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Morphinan-6-one,7,8-didehydro-4-hydroxy-3-methoxy-17-methyl-, (14a)- (9CI) is a complex organic compound belonging to the morphinan class, which is derived from the opium poppy plant. This specific compound is characterized by its unique molecular structure, featuring a 6-one core, a 7,8-didehydro group, a 4-hydroxy group, a 3-methoxy group, and a 17-methyl group. It is an important intermediate in the synthesis of various opioids, including codeine and hydrocodone, and plays a significant role in the pharmaceutical industry due to its potential therapeutic applications. However, it is essential to handle Morphinan-6-one,7,8-didehydro-4-hydroxy-3-methoxy-17-methyl-, (14a)- (9CI) with caution, as it may have potential addictive properties and side effects.

596-59-8

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596-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 596-59-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 596-59:
(5*5)+(4*9)+(3*6)+(2*5)+(1*9)=98
98 % 10 = 8
So 596-59-8 is a valid CAS Registry Number.

596-59-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-3-methoxy-11-methyl-9,10-dihydro-5H-9,4b-(epiminoethano)phenanthren-6(8aH)-one

1.2 Other means of identification

Product number -
Other names EINECS 209-888-6

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:596-59-8 SDS

596-59-8Relevant academic research and scientific papers

Total Synthesis of (±)-Thebainone A by Intramolecular Nitrone Cycloaddition

Hahn, Christian,Hennig, André,J?ger, Anne,Küttler, Thomas,Metz, Peter,Wang, Yuzhou

, (2020/04/21)

Using an intramolecular nitrone cycloaddition and a Heck cyclization as the crucial transformations, a total synthesis of the racemic morphine alkaloid thebainone A was accomplished in 22 steps commencing with isovanillin.

Improved synthesis of dihydrothebainone and its 14 β-epimer

Davidson,Gregg

, p. 547 - 558 (2007/10/03)

An improved synthesis for the preparation of diastereomerically pure dihydrothebainone (1) from thebaine (3) is reported. A 41% overall yield was realized over three steps via direct transformation of dihydrothebaine-Φ (4) to thebainone-A (6) with 6N HCl.

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