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3β-acetoxycholestan-6β-ol is a steroidal compound characterized by a cholestane skeleton, which is a derivative of cholesterol. This molecule features a hydroxyl group (-OH) at the 6β position and an acetoxy group (-OAc) at the 3β position. The acetoxy group is an acetyl ester of the hydroxyl group, which can be hydrolyzed under basic conditions to regenerate the hydroxyl group. This is compound of interest in the field of organic chemistry and may have applications in pharmaceuticals or as an intermediate in the synthesis of other steroidal compounds. It is important to note that the specific biological activity or pharmacological properties of 3β-acetoxycholestan-6β-ol are not detailed in this summary, as they would require additional context or specific studies to elucidate.

1256-82-2

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1256-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1256-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,5 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1256-82:
(6*1)+(5*2)+(4*5)+(3*6)+(2*8)+(1*2)=72
72 % 10 = 2
So 1256-82-2 is a valid CAS Registry Number.

1256-82-2Downstream Products

1256-82-2Relevant academic research and scientific papers

REACTION OF BROMOHYDRINS WITH CHLOROTRIS(TRIPHENYLPHOSPHINE)COBALT(I)

Momose, Den-ichi,Yamada, Yasuji

, p. 2669 - 2672 (2007/10/02)

Bromohydrins were converted into ketones in high yields by the reaction with chlorotris(triphenylphosphine)cobalt(I) in the presence of amine or olefin.A probable path-way for the formation of ketones from bromohydrins was also described.

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