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23073-04-3

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23073-04-3 Usage

General Description

2,4-bis(4-methoxyphenyl)-4-oxobutanenitrile, also known as Bis(4-methoxyphenyl)-2,4-dioxobutanenitrile, is a chemical compound with the molecular formula C20H18N2O4. It is a yellow to orange solid that is insoluble in water but soluble in organic solvents. 2,4-bis(4-methoxyphenyl)-4-oxobutanenitrile is widely used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used in the research and development of new drugs and in the production of specialty chemicals. Additionally, it is known for its versatile reactivity and is commonly used in organic synthesis for the construction of complex molecular structures. However, it should be handled with care as it may cause irritation to the skin, eyes, and respiratory tract, and may be harmful if ingested or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 23073-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,7 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23073-04:
(7*2)+(6*3)+(5*0)+(4*7)+(3*3)+(2*0)+(1*4)=73
73 % 10 = 3
So 23073-04-3 is a valid CAS Registry Number.

23073-04-3SDS

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 2,4-bis(4-methoxyphenyl)-4-oxobutanenitrile

1.2 Other means of identification

Product number -
Other names 2,4-bis-(4-methoxy-phenyl)-4-oxo-butyronitrile

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:23073-04-3 SDS

23073-04-3Relevant articles and documents

Preparation of 3,5-diarylsubstituted 5-hydroxy-1,5-dihydro-2: H -pyrrol-2-ones via base-assisted cyclization of 3-cyanoketones

Aksenov, Nicolai A.,Aksenov, Dmitrii A.,Kurenkov, Igor A.,Aksenov, Alexander V.,Skomorokhov, Anton A.,Prityko, Lidiya A.,Rubin, Michael

, p. 16236 - 16245 (2021/05/19)

A convenient preparative method is developed allowing for expeditious assembly of 3,5-diarylsubstituted 5-hydroxy-1,5-dihydro-2H-pyrrol-2-ones from routinely available inexpensive synthetic precursors. These compounds could not be prepared via the previously known protocols, as 2-aminofuran derivatives were produced instead.

Discovery of a novel series of orally active non-peptide endothelin-A (ET(A)) receptor-selective antagonists

Doherty,Patt,Edmunds,Berryman,Reisdorph,Plummer,Shahripour,Lee,Cheng,Walker,Haleen,Keiser,Flynn,Welch,Hallak,Taylor,Reynolds

, p. 1259 - 1263 (2007/10/02)

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