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3-phenoxy-N-methylmorphinan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67562-76-9

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67562-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67562-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67562-76:
(7*6)+(6*7)+(5*5)+(4*6)+(3*2)+(2*7)+(1*6)=159
159 % 10 = 9
So 67562-76-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H27NO/c1-24-14-13-23-12-6-5-9-20(23)22(24)15-17-10-11-19(16-21(17)23)25-18-7-3-2-4-8-18/h2-4,7-8,10-11,16,20,22H,5-6,9,12-15H2,1H3/t20-,22?,23-/m0/s1

67562-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-3-phenoxy-N-methylmorphinan

1.2 Other means of identification

Product number -
Other names 3-phenoxy-N-methylmorphinan

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:67562-76-9 SDS

67562-76-9Relevant academic research and scientific papers

O-aryl ethers of morphinans

-

, (2008/06/13)

The use of a compound of the formula: wherein R2 is aryl, heteroaryl or a group of the formula R20 and R1 is hydrogen, alkyl, a group of the formula -C(Y,Y1)CH2OH or -CH2W, wherein one of Y and Y1 is hydrogen and the other

Potential synthetic codeine substitutes: (-)-3-O-aryl-N-methylmorphinans

Mohacsi,Hayes,Spinwall

, p. 1219 - 1222 (2007/10/02)

A series of novel O-aryl-N-methylmorphinans were synthesized by the Ullmann reaction from levorphanol in our search for a synthetic codeine substitute with reduced addition liability. The compounds were evaluated for antinociceptive potency and receptor b

Process for preparing 3-phenoxy morphinans

-

, (2008/06/13)

The preparation of 3-phenoxy N-substituted morphinans, useful as analgesics from 1-(p-hydroxybenzyl)-1,2,3,4,5,6,7,8-octahydroisoquinoline or cyclohexen-(1)-yl-ethylamine and p-phenoxyphenylacetic acid is described.

3-Phenoxymorphinans and derivatives thereof

-

, (2008/06/13)

Levo-rotary 3-phenoxy N-substituted morphinans and derivatives thereof useful as analgesics and/or narcotic antagonists and their preparation form (-)-3-hydroxy-N-lower alkyl morphinan including intermediates in this preparation.

3-Phenoxymorphinans and derivatives thereof

-

, (2008/06/13)

Levo-rotary 3-phenoxy N-substituted morphinans and derivatives thereof useful as analgesics and/or narcotic antagonists and their preparation form (-)-3-hydroxy-N-lower alkyl morphinan including intermediates in this preparation.

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