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(E)-2-(2-methoxyphenyl)acetaldehyde oxime is an organic compound with the molecular formula C9H11NO2. It is a derivative of acetaldehyde, featuring a 2-methoxyphenyl group attached to the double-bonded carbon. This oxime is formed by the reaction of acetaldehyde with hydroxylamine, resulting in the addition of an OH group to the carbonyl carbon and an NH2 group to the adjacent carbon. The compound is characterized by its aldehyde group, which is responsible for its strong, pungent odor. It is used in the synthesis of various pharmaceuticals and chemical intermediates, and is also known for its potential applications in the fragrance industry due to its unique scent profile.

82204-36-2

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82204-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82204-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,0 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82204-36:
(7*8)+(6*2)+(5*2)+(4*0)+(3*4)+(2*3)+(1*6)=102
102 % 10 = 2
So 82204-36-2 is a valid CAS Registry Number.

82204-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2-(2-methoxyphenyl)acetaldehyde oxime

1.2 Other means of identification

Product number -
Other names (2-Methoxy-phenyl)-acetaldehyd-oxim

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:82204-36-2 SDS

82204-36-2Downstream Products

82204-36-2Relevant academic research and scientific papers

New approach to oximes through reduction of nitro compounds enabled by visible light photoredox catalysis

Cai, Shunyou,Zhang, Shaolong,Zhao, Yaohong,Wang, David Zhigang

, p. 2660 - 2663 (2013/07/11)

A range of nitro compounds are smoothly reduced to their corresponding oximes under the synergistic effects of visible light irradiation, the Ru(bpy)3Cl2 photocatalyst, Hünig's base, Mg(ClO 4)2 activation, and MeCN solvent. This remarkably mild and environmentally benign protocol, when orchestrated with classical Beckmann rearrangement, enables such high-value industrial feedstock as caprolactam to be readily accessed from simple precursor nitrocyclohexane.

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