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methyl 2-(4-methoxyphenyl)-4-oxo-4-phenyl-butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23073-05-4

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23073-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23073-05-4 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 23073-05:
(7*2)+(6*3)+(5*0)+(4*7)+(3*3)+(2*0)+(1*5)=74
74 % 10 = 4
So 23073-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O4/c1-21-15-10-8-13(9-11-15)16(18(20)22-2)12-17(19)14-6-4-3-5-7-14/h3-11,16H,12H2,1-2H3

23073-05-4SDS

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 methyl 2-(4-methoxyphenyl)-4-oxo-4-phenylbutanoate

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:23073-05-4 SDS

23073-05-4Relevant academic research and scientific papers

One-Pot Quinine-Catalyzed Synthesis of α-Chiral γ-Keto Esters: Enantioenriched Precursors of cis-α,γ-Substituted-γ-Butyrolactones

Meninno, Sara,Volpe, Chiara,Lattanzi, Alessandra

supporting information, p. 2845 - 2848 (2016/09/13)

A highly enantioselective one-pot synthesis of important building blocks, α-chiral γ-keto esters, has been developed by combining a quinine-catalyzed Michael addition of malononitrile to trans-enones followed by magnesium monoperoxyphthalate (MMPP) oxidat

Microwave assisted synthesis of 4,6-diarylpyridazin-3(2H)-ones in solid state

Meenakshi,Ramamoorthy,Muthusubramanian,Sivasubramanian

, p. 645 - 651 (2007/10/03)

Microwave assisted synthesis of dihydropyridazin-3(2H)-ones and the subsequent dehydrogenation using selenium dioxide are described.

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