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54670-87-0

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54670-87-0 Usage

General Description

Diethyl 2-benzyl-3-oxosuccinate is a chemical compound with the molecular formula C17H20O5. It is a white to off-white crystalline powder that is commonly used as a reagent in organic synthesis. Diethyl 2-benzyl-3-oxosuccinate is a derivative of succinic acid and contains a benzyl group and a ketone functional group. Diethyl 2-benzyl-3-oxosuccinate is commonly employed in the preparation of various pharmaceutical intermediates and is also used in the production of fragrances and flavors. It is important to handle and store this compound with care, as it can be harmful if ingested or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 54670-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,7 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54670-87:
(7*5)+(6*4)+(5*6)+(4*7)+(3*0)+(2*8)+(1*7)=140
140 % 10 = 0
So 54670-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H18O5/c1-3-19-14(17)12(13(16)15(18)20-4-2)10-11-8-6-5-7-9-11/h5-9,12H,3-4,10H2,1-2H3

54670-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-benzyl-3-oxobutanedioate

1.2 Other means of identification

Product number -
Other names 2-benzyl diethyl oxaloacetate

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:54670-87-0 SDS

54670-87-0Relevant articles and documents

Ketoreductases in the synthesis of valuable chiral intermediates: Application in the synthesis of α-hydroxy β-amino and β-hydroxy γ-amino acids

Kambourakis, Spiros,Rozzell, J. David

, p. 663 - 669 (2007/10/03)

A general method for the synthesis of β-alkyl α-hydroxy β-amino and α- and γ-alkyl substituted β-hydroxy-γ- amino acids is described. The synthesis of all three classes of amino acids proceeds through a common chiral alcohol intermediate that is generated

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