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3291-46-1

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3291-46-1 Usage

General Description

(2S,3S)-diethyl oxirane-2,3-dicarboxylate is a chemical compound with the molecular formula C8H12O6. It is also known by the systematic name diethyl (2S,3S)-2,3-epoxybutane-1,4-dicarboxylate. (2S,3S)-diethyl oxirane-2,3-dicarboxylate is a diester derived from oxirane and dicarboxylic acid. It is commonly used as an intermediate in organic synthesis to create other compounds, such as pharmaceuticals, agrochemicals, and fragrances. The (2S,3S) configuration indicates that the two chiral centers in the molecule have a specific 3-dimensional arrangement, which can impact its reactivity and biological activity. The compound's properties and potential applications make it a valuable building block in chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 3291-46-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3291-46:
(6*3)+(5*2)+(4*9)+(3*1)+(2*4)+(1*6)=81
81 % 10 = 1
So 3291-46-1 is a valid CAS Registry Number.

3291-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-(2S,3S)-trans-Oxiran-2,3-dicarbonsaeure-diethylester

1.2 Other means of identification

Product number -
Other names diethyl (2S,3S)-(+)-threo-2,3-epoxysuccinate

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:3291-46-1 SDS

3291-46-1Downstream Products

3291-46-1Relevant articles and documents

Approaching an experimental electron density model of the biologically active trans-epoxysuccinyl amide group—Substituent effects vs. crystal packing

Shi, Ming W.,Stewart, Scott G.,Sobolev, Alexandre N.,Dittrich, Birger,Schirmeister, Tanja,Luger, Peter,Hesse, Malte,Chen, Yu-Sheng,Spackman, Peter R.,Spackman, Mark A.,Grabowsky, Simon

, (2017)

The trans-epoxysuccinyl amide group as a biologically active moiety in cysteine protease inhibitors such as loxistatin acid E64c has been used as a benchmark system for theoretical studies of environmental effects on the electron density of small active i

2,3-EPOXY SUCCINYL DERIVATIVE, PREPARATION METHOD THEREFOR, AND USES THEREOF

-

Paragraph 0220; 0221; 0222, (2019/01/17)

The present invention relates to a 2,3-epoxy succinyl derivative, a preparation method and a use thereof, in particular, the present invention relates to a compound represented by Formula (1), a racemate or an optical isomer thereof, a solvate thereof, or

2, 3-Butanediamide Epoxide Compound and Preparation Method and Use Thereof

-

Paragraph 0161, (2016/05/19)

Provided are a compound of formula I which can be used as a drug against small RNA virus infections, and optical isomers, pharmaceutically acceptable salts, solvates or hydrates thereof. Also provided are the preparation method of the compound, the method for using the compound for treating bacterial infections and the use of the compound in the preparation of a drug for preventing and/or treating viral diseases caused by small RNA viruses.

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