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17-methylmorphinan-3-ol 2,3-dihydroxybutanedioate (salt) is a chemical compound derived from the morphine alkaloid, which is found in opium poppy plants. This specific compound is a synthetic opioid that is structurally similar to morphine but has been modified to possess a methyl group at the 17th carbon position. It is known for its potent analgesic properties, which are used to manage severe pain. The 2,3-dihydroxybutanedioate salt form refers to the compound's ionic structure, which can influence its solubility and bioavailability. This chemical is a controlled substance due to its potential for abuse and addiction, and it is used medically under strict regulations to ensure safe and effective pain management.

5497-47-2

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5497-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5497-47-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,9 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5497-47:
(6*5)+(5*4)+(4*9)+(3*7)+(2*4)+(1*7)=122
122 % 10 = 2
So 5497-47-2 is a valid CAS Registry Number.

5497-47-2Downstream Products

5497-47-2Relevant academic research and scientific papers

METHODS FOR PREPARING LEVORPHANOL AND RELATED COMPOUNDS, AND COMPOSITIONS THEREOF

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Paragraph 0177-0182, (2020/04/29)

A method for producing substantially pure levorphanol and related compounds, when compared to the conventional process, is provided. In particular, a method for producing substantially pure levorphanol tartrate dihydrate is described. Also described are compositions comprising levorphanol and related compounds, particularly compositions comprising levorphanol tartrate dihydrate, levomethorphan, and norlevorphanol in which the levomethorphan and norlevorphanol are present in the composition in reduced levels.

PROCESS FOR THE PRODUCTION OF LEVORPHANOL AND RELATED COMPOUNDS

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Page/Page column 5-8, (2008/06/13)

A process for the production of morphinans with higher purity and yield, when compared to the conventional process, is described. Specifically, the process may be used to prepare levorphanol, levorphanol tartrate, and levorphanol tartrate dihydrate in high yields and substantially free from several process impurities.

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