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13β-Ethyl-17β-(3-phenylpropionoxy)-gon-4-en-3-one is a complex organic compound with the molecular formula C28H36O3. It is a derivative of the gonane class of steroids, characterized by the presence of an ethyl group at the 13β position and a 3-phenylpropionoxy group at the 17β position. 13β-Ethyl-17β-(3-phenylpropionoxy)-gon-4-en-3-one is structurally related to natural hormones and has potential applications in pharmaceuticals, particularly in the development of contraceptives and other hormone-related medications. Its chemical structure allows for specific interactions with hormone receptors, which can modulate physiological processes in the body. The compound's unique arrangement of functional groups and its steroidal backbone contribute to its biological activity and potential therapeutic uses.

808-89-9

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808-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 808-89-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,0 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 808-89:
(5*8)+(4*0)+(3*8)+(2*8)+(1*9)=89
89 % 10 = 9
So 808-89-9 is a valid CAS Registry Number.

808-89-9Downstream Products

808-89-9Relevant 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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