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3,4-seco-cholest-5-ene-3,4-dioic acid is a unique organic compound derived from the cholesterol molecule. It is characterized by the removal of the 3,4 double bond and the formation of a 5-ene double bond, resulting in a seco-structure. 3,4-seco-cholest-5-ene-3,4-dioic acid features two carboxylic acid groups at the 3 and 4 positions, which contribute to its acidic properties. The molecule is of interest in the field of organic chemistry and may have potential applications in the synthesis of various steroidal compounds. Its structure and properties make it a subject of study for understanding the transformations and reactions of cholesterol and its derivatives.

434-11-7

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434-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 434-11-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 434-11:
(5*4)+(4*3)+(3*4)+(2*1)+(1*1)=47
47 % 10 = 7
So 434-11-7 is a valid CAS Registry Number.

434-11-7Upstream product

434-11-7Downstream Products

434-11-7Relevant academic research and scientific papers

Superoxide-, tert-Butoxide-, and Hydroxide-Mediated Autoxidation of 3-Oxo-Δ4 Steroids in Aprotic Media

Frimer, Aryeh A.,Gilinsky-Sharon, Pessia,Hameiri, Judith,Aljadeff, Gladis

, p. 2818 - 2819 (2007/10/02)

The course of the base-catalyzed autoxidation of 3-oxo-Δ4 steroids in aprotic media differs sharply both in yield and product distribution from that reported for protic solvents and involves the oxygenation of the kinetic dienolate.

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