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α-(+/-)-2'-Hydroxy-2,5-dimethyl-9-ethyl-6,7-benzomorphan is a complex organic compound belonging to the morphinan class, which is derived from morphine. This chemical is characterized by its unique molecular structure, featuring a hydroxyl group at the 2' position, two methyl groups at the 2 and 5 positions, and an ethyl group at the 9 position. It is a racemic mixture, meaning it contains both the R and S enantiomers. α-(+/-)-2'-Hydroxy-2,5-dimethyl-9-ethyl-6,7-benzomorphan is known for its potent analgesic properties and is used in the development of pain-relieving medications. Its structure and activity make it a subject of interest in pharmaceutical research, particularly in the context of opioid drugs.

16864-64-5

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16864-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16864-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,6 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16864-64:
(7*1)+(6*6)+(5*8)+(4*6)+(3*4)+(2*6)+(1*4)=135
135 % 10 = 5
So 16864-64-5 is a valid CAS Registry Number.

16864-64-5Upstream product

16864-64-5Downstream Products

16864-64-5Relevant academic research and scientific papers

Synthesis and pharmacological activity of some N alkyl substituted 9α ethyl 2' hydroxy 5 methyl 6,7 benzomorphans

Uwaydah,May,Harris

, p. 1374 - 1377 (2007/10/05)

A series of N-substituted 9α-ethyl-2'-hydroxy-5-methyl-6,7-benzomorphans was synthesized and evaluated for their narcotic analgesic and antagonistic activities. Compounds 2a and 22 were as potent as morphine in the writhing (PPQ) and hot-plate tests, while a number of compounds demonstrated antagonistic activities greater than nalorphine. Generally, the compounds in this series show activities somewhat greater than the comparable compounds in the 5,9α- dimethyl-6,7-benzomorphan series for analgesic effect and similar or slightly less antagonistic potency.

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