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(2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate) is a synthetic derivative of D-erythro-pentonic acid-g-lactone, a precursor to various important bioactive compounds. (2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate) is characterized by the presence of two fluorine atoms, two methyl groups, and two 4-chlorobenzoate groups attached to the 3 and 5 positions of the pentonic acid-g-lactone. The incorporation of these chemical features, such as fluorine and methyl groups, can enhance the metabolic stability and pharmacokinetic properties of drugs, while the 4-chlorobenzoate groups facilitate easy detection and purification of the compound. This makes (2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate) a promising candidate for applications in medicinal chemistry and drug development.

1294481-79-0

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1294481-79-0 Usage

Uses

Used in Medicinal Chemistry:
(2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate) is used as a building block for the synthesis of novel bioactive compounds due to its unique chemical structure and functional groups.
Used in Drug Development:
(2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate) is used as a potential pharmaceutical candidate for the development of new drugs, given its improved metabolic stability and pharmacokinetic properties conferred by the fluorine and methyl groups.
Used in Detection and Purification:
(2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate) is used as a compound with enhanced detection and purification capabilities in chemical and pharmaceutical processes, thanks to the presence of the 4-chlorobenzoate groups.
Further research into the biological activity and potential pharmaceutical applications of (2R)-2-Deoxy-2-fluoro-2-Methyl-D-erythro-pentonic acid-g-lactone 3,5-bis(4-chlorobenzoate) is warranted to fully explore its potential in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1294481-79-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,4,4,8 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1294481-79:
(9*1)+(8*2)+(7*9)+(6*4)+(5*4)+(4*8)+(3*1)+(2*7)+(1*9)=190
190 % 10 = 0
So 1294481-79-0 is a valid CAS Registry Number.

1294481-79-0SDS

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 [(2R,3R,4R)-3-(4-chlorobenzoyl)oxy-4-fluoro-4-methyl-5-oxooxolan-2-yl]methyl 4-chlorobenzoate

1.2 Other means of identification

Product number -
Other names ERY011

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:1294481-79-0 SDS

1294481-79-0Relevant academic research and scientific papers

The synthesis of hydroxyaminopurine nucleosied (by machine translation)

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Paragraph 0213, (2016/10/10)

A compound or salt thereof having the following structure useful for the treatment of hepatitis C virus (HCV): wherein R 7 is C 1-6 alkyl or C 3-6 cycloalkyl and R 8 is -O(C 1-6 alkyl) or -O(C 3-6 cycloalkyl).

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