonium fluoroborate salt by coupling with a mixture of benzylamine and formaldehyde in ethanolic solution.
