10300-21-7

Basic information

• Product Name: 1,2-Di-O-acetyl-5-Benzoyl-3-O-Methyl-D-ribofuranose
• Synonyms: 1,2-Di-O-acetyl-5-Benzoyl-3-O-Methyl-D-ribofuranose;D-Ribofuranose, 3-O-Methyl-, 1,2-diacetate 5-benzoate;1,2-Di-O-acetyl-5-benzoyl-3-O-Methyl-beta-D-ribofuranose;3-O-Methyl-D-ribofuranose 1,2-diacetate 5-benzoate
• CAS NO: 10300-21-7
• Molecular Formula: C17H20O8
• Molecular Weight: 352.3359
• Mol File: 10300-21-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-Di-O-acetyl-5-Benzoyl-3-O-Methyl-D-ribofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Di-O-acetyl-5-Benzoyl-3-O-Methyl-D-ribofuranose(10300-21-7)
• EPA Substance Registry System: 1,2-Di-O-acetyl-5-Benzoyl-3-O-Methyl-D-ribofuranose(10300-21-7)

Safety Data

• Hazardous Substances Data: 10300-21-7(Hazardous Substances Data)

Usage

General Description

1,2-Di-O-acetyl-5-Benzoyl-3-O-Methyl-D-ribofuranose is a chemical compound that belongs to the class of ribofuranose derivatives. It is a modified form of the sugar ribofuranose, with acetyl and benzoyl groups attached to its oxygen atoms. The methyl group is attached to the third carbon atom of the ribofuranose ring. 1,2-Di-O-acetyl-5-Benzoyl-3-O-Methyl-D-ribofuranose has potential applications in the fields of organic chemistry and pharmaceuticals due to its unique structure and properties. It may be used as a building block for the synthesis of other compounds or as a potential drug candidate. Overall, 1,2-Di-O-acetyl-5-Benzoyl-3-O-Methyl-D-ribofuranose is a chemically interesting molecule with possible industrial and medical applications.

Upstream product

• 108-24-7 acetic anhydride 
• 6612-91-5 ((3aR,5R,65,6aR)-6-hydroxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methyl benzoate 
• 10300-20-6 5-O-benzoyl-1,2-O-isopropylidene-3-O-methyl-α-D-ribofuranose 
• 64-19-7 acetic acid 
• 532-20-7 D-xylofuranose 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 6022-96-4 5-O-benzoyl-α-D-xylofuranose 
• 6698-46-0 5-O-benzoyl-1,2-O-isopropylidene-α-D-ribofuranos-3-ulose 
• 13035-61-5 1,2,3,5-tetraacetylribose 

Relevant articles and documents

MODIFIED CYCLIC DINUCLEOSIDE COMPOUNDS AS STING MODULATORS

Provided herein are compounds of Formula (I), Formula (II) and/or Formula (III), or pharmaceutically acceptable salts of any of the foregoing, pharmaceutical compositions that include a compound described herein (including pharmaceutically acceptable salt

Total synthesis of mycalisine B

The first total synthesis of the marine nucleoside Mycalisine B-a naturally occurring and structurally distinct 4,5-unsaturated 7-deazapurine nucleoside-has been accomplished in 10 linear steps with 27.5% overall yield from commercially available 1,2,3,5-tetra-O-acetyl-ribose and tetracyanoethylene. Key steps of the approach include: (1) I2 catalyzed acetonide formation from 1,2,3,5-tetra-O-acetylribose and acetone at large scale; (2) Vorbrüggen glycosylation using N4-benzoyl-5-cyano-6-bromo-7H-pyrrolo[2,3-d]pyrimidine as a nucleobase to avoid formation of N-3 isomer; (3) mild and scalable reaction conditions.

A total synthesis of mycalisine A

In this paper, we report a total synthesis of a naturally occurring pyrrolo[2,3-d]pyrimidine nucleoside, mycalisine A. Our synthetic strategy uses d-xylose as the starting material and Vorbrüggen glycosylation as the key step. Mycalisine A was synthesized in 11 steps with a 15% overall yield.