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17β-acetoxy-1α-bromomethylandrost-4-en-3-one is a synthetic steroidal compound characterized by its unique molecular structure. It features a 17β-acetoxy group, which is an acetate ester attached to the 17β position of the steroid nucleus, and a 1α-bromomethyl group, which is a bromine atom attached to a methyl group at the 1α position. The androst-4-en-3-one part of the name indicates the presence of a four-carbon double bond (en) in the A-ring of the steroid and a ketone (one) at the 3 position. 17β-acetoxy-1α-bromomethylandrost-4-en-3-one is often used in the synthesis of other steroids and has potential applications in pharmaceuticals and chemical research due to its structural properties.

5846-47-9

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5846-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5846-47-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5846-47:
(6*5)+(5*8)+(4*4)+(3*6)+(2*4)+(1*7)=119
119 % 10 = 9
So 5846-47-9 is a valid CAS Registry Number.

5846-47-9Relevant academic research and scientific papers

The Reaction of Some 1α,2α- and 2α,3α-Methylene Steroids with Hydrobromic Acid

Hanson, James R.,Knights, Steve G.

, p. 24 - 28 (2007/10/02)

Treatment of 17β-acetoxy-methyleneandrost-4-en-3-one under the conditions of the dienone-phenol rearrangement affords 17β-acetoxy-1α-bromomethylandrost-4-en-3-one rather than a phenol.The corresponding 3α-alcohol gave a 1α-bromothexyl-3,5-diene rather than an aromatic compounds. 2α,3α-methyleneandrost-5-ene-4,17-dione also gave a 2α-bromomethylandrost-5-ene-4,17-dione rather than a phenol.

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