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145416-96-2

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145416-96-2 Usage

Description

1,3,5-Tri-O-benzoyl-2-deoxyribofuranose, with the CAS number 145416-96-2, is a white solid compound that is particularly useful in the field of organic synthesis. It is a derivative of 2-deoxyribofuranose, a sugar molecule that is part of the backbone of DNA. The benzoyl groups attached to the 1, 3, and 5 positions of the molecule provide unique chemical properties that make it valuable for various applications in organic chemistry.

Uses

Used in Organic Synthesis:
1,3,5-Tri-O-benzoyl-2-deoxyribofuranose is used as an intermediate in organic synthesis for the production of various complex organic compounds. Its unique structure and reactivity make it a versatile building block for the creation of a wide range of molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,3,5-Tri-O-benzoyl-2-deoxyribofuranose is used as a key component in the synthesis of novel drug candidates. Its unique chemical properties allow for the development of new molecules with potential therapeutic applications, such as antibiotics, antiviral agents, and anticancer drugs.
Used in Research and Development:
1,3,5-Tri-O-benzoyl-2-deoxyribofuranose is also used in research and development laboratories for the study of various chemical reactions and mechanisms. Its unique structure provides a valuable tool for understanding the reactivity of different functional groups and the development of new synthetic strategies.
Used in Material Science:
In the field of material science, 1,3,5-Tri-O-benzoyl-2-deoxyribofuranose can be used as a component in the development of new materials with specific properties. Its unique chemical structure can be exploited to create materials with tailored properties, such as improved stability, enhanced reactivity, or specific interactions with other molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 145416-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,4,1 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 145416-96:
(8*1)+(7*4)+(6*5)+(5*4)+(4*1)+(3*6)+(2*9)+(1*6)=132
132 % 10 = 2
So 145416-96-2 is a valid CAS Registry Number.
InChI:InChI=1/C26H22O7/c27-24(18-10-4-1-5-11-18)30-17-22-21(32-25(28)19-12-6-2-7-13-19)16-23(31-22)33-26(29)20-14-8-3-9-15-20/h1-15,21-23H,16-17H2/t21?,22-,23?/m1/s1

145416-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-Tri-O-benzoyl-2-deoxyribofuranose

1.2 Other means of identification

Product number -
Other names [(2R)-3,5-dibenzoyloxyoxolan-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:145416-96-2 SDS

145416-96-2Relevant articles and documents

Synthesis of C-Nucleosides via Radical Coupling Reaction

Togo, Hideo,Ishigami, Sachiko,Fujii, Misa,Ikuma, Toshihiro,Yokoyama, Masataka

, p. 2931 - 2942 (2007/10/02)

Photolysis of O-acyl derivatives of N-hydroxy-2-thiopyridone, prepared from tetrahydrofuran-2-carboxylic acid, D-ribofuranosylmethanoic acid, and D-ribopyranosylmethanoic acid, gave the corresponding C-nucleoside derivatives in the presence of heteroaromatic compounds via radical pathways.The essential step in this method is a radical coupling reaction of D-ribofuranosyl radical or D-ribopyranosyl radical and some heteroaromatic bases.This is a new method for the preparation of C-nucleosides using sugar carboxylic acids.

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