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β-methylamino-β-(2-methylphenyl)-ethylamine, also known as 2-(methylamino)-1-(2-methylphenyl)ethanamine, is an organic compound with the chemical formula C10H16N2. It is a derivative of ethylamine, featuring a methyl group attached to the nitrogen atom and a 2-methylphenyl group on the β-carbon. β-methylamino-β-(2-methylphenyl)-ethylamine is a colorless liquid with a pungent odor and is soluble in organic solvents. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Due to its potential applications and reactivity, it is important to handle this chemical with care, adhering to proper safety protocols.

66308-10-9

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66308-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66308-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,0 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66308-10:
(7*6)+(6*6)+(5*3)+(4*0)+(3*8)+(2*1)+(1*0)=119
119 % 10 = 9
So 66308-10-9 is a valid CAS Registry Number.

66308-10-9Relevant academic research and scientific papers

Synthesis and central nervous system properties of 2-[(alkoxycarbonyl)amino]-4(5)-phenyl-2-imidazolines

Weinhardt,Beard,Dvorak,Marx,Patterson,Roszkowski,Schuler,Unger,Wagner,Wallach

, p. 616 - 627 (2007/10/02)

A series of 2-[(alkoxycarbonyl)amino]-4(5)-phenyl-2-imidazolines was prepared and evaluated for central nervous system (CNS) effects (antidepressant, anticonvulsant, muscle relaxant, and depressant) in animal models. Some separation of those CNS activities was achieved through substitutions on the phenyl and imidazoline moieties. Halo-substituted phenyl compounds were among the most potent antidepressants in this series, while imidazole N-alkylation produced compounds with increased depressant effects (loss of righting reflex, mouse behavior). Comparison of in vitro and in vivo data for pairs of 2-[(methoxycarbonyl)amino]-4(5)-phenyl-2-imidazolines and their parent, 2-amino-4(5)-phenyl-2-imidazolines, suggests that the title compounds were prodrugs for the 2-amino-4(5)-phenyl-2-imidazolines in inhibition of norepinephrine reuptake.

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