90476-10-1 Usage
Uses
Used in Organic Synthesis:
[(2E)-1-methyl-3-(4-nitrophenyl)triaz-2-en-1-yl]methyl acetate is used as a building block in organic synthesis for the creation of a wide range of compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable component in the development of new molecules with specific properties and applications.
Used in Pharmaceutical Production:
In the pharmaceutical industry, [(2E)-1-methyl-3-(4-nitrophenyl)triaz-2-en-1-yl]methyl acetate is used as a key intermediate in the synthesis of various drugs. Its incorporation into drug molecules can contribute to enhanced biological activities, potentially leading to the development of novel therapeutics.
Used in Agrochemical Development:
Similarly, in the agrochemical sector, [(2E)-1-methyl-3-(4-nitrophenyl)triaz-2-en-1-yl]methyl acetate serves as a crucial component in the synthesis of compounds with pesticidal, herbicidal, or fungicidal properties. Its integration into these chemicals can improve their effectiveness in protecting crops and managing pests.
Used in Medicinal Chemistry Research:
Due to its potential biological activities, [(2E)-1-methyl-3-(4-nitrophenyl)triaz-2-en-1-yl]methyl acetate is also utilized in the field of medicinal chemistry as a subject of research. Scientists explore its interactions with biological targets to understand its possible therapeutic applications and to design new drugs based on its structure.
Safety Precautions:
Given its potential toxicity, [(2E)-1-methyl-3-(4-nitrophenyl)triaz-2-en-1-yl]methyl acetate should be handled with care. It is essential to work in a well-ventilated area and use appropriate personal protective equipment to minimize health risks during its use in research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 90476-10-1 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 90476-10:
(7*9)+(6*0)+(5*4)+(4*7)+(3*6)+(2*1)+(1*0)=131
131 % 10 = 1
So 90476-10-1 is a valid CAS Registry Number.
90476-10-1Relevant 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.
