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14648-14-7

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14648-14-7 Usage

Uses

A metabolite of Codeine. Morphine derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 14648-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,4 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14648-14:
(7*1)+(6*4)+(5*6)+(4*4)+(3*8)+(2*1)+(1*4)=107
107 % 10 = 7
So 14648-14-7 is a valid CAS Registry Number.

14648-14-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Norcodeine Hydrochloride

1.2 Other means of identification

Product number -
Other names (4R,4aR,7S,7aR,12bS)-9-methoxy-1,2,3,4,4a,7,7a,13-octahydro-4,12-methanobenzofuro[3,2-e]isoquinoline-7-ol,hydrochloride

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:14648-14-7 SDS

14648-14-7Upstream product

14648-14-7Downstream Products

14648-14-7Relevant articles and documents

Efficient iron-catalyzed n-demethylation of tertiary amine-N-oxides under oxidative conditions

Kok, Gaik B.,Scammells, Peter J.

experimental part, p. 1515 - 1521 (2012/02/04)

An investigation into the influence of oxidative conditions on the efficiency of opiate N-demethylation using iron powder has been carried out under non-classical Polonovski conditions. This approach involves a two-step process of N-oxidation and subsequent treatment of the intermediate N-oxide hydrochloride with the redox catalyst. Significant improvements in rate and yield have been realized for these reactions in the presence of molecular oxygen. In this context, further rate enhancement was achieved by the judicious addition of small amounts of ferric ions, leading to a concomitant reduction in the amount of the zero-valent iron primary catalyst that is required. This has led to a generalized improved methodology for the N-demethylation of oripavine, codeine, morphine, and thebaine. This protocol can also be carried out in one-pot without the need to isolate the intermediate N-oxide.