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16434-48-3

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16434-48-3 Usage

General Description

2-C-Methyl-1,3,5-tri-O-benzoyl-alpha-D-ribofuranoside is a chemical compound that is a derivative of ribose, a natural sugar found in RNA. It is often used in organic chemistry as a building block for the synthesis of more complex molecules. 2-C-Methyl-1,3,5-tri-O-benzoyl-alpha-D-ribofuranoside is a ribofuranoside, meaning it contains a furanose ring, and is substituted with three benzoyl groups and a methyl group at the 2-C position. These modifications can alter the compound's reactivity and stability, making it useful for various chemical reactions and processes. Its specific properties and reactivity make 2-C-Methyl-1,3,5-tri-O-benzoyl-alpha-D-ribofuranoside valuable in the field of organic synthesis and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 16434-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,3 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16434-48:
(7*1)+(6*6)+(5*4)+(4*3)+(3*4)+(2*4)+(1*8)=103
103 % 10 = 3
So 16434-48-3 is a valid CAS Registry Number.

16434-48-3SDS

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,4S)-3,5-dibenzoyloxy-4-hydroxy-4-methyloxolan-2-yl]methyl benzoate

1.2 Other means of identification

Product number -
Other names 2-C-Methyl-1,3,5-tri-O Cbenzoyl-|A-D-ribofuranoside

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:16434-48-3 SDS

16434-48-3Relevant articles and documents

2′-C-alkylribonucleosides: Design, synthesis, and conformation

Harry-O'kuru, Rogers E.,Kryjak, Emily A.,Wolfe, Michael S.

, p. 1457 - 1460 (2007/10/03)

Certain 2′-C-alkylribonucleotides have been designed as potential mechanism-based inactivators of ribonucleotide reductases. A short, flexible route toward the corresponding nucleosides and NMR evidence concerning their preferred solution conformations are discussed. Copyright

A concise synthesis of 2'-C-methylribonucleosides

Wolfe,Harry-O'kuru

, p. 7611 - 7614 (2007/10/02)

2'-C-methylribonucleosides were synthesized in five steps from commercially available 1,3,5-tri-O-benzoyl-α-D-ribose with good overall yields.

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