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N-acetyl-9-(3,5-di-O-acetyl-2-deoxypentofuranosyl)-9H-purin-6-amine, also known as 3',5'-di-O-acetyl-N2-acetyl-2'-deoxyguanosine, is a complex organic compound with the molecular formula C18H22N6O8. It is a derivative of the nucleoside deoxyguanosine, where the 2'-hydroxyl group is replaced by a hydrogen atom, and the guanine base is acetylated at the N2 position. Additionally, the 3' and 5' positions of the deoxyribose sugar are acetylated, which protects the hydroxyl groups and can be important for stability and reactivity in chemical synthesis. N-acetyl-9-(3,5-di-O-acetyl-2-deoxypentofuranosyl)-9H-purin-6-amine is of interest in the field of biochemistry and medicinal chemistry, particularly in the study of nucleic acid analogs and their potential applications in drug development and understanding the mechanisms of DNA and RNA interactions.

4958-66-1

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4958-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4958-66-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,5 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4958-66:
(6*4)+(5*9)+(4*5)+(3*8)+(2*6)+(1*6)=131
131 % 10 = 1
So 4958-66-1 is a valid CAS Registry Number.

4958-66-1SDS

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 (2S)-5-amino-N-(3-amino-3-iminopropyl)-3,4-dihydro-2H-pyrrole-2-carboxamide

1.2 Other means of identification

Product number -
Other names 3',5',N6-triacetyl-2'-deoxyadenosine

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:4958-66-1 SDS

4958-66-1Relevant academic research and scientific papers

Nucleic acid related compounds. 127. Selective N-deacylation of N,O-peracylated nucleosides in superheated methanol

Nowak, Ireneusz,Conda-Sheridan, Martin,Robins, Morris J.

, p. 7455 - 7458 (2007/10/03)

Solutions of peracylated adenosine, cytidine, and related nucleoside derivatives undergo selective N-deacylation upon heating at elevated temperatures (oil bath ≥ 105 °C) in methanol. An increase in the bulk of the N-acyl group has little effect on the rate of N-deacylation but increases the N/O selectivity ratio. Extended heating is required for N-deacylation with arylcarboxylic acid derivatives. Contamination with acidic or basic reagent residues is avoided.

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