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((2R,3S,5S)-3-(Benzoyloxy)-5-cyanotetrahydrofuran-2-yl)methyl benzoate is an organic compound with the molecular formula C21H19NO4. It is a derivative of benzoic acid and is composed of a tetrahydrofuran ring with a benzoyloxy and cyano substituent, and a benzoate ester group. This unique structure and functional groups make it a versatile molecule for various chemical reactions and biological studies.

127676-66-8

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127676-66-8 Usage

Uses

Used in Organic Synthesis:
((2R,3S,5S)-3-(Benzoyloxy)-5-cyanotetrahydrofuran-2-yl)methyl benzoate is used as an intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure and functional groups allow for a wide range of chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
((2R,3S,5S)-3-(Benzoyloxy)-5-cyanotetrahydrofuran-2-yl)methyl benzoate is used as a key component in pharmaceutical research for the development of new drugs. Its potential use in drug development and medicinal applications has attracted the attention of researchers, who are exploring its biological activity and potential therapeutic effects. ((2R,3S,5S)-3-(Benzoyloxy)-5-cyanotetrahydrofuran-2-yl)methyl benzoate's unique structure and functional groups make it a promising candidate for the design and synthesis of novel pharmaceutical agents.
Used in Drug Development:
((2R,3S,5S)-3-(Benzoyloxy)-5-cyanotetrahydrofuran-2-yl)methyl benzoate is used as a starting material in drug development for the creation of new therapeutic agents. Its unique structure and functional groups provide opportunities for the design of innovative drugs with improved efficacy, selectivity, and safety profiles. Researchers are actively investigating the compound's potential applications in various therapeutic areas, including oncology, neurology, and infectious diseases.
Used in Medicinal Applications:
((2R,3S,5S)-3-(Benzoyloxy)-5-cyanotetrahydrofuran-2-yl)methyl benzoate is used as a potential therapeutic agent in medicinal applications. Its unique structure and functional groups offer opportunities for the development of new treatments for various diseases and conditions. ((2R,3S,5S)-3-(Benzoyloxy)-5-cyanotetrahydrofuran-2-yl)methyl benzoate's potential use in drug development and medicinal applications has led to ongoing research and development efforts to fully understand its biological activity and therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 127676-66-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,7 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127676-66:
(8*1)+(7*2)+(6*7)+(5*6)+(4*7)+(3*6)+(2*6)+(1*6)=158
158 % 10 = 8
So 127676-66-8 is a valid CAS Registry Number.

127676-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,5S)-3-benzoyloxy-5-cyanooxolan-2-yl]methyl benzoate

1.2 Other means of identification

Product number -
Other names [(2R,3S,5S)-3-benzoyloxy-5-cyanooxolan-2-yl]methyl benzoate

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:127676-66-8 SDS

127676-66-8Relevant academic research and scientific papers

A Facile Preparative Method of C-Nucleosides

Togo, Hideo,Ishigami, Sachiko,Yokoyama, Masataka

, p. 1673 - 1676 (2007/10/02)

Facile and general preparative method of C-nucleosides has been achieved via 4 steps starting from 2-deoxy-D-ribose.The essential step in this method is the use of radical coupling reaction of 2-deoxy-D-ribofuranosyl radical derivative and some heteroaromatic bases.

Preparation of Modified Nucleosides from Glucosamine: Rapid and Efficient Formal Total Synthesis of Several 2'-Deoxy C-Nucleosides

Jung, Michael E.,Trifunovich, Ivan D.,Gardiner, John M.,Clevenger, Gary L.

, p. 84 - 85 (2007/10/02)

Formal total syntheses of several 2'-deoxy C-nucleosides have been accomplished in a short and efficient process using D-glucosamine as the starting material.

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