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6-(3,4-dimethoxyphenyl)hex-1-en-3-one is an organic compound with the molecular formula C14H18O3. It is a derivative of hexenone, featuring a hexenone core structure with a 3,4-dimethoxyphenyl group attached at the 6th position. 6-(3,4-dimethoxyphenyl)hex-1-en-3-one is characterized by its alkenone and aromatic ring systems, which contribute to its chemical properties and potential applications. It is synthesized through various chemical reactions and can be used in the pharmaceutical, fragrance, and flavor industries due to its unique chemical structure and reactivity. The compound's properties, such as its solubility, stability, and potential biological activity, make it a subject of interest for researchers in organic chemistry and related fields.

4126-05-0

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4126-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4126-05-0 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, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4126-05:
(6*4)+(5*1)+(4*2)+(3*6)+(2*0)+(1*5)=60
60 % 10 = 0
So 4126-05-0 is a valid CAS Registry Number.

4126-05-0Relevant 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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