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74213-59-5

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74213-59-5 Usage

General Description

"(2R,3R)-diethyl 2-acetoxy-3-bromosuccinate" is a chemical compound with the molecular formula C10H16O6Br. It is a derivative of succinic acid and is known for its acetoxy and bromo functional groups. (2R,3R)-diethyl 2-acetoxy-3-broMosuccinate is commonly used in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. It is also used in research and development for its potential biological and pharmacological activities. Additionally, it is a valuable reagent for the preparation of chiral building blocks and other compounds with specific stereochemical characteristics. Overall, "(2R,3R)-diethyl 2-acetoxy-3-bromosuccinate" is a versatile compound with various applications in the fields of chemistry and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 74213-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,1 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74213-59:
(7*7)+(6*4)+(5*2)+(4*1)+(3*3)+(2*5)+(1*9)=115
115 % 10 = 5
So 74213-59-5 is a valid CAS Registry Number.

74213-59-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-Diethyl 2-acetoxy-3-bromosuccinate

1.2 Other means of identification

Product number -
Other names diethyl (2R,3R)-2-acetyloxy-3-bromobutanedioate

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:74213-59-5 SDS

74213-59-5Relevant articles and documents

An improved preparation of the activity-based probe JPM-OEt and in situ applications

Chehade, Kareem A. H.,Baruch, Amos,Verhelst, Steven H. L.,Bogyo, Matthew

, p. 240 - 244 (2007/10/03)

A short, stereoselective synthesis of the general, cell permeable cathepsin probe JPM-OEt, is presented. The synthetic route is improved and described in more detail than previous reports for related compounds. This serves as a facile method for the synth

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