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9-Propyl-9H-purin-6-amine, also known as 6-aminopurine or Aminopurine, is an organic compound with the chemical formula C5H7N5. It is a derivative of purine, a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring. 9-propyl-9H-purin-6-amine is a white crystalline solid that is soluble in water and slightly soluble in ethanol. 9-Propyl-9H-purin-6-amine is used as an antiviral and anticancer agent, as well as a research tool in molecular biology to study DNA synthesis and repair mechanisms. It is also used in the synthesis of other purine-based compounds and as a reagent in various chemical reactions.

707-98-2

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707-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 707-98-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 707-98:
(5*7)+(4*0)+(3*7)+(2*9)+(1*8)=82
82 % 10 = 2
So 707-98-2 is a valid CAS Registry Number.

707-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-propylpurin-6-amine

1.2 Other means of identification

Product number -
Other names 9-propyl-9H-purin-6-ylamine

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:707-98-2 SDS

707-98-2Relevant academic research and scientific papers

Synthesis by conjugate radical addition of new heterocyclic amino acids with nucleic acid bases in their side chains

Jones,Berthelot,Iley

, p. 2131 - 2132 (2007/10/03)

N-(2-Iodoethyl) and N-(3-iodopropyl)pyrimidines and purines undergo stereoselective conjugate radical addition with an optically active oxazolidinone acceptor to give syn-adducts that can be converted into pyrimidine and purine amino acids.

Heterocyclic Ambident Nucleophiles. III* The Alkylation of Sodium Adenide

Rasmussen, Malcolm,Hope, Janet M.

, p. 525 - 534 (2007/10/02)

The alkylation of sodium adenide in HCONMe2 (30 deg) with various alkylating agents was analysed by 1H n.m.r. spectroscopy.Widely varying N3:N7:N9 alkylation patterns were observed, depending on the alkylating agent.These patterns are interpreted in terms of the electrostatic, thermodynamic and steric factors involved in the different SN2 transition states appropriate to each alkylating agent.Hydrogen bonding association between the 6-amino group and certain carbonyl containing alkylating agents is proposed to explain the enhancedN7-alkylation in some cases.Support for this latter proposal was obtain from a comparison of the adenine alkylation results with the corresponding alkylation patterns of 6-pivaloylamino- and 6-chloro-purine.

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