90476-11-2 Usage
Uses
Used in Pharmaceutical Industry:
[(2E)-3-(4-acetylphenyl)-1-methyltriaz-2-en-1-yl]methyl acetate is used as an intermediate in the synthesis of various biologically active compounds. Its unique structure and reactivity contribute to the development of new pharmaceuticals with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, [(2E)-3-(4-acetylphenyl)-1-methyltriaz-2-en-1-yl]methyl acetate is utilized as a key component in the creation of compounds with pesticidal or herbicidal properties. Its incorporation into these products can enhance their effectiveness in protecting crops and managing pests.
Used in Material Science:
[(2E)-3-(4-acetylphenyl)-1-methyltriaz-2-en-1-yl]methyl acetate may have potential applications in the field of material science due to its unique structure. It could be used in the development of novel materials with specific properties, such as improved strength, durability, or chemical resistance.
Used in Organic Chemistry:
This chemical also holds promise in the field of organic chemistry, where it can be employed as a building block or reactant in the synthesis of complex organic molecules. Its reactivity and structural features make it a valuable tool for chemists working on advanced organic compounds.
It is important to handle [(2E)-3-(4-acetylphenyl)-1-methyltriaz-2-en-1-yl]methyl acetate with care and take necessary precautions due to its potential hazards and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 90476-11-2 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, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90476-11:
(7*9)+(6*0)+(5*4)+(4*7)+(3*6)+(2*1)+(1*1)=132
132 % 10 = 2
So 90476-11-2 is a valid CAS Registry Number.
90476-11-2Relevant academic research and scientific papers
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.
