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13937-08-1

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13937-08-1 Usage

General Description

DIETHYL 2-HYDROXYMALONATE is a chemical compound that is commonly used in organic synthesis and pharmaceutical manufacturing. It is an ester derivative of malonic acid and contains two ethyl groups attached to the malonate backbone. DIETHYL 2-HYDROXYMALONATE is known for its ability to undergo various chemical reactions, including ester hydrolysis and decarboxylation, making it a versatile building block in the synthesis of complex organic molecules. DIETHYL 2-HYDROXYMALONATE has also been reported to exhibit antioxidant and anti-inflammatory properties, and it is being studied for potential therapeutic applications in the field of medicine. However, as with any chemical compound, proper handling and safety precautions should be followed when working with DIETHYL 2-HYDROXYMALONATE.

Check Digit Verification of cas no

The CAS Registry Mumber 13937-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,3 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13937-08:
(7*1)+(6*3)+(5*9)+(4*3)+(3*7)+(2*0)+(1*8)=111
111 % 10 = 1
So 13937-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O5/c1-3-11-6(9)5(8)7(10)12-4-2/h5,8H,3-4H2,1-2H3

13937-08-1SDS

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-hydroxypropanedioate

1.2 Other means of identification

Product number -
Other names diethyl hydroxymalonate

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:13937-08-1 SDS

13937-08-1Relevant articles and documents

Photoredox-Enabled Synthesis of β-Substituted Pyrroles from Pyrrolidines

An, Xiao-De,Yang, Shuo,Qiu, Bin,Yang, Ting-Ting,Li, Xian-Jiang,Xiao, Jian

, p. 9558 - 9565 (2020)

The merger of photoredox-initiated enamine-imine tautomerization and nucleophilic addition processes to access β-substituted pyrroles from pyrrolidines has been achieved. The significant advantage of this method is suppressing the Friedel-Crafts reaction,

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