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1-(3-Chloro-phenyl)-N1-methyl-ethane-1,2-diamine is an organic compound with the molecular formula C9H12ClN3. It is a derivative of ethane-1,2-diamine, featuring a 3-chlorophenyl group attached to the nitrogen atom at position 1 and a methyl group at the N1 position. 1-(3-Chloro-phenyl)-N1-methyl-ethane-1,2-diamine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the creation of compounds with biological activity. Its chemical structure allows for further functionalization and modification, making it a versatile intermediate in organic synthesis.

96788-20-4

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96788-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96788-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,8 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96788-20:
(7*9)+(6*6)+(5*7)+(4*8)+(3*8)+(2*2)+(1*0)=194
194 % 10 = 4
So 96788-20-4 is a valid CAS Registry Number.

96788-20-4Downstream Products

96788-20-4Relevant 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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