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3β-Acetoxy-5-oxo-5,7-seco-B-nor-cholestan-7-oic acid is a complex organic compound derived from the cholesterol family, characterized by a unique molecular structure. It features a 5,7-seco-B-nor-cholestan core, which means that the molecule has undergone a ring-opening reaction, resulting in a loss of the typical steroidal ring structure. The compound also contains a 3β-acetoxy group, indicating the presence of an acetate ester at the 3β position, and a 5-oxo group, which signifies a carbonyl group at the 5 position. This carbonyl group, along with the seco structure, contributes to the molecule's reactivity and potential applications in chemical research and pharmaceutical development. The compound's name reflects its structural features, providing a clear indication of its chemical composition and properties.

3949-51-7

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3949-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3949-51-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3949-51:
(6*3)+(5*9)+(4*4)+(3*9)+(2*5)+(1*1)=117
117 % 10 = 7
So 3949-51-7 is a valid CAS Registry Number.

3949-51-7Relevant academic research and scientific papers

INTRAMOLECULAR CYCLIZATION OF STEROIDAL DIKETO ALDEHYDES TO ACETALS

Boncza-Tomaszewski, Zbigniew,Duddeck, Helmuth

, p. 925 - 935 (2007/10/02)

As an attempt to prepare diketo aldehydes I and II conjugated ketones III and IV were converted to the respective keto diols V and VI, which were treated with periodic acid and independently with lead tetraacetate.However, instead of desired diketo aldehy

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