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2-(2-CHLORO-4-NITROPHENYL)-N,N-DIMETHYLETHENAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85544-62-3

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85544-62-3 Usage

Physical form

Yellow crystalline solid

Molecular weight

239.67 g/mol

Solubility

Soluble in organic solvents

Melting point

185-187°C

Uses

Synthetic dye intermediate in the production of various organic compounds, including pharmaceuticals and agrochemicals

Chemical properties

Unique reactivity as a precursor in the synthesis of various dyes and other organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 85544-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,4 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85544-62:
(7*8)+(6*5)+(5*5)+(4*4)+(3*4)+(2*6)+(1*2)=153
153 % 10 = 3
So 85544-62-3 is a valid CAS Registry Number.

85544-62-3SDS

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 2-(2-CHLORO-4-NITROPHENYL)-N,N-DIMETHYLETHENAMINE

1.2 Other means of identification

Product number -
Other names -

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:85544-62-3 SDS

85544-62-3Relevant academic research and scientific papers

Facile, environmentally friendly synthesis of benzaldehyde and phenylacetaldehyde analogs from readily available toluene derivatives

Dai, Liyan,Yu, Jie,Chen, Yingqi,Yu, Shichao

scheme or table, p. 3078 - 3084 (2011/09/14)

A facile environmentally friendly synthesis of bezaldehyde and phenylacetaldehyde analogs from readily available toluene derivatives is described. Oxidation of the styrylamines by H2O2 H2O2 affords benzaldehydes in moderate yields, while the hydrolysis of styrylamines afforded phenylacetaldehyde analogs in good yields. Copyright

REACTION OF GOLD'S REAGENT WITH ACTIVATED METHYLENE GROUPS DERIVED FROM ESTERS AND NITROARENES

Gupton, John T.,Lizzi, Michael J.,Polk, Dale

, p. 939 - 946 (2007/10/02)

A series of esters and nitrotoluenes were reacted with Gold's reagent under basic conditions and were found to produce the corresponding dimethylamino methyleneated product in both cases.

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