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41135-98-2

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41135-98-2 Usage

Chemical Properties

Pale Yellow Solid

Uses

Oxymorphinone is a major metabolite of Morphine (M652290).

Check Digit Verification of cas no

The CAS Registry Mumber 41135-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,3 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41135-98:
(7*4)+(6*1)+(5*1)+(4*3)+(3*5)+(2*9)+(1*8)=92
92 % 10 = 2
So 41135-98-2 is a valid CAS Registry Number.

41135-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S,4aS,7aR,12bS)-4a,9-dihydroxy-3-methyl-2,4,7a,13-tetrahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7-one

1.2 Other means of identification

Product number -
Other names Oxymorphinone

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:41135-98-2 SDS

41135-98-2Relevant articles and documents

Direct and simple O-demethylation of thebaine to oripavine

Coop, Andrew,Lewis, John W.,Rice, Kenner C.

, p. 6774 - 6774 (1996)

-

PROCESS FOR OBTAINING 3,14-DIACETYLOXYMORPHONE FROM ORIPAVINE

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Page/Page column 20; 21, (2018/01/17)

The present invention relates to a new process for obtaining 3,14-diacetyloxymorphone from oripavine, a process to transform the obtained 3,14-diacetyloxymorphone into a noroxymorphone and a process to transform said noroxymorphone into naloxone, naltrexone, nalbuphine, nalfurafine or nalmefene.

PROCESS FOR IMPROVED OXYMORPHONE SYNTHESIS

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Paragraph 0644-0655; 0703-0717, (2017/02/24)

Processes for preparing oxymorphone are provided. Said processes encompass a step which is a hydrogenation of an 14-hydroxymorphinone salt in the presence of trifluoroacetic acid and/or a glycol.

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