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6698-46-0

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6698-46-0 Usage

Description

5-O-Benzoyl-1,2-O-isopropylidene-alpha-D-erythro-pent-3-ulofuranose is a chemical compound that serves as a key intermediate in the synthesis of various biologically active molecules. It is characterized by the presence of a benzoyl group at the 5-O position and an isopropylidene protecting group at the 1,2-O positions, with the alpha-D-erythro-pent-3-ulose core structure.

Uses

Used in Pharmaceutical Industry:
5-O-Benzoyl-1,2-O-isopropylidene-alpha-D-erythro-pent-3-ulofuranose is used as a key intermediate in the chemical synthesis of D-ribose, an essential component of nucleic acids and various other biological molecules. Its role in the synthesis process is crucial for the production of pharmaceuticals and other healthcare products.
Used in Biochemistry Research:
5-O-Benzoyl-1,2-O-isopropylidene-alpha-D-erythro-pent-3-ulofuranose is also utilized in the preparation of methylated nucleoside derivatives, which are important for studying the structure and function of nucleic acids and their interactions with proteins. The synthesis of these derivatives contributes to a better understanding of molecular biology and the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 6698-46-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,9 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6698-46:
(6*6)+(5*6)+(4*9)+(3*8)+(2*4)+(1*6)=140
140 % 10 = 0
So 6698-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O6/c1-15(2)20-12-11(16)10(19-14(12)21-15)8-18-13(17)9-6-4-3-5-7-9/h3-7,10,12,14H,8H2,1-2H3

6698-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2-dimethyl-6-oxo-3a,6a-dihydrofuro[2,3-d][1,3]dioxol-5-yl)methyl benzoate

1.2 Other means of identification

Product number -
Other names 5-O-Benzoyl-1,2-O-(1-methylethylidene)pentofuranos-3-ulose

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:6698-46-0 SDS

6698-46-0Relevant articles and documents

Stereoselective synthesis of new higher carbon sugars from D-xylose

Liu, Hong-Min,Zou, Da-Peng,Zhang, Fuyi,Zhu, Wei-Guo,Peng, Tao

, p. 2103 - 2106 (2004)

A simple, one-pot multi-step route for the synthesis of a higher carbon sugar 3 by the HDA reaction of a α,β-unsaturated ketone prepared in situ from protected D-xylose with PDC in C6H6 or CH 3CN, followed by the reduction

CYCLIC DINUCLEOTIDES AS STING AGONISTS

-

, (2021/01/29)

Disclosed herein are cyclic di-nucleotide compounds and derivatives thereof that may be useful as STING agonists, and a pharmaceutical composition comprising the same. Also disclosed herein is the process for synthesis and to uses of such cyclic di-nucleo

SYNTHESIS OF 1,2,5-TRI-0-BENZ0YL-3-DIBENZYLAMIN0-3-DE0XYRIB0SE AS INTERMEDIATE FOR PRODUCING 3'-AMINO-3'-DEOXYADENOSINE AND 3'-AMINO-3'-DEOXYGUANOSINE AND THE PROTECTED DERIVATIVES THEREOF

-

, (2020/08/22)

The invention generally relates to improved processes for the preparation of intermediates of a cyclic dinucleotide which is useful as a STING agonist.

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