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6β-Acetoxy-5α-cholestan-3β,5-diol is a steroidal compound characterized by a cholestane skeleton, which is a type of steroid with a cyclohexane ring fused to two cyclopentane rings. This specific molecule features a hydroxyl group at the 3β and 5α positions, indicating the presence of an alcohol group at these locations. Additionally, an acetoxy group is attached at the 6β position, which means an acetate ester is present at this site. The acetoxy group is an acetyl group (-COCH3) attached to an oxygen atom, which is then bonded to the steroid's carbon at position 6. 6β-Acetoxy-5α-cholestan-3β,5-diol is of interest in the field of organic chemistry, particularly in the study of natural products and the synthesis of pharmaceuticals, due to its structural complexity and potential biological activities.

2701-07-7

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2701-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2701-07-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,0 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2701-07:
(6*2)+(5*7)+(4*0)+(3*1)+(2*0)+(1*7)=57
57 % 10 = 7
So 2701-07-7 is a valid CAS Registry Number.

2701-07-7Upstream product

2701-07-7Downstream Products

2701-07-7Relevant academic research and scientific papers

Lewis acid-catalyzed rearrangement of steroidal oxetanes: revision of the course of solvolysis of 3β-tosyloxy-5β-cholestan-5-ol-6-one.

Foster, Richard W.G.,Maples, Brian A.

, p. 2071 - 2074 (1979)

The BF3-catalysed rearrangement of 6β-acetoxy-3α,5-epoxy-5α-cholestane gave the 3α,5β-diol, the 3α,10α-epoxide, and the 2α,5α-epoxide, and the product of solvolysis of 3β-tosyloxy-5β-cholestan-5-ol-6-one was identified as 3α,5-epoxy-A-homo-B-nor-5α-cholestan-4a-one.

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