86236-77-3 Usage
Uses
Used in Pharmaceutical Research and Development:
1,3-Dibenzyl-5-cyanohexahydropyrimidine is used as a building block in the synthesis of new compounds with potential biological activity. Its unique structure allows for the creation of novel pharmaceutical compounds that can be further studied and developed for various therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 1,3-Dibenzyl-5-cyanohexahydropyrimidine serves as a key intermediate, enabling the formation of a wide range of chemical compounds. Its versatility in reactions makes it a valuable component in the synthesis of various organic compounds for research and industrial applications.
Used in Drug Development:
1,3-Dibenzyl-5-cyanohexahydropyrimidine is used as a precursor in the development of new drugs. Its potential as a building block for biologically active compounds makes it a promising candidate for the creation of innovative pharmaceuticals that can address unmet medical needs.
Used in Laboratory Research:
In a laboratory setting, 1,3-Dibenzyl-5-cyanohexahydropyrimidine is used for research purposes, where its properties and reactivity are studied to gain insights into its potential applications and to develop new synthetic methods. Researchers utilize 1,3-DIBENZYL-5-CYANOHEXAHYDROPYRIMIDINE to explore its interactions with other molecules and to understand its role in various chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 86236-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,3 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86236-77:
(7*8)+(6*6)+(5*2)+(4*3)+(3*6)+(2*7)+(1*7)=153
153 % 10 = 3
So 86236-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H21N3/c20-11-19-14-21(12-17-7-3-1-4-8-17)16-22(15-19)13-18-9-5-2-6-10-18/h1-10,19H,12-16H2
86236-77-3Relevant academic research and scientific papers
Decarboxylation Reaction. X. Introduction of a Carbon unit at the α-Position of Amines by Reaction of Hexahydro-1,3,5-triazines with Carboxylic Acids
Fukawa, Hidemichi,Terao, Yoshiyasu,Achiwa, Kazuo,Sehiya, Minoru
, p. 94 - 99 (2007/10/02)
An efficient method for introducing a carbon unit at the α-position of alicyclic amines is described.The method involves the reaction of monocyclic or tetracyclic hexahydro-1,3,5-triazines with trichloroacetic acid, cyanoacetic acid, malonic acid and their derivatives, which are introduced into the α-position of amines in the decarboxylated form.Keywords --- 1,3,5-trialkylhexahydro-1,3,5-triazine; trimer of alicyclic imine; decarboxylation; β-amino acid; carboxylic acid
