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922-68-9

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922-68-9 Usage

Uses

Methyl Glyoxylate is a useful compound for preparation of pyridine and quinoline derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 922-68-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 922-68:
(5*9)+(4*2)+(3*2)+(2*6)+(1*8)=79
79 % 10 = 9
So 922-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H4O3/c1-6-3(5)2-4/h2H,1H3

922-68-9SDS

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 Methyl Glyoxylate

1.2 Other means of identification

Product number -
Other names Methyl 2-oxoacetate

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:922-68-9 SDS

922-68-9Relevant articles and documents

Indium-mediated diastereoselective allylation of N-tert-butanesulfinyl imines derived from α-ketoesters

Maciá, Edgar,Foubelo, Francisco,Yus, Miguel

, p. 6001 - 6010 (2016)

The indium-mediated allylation of α-aldimino and -ketimino esters 3 with allylic bromides proceeds with high diastereoselectivity to yield homoallylic α-amino ester derivatives 5, in both THF and water as solvents. The reactions are diastereospecific, the stereochemical outcome depending on the configuration of both the sulfur atom of the sulfinyl group and the C[dbnd]N double bond. Of particular interest are the reaction products using ethyl bromomethylacrylate as allylating reagent because amino diesters are obtained, which can be easily transformed into enantiomerically pure α-methylidene-γ-butyrolactams 6 with an alkoxycarbonyl group on the ring bearing the nitrogen atom.

An Economical Route to Lamivudine Featuring a Novel Strategy for Stereospecific Assembly

Abdiaj, Irini,Ahmad, Saeed,Burns, Justina M.,Gopalsamuthiram, Vijayagopal,Gupton, B. Frank,Krack, Rudy,McQuade, D. Tyler,Nelson, Ryan C.,Snead, David R.,Stringham, Rodger W.

supporting information, p. 1194 - 1198 (2020/07/15)

An economical synthesis of lamivudine was developed by employing a new method to establish the stereochemistry about the heterocyclic oxathiolane ring. Toward this end, an inexpensive and readily accessible lactic acid derivative served the dual purpose of activating the carbohydrate's anomeric center for N-glycosylation and transferring stereochemical information to the substrate simultaneously. Both enantiomers of the lactic acid derivative are available, and either β-enantiomer in this challenging class of 2′-deoxynucleoside active pharmaceutical ingredients can be formed.

Method for producing glyoxylate through oxidation of glycollate

-

Paragraph 0080; 0081; 0082; 0083; 0084; 0085; 0086-0131, (2017/12/30)

The invention relates to a method for producing glyoxylate through oxidation of glycollate. The invention mainly aims to overcome the problem of low yield of glyoxylate in the prior art. The method provided by the invention comprises a reaction step of contacting a nitrogen oxide and oxygen-containing gas with glycollate to produce glyoxylate. A catalyst used in the invention comprises the following components by weight: a) 0.5 to 30 parts of at least one active component selected from a group consisting of iron and iron oxides; b) 0 to 10 parts of an auxiliary agent which is at least one metal selected from a group consisting of group IA or group IIA elements or oxides thereof; and c) 70 to 99 parts of a carrier. With such a technical scheme, the above problem is overcome, and the method is applicable to industrial production of glyoxylate through oxidation of glycollate.

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