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3α-acetoxy-5α-androstane 17-oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49566-82-7

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49566-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49566-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,6 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 49566-82:
(7*4)+(6*9)+(5*5)+(4*6)+(3*6)+(2*8)+(1*2)=167
167 % 10 = 7
So 49566-82-7 is a valid CAS Registry Number.

49566-82-7Downstream Products

49566-82-7Relevant academic research and scientific papers

STEROIDS .LIII. TRANSFORMATION OF 3β-ACETOXY-5α-ANDROSTAN-17-ONE INTO 17α- AND 17β-AMINO DERIVATIVES OF 5α-ANDROSTAN-3β-OL

Nadaraia, N. Sh.,Sladkov, V. I.,Kuleshova, L. N.,Suvorov, N. N.

, p. 481 - 485 (2007/10/02)

The epimeric 17α- and 17β-amino-5α-androstan-3β-ols were synthesized from 3β-acetoxy-5α-androstan-17-one.The configurations at the C17 atom were demonstrated by the 1H NMR method.

Novel Intramolecular Photorearrangement of Nitronate Anions

Yamada, Kazutoshi,Tanaka, Seiji,Naruchi, Kiyoshi,Yamamoto, Makoto

, p. 5283 - 5289 (2007/10/02)

The photochemistry of alkanenitronate anions is described.Irradiation of the alkanenitronate anions leads to hydroxamic acids by oxygen photorearrangement via ?-?* triplet excited states.The stoichiometry of reaction, anion structure and selectivity of migration, the nature of the excited state, the quantum yield of reaction, rehybridization on excitation, and the base dependency are discussed.From the results of a detailed structural study of 19 products it was found that this photorearrangement is a highly regio- and stereospecific reaction.

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