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17α-aza-3α,17α-dihydroxy-D-homo-5α-androstan-17-one 3-acetate is a complex organic compound with the molecular formula C22H33NO4. It is a derivative of the androstane steroid structure, featuring a nitrogen atom at the 17α position, which replaces a carbon atom, hence the term "aza." The compound also has two hydroxyl groups at the 3α and 17α positions, and an acetate group at the 3 position. This molecule is a synthetic analog of natural steroids and is used in medical research for its potential therapeutic applications, particularly in the area of hormone regulation and replacement therapy. Its structure and functional groups give it unique properties that distinguish it from other steroids, making it a subject of interest in the field of medicinal chemistry.

1704-45-6

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1704-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1704-45-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1704-45:
(6*1)+(5*7)+(4*0)+(3*4)+(2*4)+(1*5)=66
66 % 10 = 6
So 1704-45-6 is a valid CAS Registry Number.

1704-45-6Downstream Products

1704-45-6Relevant academic research and scientific papers

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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