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2-amino-4-benzylthiopteridine is a chemical compound with the molecular formula C13H12N4S. It is a derivative of pteridine, a heterocyclic organic compound with a pyrimido[4,5-d]pyrimidine core structure. The compound features a benzyl group attached to the 4-position and an amino group at the 2-position, with a sulfur atom incorporated into the ring system. This specific arrangement of functional groups endows 2-amino-4-benzylthiopteridine with unique chemical and biological properties, making it a potential candidate for various applications in pharmaceuticals, agrochemicals, and materials science. Its synthesis and characterization involve advanced organic chemistry techniques, and understanding its reactivity and interactions with other molecules can provide insights into its potential uses and mechanisms of action.

961-26-2

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961-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 961-26-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 961-26:
(5*9)+(4*6)+(3*1)+(2*2)+(1*6)=82
82 % 10 = 2
So 961-26-2 is a valid CAS Registry Number.

961-26-2Downstream Products

961-26-2Relevant academic research and scientific papers

Synthesis of Some Substituted Guanidinopyrimidines and their Structural Assignment by 13C and 1H NMR

Ladd, David L.

, p. 917 - 921 (2007/10/02)

A series of substituted 2- and 4-guanidinopyrimidines were prepared by reaction of halopyrimidines with guanidine; alkylamino and amino substituents were introduced by subsequent halogen replacement by primary amines or ammonia or the catalytic reduction of nitro groups.Structural assignments were made on the basis of 13C and 1H nmr.A guanidinopteridine and a bispyrimidinylguanidine were also synthesized.Some unsuccessful reaction illustrated the low nucleophilic reactivity and thermal instability of the guanidine group.

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