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14019-10-4

14019-10-4

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14019-10-4 Usage

Uses

The enatiomer of (+)-α-Methadol (M225860) and is more effective in binding to opiate receptors. The relative activities of (-)-α-Methadol and (+)-α-Methadol are reversed upon acetylation. A metabolite of (-)-α-Acetylmethadol (A186325).

Check Digit Verification of cas no

The CAS Registry Mumber 14019-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,1 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14019-10:
(7*1)+(6*4)+(5*0)+(4*1)+(3*9)+(2*1)+(1*0)=64
64 % 10 = 4
So 14019-10-4 is a valid CAS Registry Number.

14019-10-4SDS

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 (-)-α-Methadol

1.2 Other means of identification

Product number -
Other names (3S,6S)-6-(dimethylamino)-4,4-diphenylheptan-3-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:14019-10-4 SDS

14019-10-4Relevant articles and documents

Synthesis of optically active methadones, LAAM and bufuralol by lipase-catalysed acylations

Hull, Jonathan D.,Scheinmann, Feodor,Turner, Nicholas J.

, p. 567 - 576 (2007/10/03)

(R)- and (S)-Methadones and levo-α-acetylmethadol (LAAM) have been synthesised starting from lipase-catalysed acylation of dimethylaminopropan-2-ol. An approach to the synthesis of (R)-bufuralol is also presented.

Synthesis of a new metabolite of acetylmethadol

Booher,Pohland

, p. 266 - 268 (2007/10/06)

The primary amine metabolites of α (±) and α (-) acetylmethadol were synthesized. A neutral permanganate oxidation of noracetylmethadol gave a nitroalkane. This unusual oxidation product was readily converted to the primary amine metabolite of acetylmetha