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509-55-7

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509-55-7 Usage

Allopseudocodeine

synthetic opioid and derivative of codeine
Acts as a prodrug to morphine
Primarily used for analgesic properties
Found in over-the-counter medications
Metabolized in the body to produce morphine
Less potent than codeine
Used as an alternative for patients not responding well to codeine or other opioids
Should be used with caution and under healthcare professional guidance
Carries a risk of addiction and dependence

Check Digit Verification of cas no

The CAS Registry Mumber 509-55-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 509-55:
(5*5)+(4*0)+(3*9)+(2*5)+(1*5)=67
67 % 10 = 7
So 509-55-7 is a valid CAS Registry Number.

509-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Pseudocodein

1.2 Other means of identification

Product number -
Other names 4,5α-epoxy-3-methoxy-17-methyl-morphin-6-en-8α-ol

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:509-55-7 SDS

509-55-7Relevant articles and documents

A total synthesis of (±)-codeine by 1,3-dipolar cycloaddition

Erhard, Thomas,Ehrlich, Gunnar,Metz, Peter

, p. 3892 - 3894 (2011/06/24)

Nitrone cycloaddition on a dearomatized bicyclic phenol enabled the facile construction of the correctly configured phenanthrene skeleton of codeine. Further steps yielded allopseudocodeine in a completely diastereoselective manner and finally (±)-codeine by allylic transposition through the hydrolysis of chlorocodides.

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