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3-Benzyloxylmethyl-3H-purin-6-ylamine is a chemical compound with the molecular formula C13H13N5O. 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 benzyloxylmethyl group attached to the 3-position of the purine ring and an amino group at the 6-position. It is known for its potential applications in medicinal chemistry, particularly in the synthesis of purine-based drugs and as a building block for the development of novel therapeutic agents. The compound's structure and properties make it a valuable intermediate in the creation of various biologically active molecules, highlighting its significance in the field of pharmaceutical research and development.

5593-54-4

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5593-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5593-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,9 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5593-54:
(6*5)+(5*5)+(4*9)+(3*3)+(2*5)+(1*4)=114
114 % 10 = 4
So 5593-54-4 is a valid CAS Registry Number.

5593-54-4Downstream Products

5593-54-4Relevant academic research and scientific papers

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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