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Bis[4-(dimethylamino)phenyl]phosphinic acid is a complex organic compound with the chemical formula C16H20N2O2P. It is characterized by two 4-(dimethylamino)phenyl groups attached to a central phosphinic acid moiety. This molecule is known for its potential applications in various fields, including pharmaceuticals and materials science, where it may be used as a precursor or intermediate in the synthesis of more complex molecules. The presence of the dimethylamino groups contributes to its reactivity and solubility properties, making it a versatile building block in chemical synthesis.

7439-52-3

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7439-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7439-52-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,3 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7439-52:
(6*7)+(5*4)+(4*3)+(3*9)+(2*5)+(1*2)=113
113 % 10 = 3
So 7439-52-3 is a valid CAS Registry Number.

7439-52-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name bis[4-(dimethylamino)phenyl]phosphinic acid

1.2 Other means of identification

Product number -
Other names Tetramethyldiaminodiphenylphosphinsaeure

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:7439-52-3 SDS

7439-52-3Relevant academic research and scientific papers

Reaction of N-Arylsulfonyl-p-quinonimines and semiquinoid structures produced therefrom with Bis(p-dimethylaminophenyl)phosphinite

Avdeenko

, p. 1182 - 1190 (2007/10/03)

N-Arylsulfonyl-1,4-benzoquinonemonoimines react with bis(N-dimethylaminophenyl)phosphinite in keeping with the character and position of substituents in the quinoid ring along 1,4-, 6,1-, or 1,2-addition way; N-arylsulfonyl-1,4-naphthoquinonemonoimines react along 1,4-, 6,1-, 1,2-, or 6,3-addition. Semiquinoid polyhalostructures generated therefrom react similarly to the corresponding quinonimines possessing several chlorine substituents in the quinoid ring. N,N-Diarylsulfonyl-1,4-benzoquinonediimines with no substituents in the ring yield with bis(p-dimethylaminophenyl)phosphinite 1,4-addition products. Along a competing reaction quinonediimine is reduced to the corresponding phenylenediamine. With the tetrachloro substituted in the ring 1,4-benzoquinonediimine and the corresponding semiquinoid derivative only reduction is observed.

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