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(5α,6α)-17-(CyclopropylMethyl)-4,5-epoxy-6-(MethylaMino)-Morphinan-3,14-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102919-85-7

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102919-85-7 Usage

Chemical Properties

Beige Solid

Uses

Opioid receptor antagonist.

Check Digit Verification of cas no

The CAS Registry Mumber 102919-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,9,1 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102919-85:
(8*1)+(7*0)+(6*2)+(5*9)+(4*1)+(3*9)+(2*8)+(1*5)=117
117 % 10 = 7
So 102919-85-7 is a valid CAS Registry Number.

102919-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6α-N-methylnaltrexamine

1.2 Other means of identification

Product number -
Other names (5Alpha,6Alpha)-17-(Cyclopropylmethyl)-4,5-epoxy-6-(methylamino)-morphinan-3,14-diol

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:102919-85-7 SDS

102919-85-7Relevant academic research and scientific papers

NOVEL MORPHINANS USEFUL FOR TREATING MEDICAL DISORDERS

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Paragraph 0078, (2020/10/20)

The present invention related to novel morphinans, compositions comprising the novel morphinans, and their uses as agonists of the kappa opioid receptor.

Preparation of 6-Alpha-Amino N-Substituted Morphinans by Catalytic Hydrogen Transfer

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Page/Page column 14, (2010/12/29)

The present invention provides processes for the stereoselective synthesis of 6-alpha-amino N-substituted morphinans. In particular, the invention provides processes for the reductive amination of 6-keto N-substituted morphinans by catalytic hydrogen transfer.

SYNTHESIS OF METABOLICALLY STABLE AGENTS FOR ALCOHOL AND DRUG ABUSE

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Page/Page column 44, (2010/04/03)

Disclosed herein are compounds of formula (I); as defined herein, or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising the same, and methods of using these compounds for the treatment of substance addiction.

Morphinan derivatives and pharmaceutical use thereof

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, (2008/06/13)

A morphinan derivative or its pharmaceutically acceptable acid addition salt represented with, for example, and an analgesic, diuretic, antitussive and brain cell protector having its derivative or its salt as the active ingredient are described. The compound of the present invention possesses strong analgesic activity, diuretic action and antitussive action as a highly selective κ-opioid agonist, allowing it to be used as a useful analgesic, diuretic and antitussive. On the other hand, the compound of the present invention also possesses remarkable cerebro-neuroprotective activity, thus allowing it be used as a useful cerebro-neuroprotective agents.

Morphinan derivative and its pharmaceutical applications

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, (2008/06/13)

A morphinan derivative or its pharmacologically allowed acid addition salt represented with compound I, an analgesic and diuretic having its derivative or its salt as the active ingredient, and its production process are described. The compound of the present invention possesses strong analgesic activity and diuretic action as a highly selective κ-opioid agonist, allowing it to be used as a useful analgesic and diuretic.

Brain cell protective agent

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, (2008/06/13)

The present invention relates to a novel brain cell protective agent having for its active ingredient a morphinan derivative represented with Compound 1 STR1 or pharmacologically acceptable acid addition salt thereof. The compounds used in the present inv

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