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DIETHYL OXALATE-13C2 is a chemical compound that is labeled with two 13C isotopes, which makes it a useful tool in various chemical and biological research applications. It is an ethyl ester derivative of oxalic acid and is known for its unique properties that can be exploited in different fields.

150992-84-0

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150992-84-0 Usage

Uses

Used in Pharmaceutical Industry:
DIETHYL OXALATE-13C2 is used as a synthetic intermediate for the development of novel indole β-diketo acid derivatives. These derivatives have potential applications as HIV-1 integrase inhibitors, which are crucial in the treatment and management of HIV/AIDS. The compound plays a vital role in the synthesis process, contributing to the creation of effective antiretroviral drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 150992-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,9,9 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 150992-84:
(8*1)+(7*5)+(6*0)+(5*9)+(4*9)+(3*2)+(2*8)+(1*4)=150
150 % 10 = 0
So 150992-84-0 is a valid CAS Registry Number.

150992-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl oxalate

1.2 Other means of identification

Product number -
Other names Diethyl oxalate-13C2

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:150992-84-0 SDS

150992-84-0Downstream Products

150992-84-0Relevant academic research and scientific papers

Chemoenzymatic Synthesis of 13C-Labeled S-(-)-Malic Acid

Hillner, A.C.,Jans, A.W.H.,Winkel, C.

, p. 332 - 336 (1993)

The first regio- and stereospecific synthesis of S-(-)-13C-malic acid 5 with a high incorporation of 13C and excellent enantiomeric excess is described.S-(-)-13C-malic acid 5 was synthesized in a three-step reaction starting with ethyl acetate 2 and diethyl oxalate 1.The produced sodium diethyl oxaloacetate 3 was then enantioselectively reduced with bakers yeast to S-(-)-13C-malic acid diethylester 4 which was hydrolyzed to S-(-)-13C-malic acid 5.

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