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N6-butyl-5H-purine-2,6-diamine, also known as 6-butylguanine, is an organic compound with the molecular formula C10H15N5. It is a derivative of guanine, a purine nucleobase found in DNA and RNA. N~6~-butyl-5H-purine-2,6-diamine features a butyl group attached to the nitrogen at position 6 of the guanine molecule, which can influence its chemical properties and potential applications. It is used in various chemical and pharmaceutical research applications, including the synthesis of nucleosides and nucleotides, as well as in the development of new drugs targeting purine-related metabolic pathways. The compound's structure and properties make it a valuable tool in understanding the role of purines in biological systems and in the design of therapeutic agents.

5437-50-3

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5437-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5437-50-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5437-50:
(6*5)+(5*4)+(4*3)+(3*7)+(2*5)+(1*0)=93
93 % 10 = 3
So 5437-50-3 is a valid CAS Registry Number.

5437-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-N-butyl-7H-purine-2,6-diamine

1.2 Other means of identification

Product number -
Other names 2-amino-6-n-butylaminopurine

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:5437-50-3 SDS

5437-50-3Downstream Products

5437-50-3Relevant academic research and scientific papers

Synthesis and antiviral evaluation of bis(POM) prodrugs of (E)-[4′-phosphono-but-2′-en-1′-yl]purine nucleosides

Pradère, Ugo,Roy, Vincent,Montagu, Aurélien,Sari, Ozkan,Hamada, Manabu,Balzarini, Jan,Snoeck, Robert,Andrei, Graciela,Agrofoglio, Luigi A.

, p. 126 - 133 (2013/01/15)

Seventeen hitherto unknown bis(POM) prodrugs of novel (E)-[4′- phosphono-but-2′-en-1′-yl]purine nucleosides were prepared in a straight approach and at good yields. Those compounds were synthesized by the reaction of purine nucleobases directly with the p

An efficient synthesis of substituted cytosines and purines under focused microwave irradiation

Huang, Ling-Kuen,Cherng, Yen-Chih,Cheng, Yann-Ru,Jang, Jing-Pei,Chao, Yi-Ling,Cherng, Yie-Jia

, p. 5323 - 5327 (2008/02/01)

A rapid nucleophilic displacement reaction of 6-chloropurine, 2-amino-6-chloropurine and 5-bromocytosine with various nucleophiles under focused microwave irradiation is described. Using this method, the desired products were obtained with the yields up to 99% in?a?short reaction time.

Solution-phase synthesis of 2,6,9-trisubstituted purines

Fiorini, Maria T.,Abell, Chris

, p. 1827 - 1830 (2007/10/03)

A simple three-step method for the solution-phase combinatorial synthesis of 2,6,9-trisubstituted purines from 2,6-dichloropurine is described. The synthesis exploits the use of resin capture to remove excess reagent used in the final step.

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