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N,N-dimethyl-9-(3-nitrobenzyl)-9H-purin-6-amine is a complex organic compound with the molecular formula C15H14N6O3. It is a derivative of purine, a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring. This specific compound features a 3-nitrobenzyl group attached to the purine core, which is further substituted with a dimethylamino group at the 9-position. The presence of the nitro group on the benzyl moiety and the dimethylamino group on the purine ring endow this molecule with unique chemical properties and potential applications in medicinal chemistry, particularly in the development of antiviral and anticancer drugs. The compound's structure and functional groups make it a subject of interest for researchers exploring the interactions between purine derivatives and biological targets.

7008-56-2

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7008-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7008-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7008-56:
(6*7)+(5*0)+(4*0)+(3*8)+(2*5)+(1*6)=82
82 % 10 = 2
So 7008-56-2 is a valid CAS Registry Number.

7008-56-2SDS

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 N,N-dimethyl-9-[(3-nitrophenyl)methyl]purin-6-amine

1.2 Other means of identification

Product number -
Other names 9H-Purin-6-amine,N,N-dimethyl-9-((3-nitrophenyl)methyl)

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:7008-56-2 SDS

7008-56-2Relevant academic research and scientific papers

Synthesis and anti-viral activity of 6-amino- and 6-dimethylamino-9-(aminoacylamidobenzyl)purines

Kelley, James L.,Miller, Carl A.,Selway, John W. T.,Schaeffer, Howard J.

, p. 319 - 324 (2007/10/02)

Several aminoacylamido derivatives of 9-benzyladenine and of 9-benzyl-6-dimethylaminopurine were synthesized for evaluation in anti-viral and anti-bacterial screens and in tests for inhibition of protein synthesis.The 9-aminoacylamidobenzyl)purines were s

6-(Alkylamino)-9-benzyl-9H-purines. A New Class of Anticonvulsant Agents

Kelley, James L.,Krochmal, Mark P.,Linn, James A.,McLean, Ed W.,Soroko, Francis E.

, p. 606 - 612 (2007/10/02)

Several 9-alkyl-6-substituted-purines were synthesized and tested for anticonvulsant activity against maximal electroshock-induced seizures (MES) in rats.Most compounds were prepared in three steps from 5-amino-4,6-dichloropyrimidine or in two steps via alkylation of 6-chloropurine.Potent anticonvulsant activity against MES resided in compounds that contain a benzyl substituent at the 9-position of 6-(methylamino)- or 6-(dimethylamino)purine.Among commonly used agents for control of seizures, this type of structure represents a new class of potent anticonvulsant agents.

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