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1-Diethylamino-6-(3,4-dimethoxyphenyl)hexan-3-one is a complex organic compound with the molecular formula C17H27NO3. It is a derivative of hexan-3-one, featuring a diethylamino group at the 1-position and a 3,4-dimethoxyphenyl group at the 6-position. 1-diethylamino-6-(3,4-dimethoxyphenyl)hexan-3-one is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. Its structure provides a unique combination of functional groups, which can contribute to its reactivity and biological activity. The presence of the diethylamino group may confer basic properties, while the dimethoxyphenyl group can influence the compound's lipophilicity and electronic properties. This chemical's specific applications and effects are subject to ongoing research and development in the field of medicinal chemistry.

4126-24-3

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4126-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4126-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,2 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4126-24:
(6*4)+(5*1)+(4*2)+(3*6)+(2*2)+(1*4)=63
63 % 10 = 3
So 4126-24-3 is a valid CAS Registry Number.

4126-24-3Relevant academic research and scientific papers

Synthesis of gon-4-enes

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, (2008/06/13)

1. A therapeutic composition having progestational activity comprising as active ingredient a 17-aliphatic carboxylic acid ester of 17α-ethynyl-18-methyl-19-nortestosterone and a pharmaceutical carrier for said compound.

Synthesis of 13-alkyl-gon-4-ones

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, (2008/06/13)

The preparation of 13-methylgon-4-enes and novel 13-polycarbonalkylgon-4-enes by a new total synthesis is described. 13-Alkylgon-4-enes having progestational, anabolic and androgenic activities are prepared by forming a tetracylic gonane structure unsaturated in the 1,3,5(10),9(11) and 14-positions, selectively reducing in the B- and C-rings, and converting the aromatic A-ring compounds so-produced to gon-4-enes by Birch reduction and hydrolysis.

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