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2-(benzoylamino)-9-(3,5-di-O-benzoyl-2-deoxypentofuranosyl)-3,9-dihydro-6H-purin-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78763-67-4

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78763-67-4 Usage

Compound type

Complex chemical compound

Base component

Purine base

Derivative

Adenine derivative

Usage

Synthesis of nucleosides and nucleotides

Functional group

Benzoylamino group

Attachment position of the functional group

2-position of the purine ring

Additional groups

Two benzoyl groups

Attachment positions of additional groups

3 and 5 positions of the deoxyribose sugar

Potential applications

Pharmaceutical research, anti-cancer and antiviral drug development

Structural feature

Highly modified structure

Relevance

Interesting target for molecular design and drug discovery

Check Digit Verification of cas no

The CAS Registry Mumber 78763-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,6 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78763-67:
(7*7)+(6*8)+(5*7)+(4*6)+(3*3)+(2*6)+(1*7)=184
184 % 10 = 4
So 78763-67-4 is a valid CAS Registry Number.

78763-67-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Deoxy-L-ribose-anilide

1.2 Other means of identification

Product number -
Other names 2'-Deoxy-N2,3'-O-tribenzoylguanosine

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:78763-67-4 SDS

78763-67-4Downstream Products

78763-67-4Relevant academic research and scientific papers

Benzoyl cyanide: A mild and efficient reagent for benzoylation of nucleosides

Prasad, Ashok K.,Kumar, Vineet,Maity, Jyotirmoy,Wang, Zhiwei,Ravikumar, Vasulinga T.,Sanghvi, Yogesh S.,Parmar, Virinder S.

, p. 935 - 945 (2007/10/03)

Efficient benzoylation of various nucleosides has been accomplished in pyridine with a catalytic amount of DMAP and benzoyl cyanide under mild conditions.

Mild, efficient, selective and "green" benzoylation of nucleosides using benzoyl cyanide in ionic liquid

Prasad, Ashok K.,Kumar, Vineet,Maity, Jyotirmoy,Sanghvi, Yogesh S.,Ravikumar, Vasulinga T.,Parmar, Virinder S.

, p. 747 - 751 (2007/10/03)

Use of benzoyl cyanide (BzCN) for benzoylation of nucleosides has been studied, both in pyridine and in ionic liquid. BzCN in 1-methoxyethyl-3- methylimidazolium methanesulfonate as ionic liquid has been found to be a "green" alternative compared to the pyridine-BzCN system. An efficient and selective benzoylation of nucleosides of both, the 2′-deoxy- and the ribo-series at ambient temperature was accomplished. Copyright Taylor & Francis, Inc.

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