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16α-allyl-3-(benzyloxy)estra-1,3,5(10)-trien-17β-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106139-63-3

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106139-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106139-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,3 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106139-63:
(8*1)+(7*0)+(6*6)+(5*1)+(4*3)+(3*9)+(2*6)+(1*3)=103
103 % 10 = 3
So 106139-63-3 is a valid CAS Registry Number.

106139-63-3Relevant academic research and scientific papers

Estradiol-16alpha-carboxylic acid esters as locally active estrogens

-

, (2008/06/13)

The present invention relates to analogs of estradiol, which, in their most preferred embodiment, act as locally active estrogens without significant systemic action. A series of 16α-carboxylic acid substituted steroids and their esters is presented which

Estradiol-16alpha-carboxylic acid esters as locally active estrogens.

Labaree,Reynolds,Hochberg

, p. 1802 - 1814 (2007/10/03)

We attempted to design analogues of estradiol to act as locally active estrogens without significant systemic action. We synthesized a series of 16alpha-carboxylic acid substituted steroids and their esters and tested their action in several assays of est

A Short, Stereoselective Route to 16α-(Substituted-alkyl)estradiol Derivatives

Fevig, Thomas L.,Katzenellenbogen, John A.

, p. 247 - 251 (2007/10/02)

A variety of 16α-substituted 17β-estradiol derivatives can be prepared by a convenient two-step procedure: The lithium enolate of estrone 3-O-benzyl or 3-O-tert-butyldimethylsilyl ether undergoes clean, stereospecific alkylation with a variety of allylic,

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