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Acetonoxime-o-methylether, also known as o-methoxyiminoacetone or 2-methoxyimino-2-phenylacetonitrile, is an organic compound with the chemical formula C9H9NO. It is a colorless to pale yellow liquid that is soluble in organic solvents. Acetonoxim-o-methylether is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Acetonoxime-o-methylether is produced through the reaction of acetophenone with hydroxylamine and methanol, and it is known for its reactivity in various chemical transformations, making it a valuable building block in the chemical industry.

3376-35-0

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3376-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3376-35-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3376-35:
(6*3)+(5*3)+(4*7)+(3*6)+(2*3)+(1*5)=90
90 % 10 = 0
So 3376-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO/c1-4(2)5-6-3/h1-3H3

3376-35-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methoxypropan-2-imine

1.2 Other means of identification

Product number -
Other names Acetone oxime O-methylated

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3376-35-0 SDS

3376-35-0Relevant academic research and scientific papers

ASYMMETRICAL NONBRIDGEHEAD NITROGEN-XXVI SYNTHESIS, CONFIGURATIONALSTABILITY, AND RESOLUTION OF N,N-DIALKOXYAMINES INTO ANTIPODES

Konstyanovsky, Remir G.,Rudchenko, Vladimir F.,Shtamburg, Vasilii G.,Chervin, Ivan I.,Nasibov, Shahin S.

, p. 4245 - 4254 (2007/10/02)

Alkoxyamines with tertiary N-alkyl substituents were chlorinated to N-chloro-N-alkoxyamines whose reaction with alcohols enabled synthesis of N,N-dialkoxyamines.The DNMR method wos used to determine the barriers of of inversion of these compounds.Alkaline hydrolysis (13) followed by subsequent reactions with R-(+)- and S-(-)-a-phenylethylamine yielded diastereomeric salt (+29 and -29) whose crystallization and subsequent esterification resulted in optically active acyclic amines (-13 and +13) with the asymmetric center only at the N atom in the open chain.

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