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1-Benzyl-1,4,5,6-tetrahydropyrimidine is a heterocyclic organic compound with the molecular formula C11H14N2. It is a derivative of pyrimidine, a six-membered aromatic ring containing four carbon atoms and two nitrogen atoms. The compound features a benzyl group (C6H5-CH2-) attached to the nitrogen atom at position 1, and the remaining carbon atoms are connected in a tetrahedral arrangement, forming a saturated ring structure. 1-benzyl-1,4,5,6-tetrahydropyrimidine is of interest in medicinal chemistry and drug design due to its potential as a building block for various biologically active molecules, such as antiviral and anticancer agents. Its chemical properties and reactivity can be influenced by the presence of the benzyl group, which can participate in various chemical reactions, such as nucleophilic aromatic substitution and electrophilic aromatic substitution.

1602-94-4

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1602-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1602-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1602-94:
(6*1)+(5*6)+(4*0)+(3*2)+(2*9)+(1*4)=64
64 % 10 = 4
So 1602-94-4 is a valid CAS Registry Number.

1602-94-4Relevant academic research and scientific papers

A synthesis and properties of 1-substituted 1,4,5,6-tetrahydropyrimidines

Alici, Bülent,?etinkaya, Engin,?etinkaya, Bekir

, p. 29 - 36 (2007/10/03)

The condensation of 1-substituted 1,3-diaminopropane with N,N-dimethyl-formamide dimethylacetal gives 1-alkyl- or aryl-1,4,5,6-tetrahydropyrimidines (2) and (3). Alkylation of the tetrahydropyrimidine derivatives with alkyl halides produces the 1,3-dialkyltetrahydropyrimidinium salts (4 and 5). The attempted dehydrogenation of 2 with sulfur leads to insertion of sulfur on the molecule.

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