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6-methyl-5,6,7,8-tetrahydroquinazolin-2-amine is a heterocyclic organic compound with the molecular formula C10H14N2. It is a derivative of quinazolin-2-amine, featuring a methyl group at the 6th position and a saturated ring structure. 6-methyl-5,6,7,8-tetrahydroquinazolin-2-amine is of interest in medicinal chemistry due to its potential as a building block for the synthesis of various bioactive molecules, such as pharmaceuticals and agrochemicals. Its structure allows for further functionalization and modification, making it a versatile intermediate in organic synthesis. The compound's properties, such as solubility and reactivity, can be tailored for specific applications, highlighting its importance in the development of new drugs and chemical compounds.

704-62-1

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704-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 704-62-1 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 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 704-62:
(5*7)+(4*0)+(3*4)+(2*6)+(1*2)=61
61 % 10 = 1
So 704-62-1 is a valid CAS Registry Number.

704-62-1Downstream Products

704-62-1Relevant academic research and scientific papers

A One-Pot Synthesis of 2-Aminopyrimidines from Ketones, Arylacetylenes, and Guanidine

Schmidt, Elena Yu.,Tatarinova, Inna V.,Protsuk, Nadezhda I.,Ushakov, Igor A.,Trofimov, Boris A.

, p. 119 - 125 (2017)

The three-component reaction of ketones, arylacetylenes, and guanidine catalyzed by the KOBut/DMSO system leads to 2-aminopyrimidines in up to 80% yield. Depending on structure of the starting ketones, the aromatization of intermediate dihydropyrimidines occurs either with loss of hydrogen molecules or methylbenzenes. The latter process takes place in the ketones, in which one of the substituents is not a methyl group. The reaction conditions are tolerable for dialkyl-, aryl(hetaryl) alkyl-, and cycloalkyl ketones.

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