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13β-propyl-3-methoxygona-1,3,5(10),8-tetraen-17-one is a complex organic compound with the molecular formula C22H32O2. It is a derivative of the gonane class of steroids, which are naturally occurring organic compounds that play a crucial role in various biological processes, such as hormone regulation and reproduction. This specific compound features a 13β-propyl group, a 3-methoxy group, and a tetraen-17-one structure, which contribute to its unique chemical properties and potential applications in pharmaceuticals and other industries. Due to its complex structure, it is essential to study its synthesis, stability, and interactions with other molecules to fully understand its potential uses and effects.

2627-90-9

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2627-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2627-90-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2627-90:
(6*2)+(5*6)+(4*2)+(3*7)+(2*9)+(1*0)=89
89 % 10 = 9
So 2627-90-9 is a valid CAS Registry Number.

2627-90-9Downstream Products

2627-90-9Relevant 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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