90476-21-4 Usage
Uses
Used in Organic Synthesis:
(1E)-1-(4-bromophenyl)-3-(methoxymethyl)-3-methyltriaz-1-ene is used as a synthetic intermediate for the creation of more complex organic molecules, leveraging its reactive sites for chemical transformations.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (1E)-1-(4-bromophenyl)-3-(methoxymethyl)-3-methyltriaz-1-ene is used as a potential lead compound for the development of new drugs, given its unique structural features that may offer novel therapeutic properties.
Used in Materials Science:
(1E)-1-(4-bromophenyl)-3-(methoxymethyl)-3-methyltriaz-1-ene is utilized in the field of materials science for the design and synthesis of new materials with specific properties, such as those with potential applications in coatings, adhesives, or other industrial materials.
Used in Medical Research:
In medicine and pharmacology, (1E)-1-(4-bromophenyl)-3-(methoxymethyl)-3-methyltriaz-1-ene is studied for its possible biological activities, which may lead to its use in therapeutic applications or as a tool in understanding certain biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 90476-21-4 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, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90476-21:
(7*9)+(6*0)+(5*4)+(4*7)+(3*6)+(2*2)+(1*1)=134
134 % 10 = 4
So 90476-21-4 is a valid CAS Registry Number.
90476-21-4Relevant 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.
