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7H-Purine, 6-chloro-7-[(4-nitrophenyl)methyl]-, also known as 6-chloro-7-(4-nitrobenzyl)purine, is a chemical compound belonging to the purine family. It is characterized by a purine ring structure with a chlorine atom at the 6th position and a 4-nitrobenzyl group attached to the 7th position. 7H-Purine, 6-chloro-7-[(4-nitrophenyl)methyl]- is often used in the synthesis of various biologically active molecules, such as nucleosides and nucleotides, which play crucial roles in cellular metabolism and genetic information storage. The 6-chloro-7-(4-nitrobenzyl)purine structure provides a versatile platform for further chemical modifications, making it a valuable intermediate in medicinal chemistry and drug development.

4230-25-5

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4230-25-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4230-25-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4230-25:
(6*4)+(5*2)+(4*3)+(3*0)+(2*2)+(1*5)=55
55 % 10 = 5
So 4230-25-5 is a valid CAS Registry Number.

4230-25-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-7-(4-nitrophenylmethyl)-7H-purine

1.2 Other means of identification

Product number -
Other names 6-Chloro-7-p-nitrobenzylpurine

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:4230-25-5 SDS

4230-25-5Downstream Products

4230-25-5Relevant academic research and scientific papers

Synthesis, biological activity, and SAR of antimycobacterial 9-aryl-, 9-arylsulfonyl-, and 9-benzyl-6-(2-furyl)purines

Bakkestuen, Anne Kristin,Gundersen, Lise-Lotte,Utenova, Bibigul T.

, p. 2710 - 2723 (2007/10/03)

9-Aryl-, 9-arylsulfonyl- and 9-benzyl-6-(2-furyl)purines were synthesized by N-alkylation or N-arylation of the purine followed by Stille coupling to introduce the furyl substituent in the 6-position and the compounds screened for activity against Mycobac

Purine N-alkylated derivatives. SRN1 synthesis and functional group transformations

Gharbaoui, Tawfik,Benhida, Rachid,Chastanet, Jacqueline,Lechevallier, Andre,Maillos, Philippe,Beugelmans, Rene

, p. 561 - 574 (2007/10/02)

Purine and its 6-chloro, 6-methoxy, 6-amino and 2-amino-6-chloro derivatives are efficient nucleophiyles in SRN1 reactions with various functionalized gem halo-nitroalkanes as substrates in which good regioselectivity on N9 is observ

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