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N-(9-benzyl-9H-purin-6-yl)benzamide is a chemical compound with the molecular formula C20H16N4O2. It is a derivative of purine, a heterocyclic aromatic organic compound that is a central component of nucleic acids, such as DNA and RNA. This specific compound features a benzyl group attached to the purine ring at the 9-position and a benzamide group connected to the purine at the 6-position. It is known for its potential applications in medicinal chemistry, particularly as a precursor in the synthesis of purine-based drugs that may have therapeutic properties. The compound's structure allows for further functionalization and modification, making it a valuable intermediate in the development of new pharmaceuticals targeting various diseases.

2770-74-3

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2770-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2770-74-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,7 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2770-74:
(6*2)+(5*7)+(4*7)+(3*0)+(2*7)+(1*4)=93
93 % 10 = 3
So 2770-74-3 is a valid CAS Registry Number.

2770-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-benzyl-N6-benzoyl adenin

1.2 Other means of identification

Product number -
Other names N-(9-Anthrylmethylene)-2-naphthyl

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

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More Details:2770-74-3 SDS

2770-74-3Relevant academic research and scientific papers

The Prominent Effect of N6-Acyl Groups on the Reactivity of 9-Substituted Adenines: A New Method for the Chemical Modification of Adenines

Maki, Yoshifumi,Kameyama, Keiji,Suzuki, Mikio,Sako, Magoichi,Hirota, Kosaku

, p. 3601 - 3654 (2007/10/02)

The effect of various N6-substituents on the C(8)-hydrogen exchange of 9-substituted adenines has been estimated.The kinetic data clearly demonstrate that the N6-acyl groups significantly accelerate the C(8)-hydrogen exchange.This fa

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