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634-03-7

634-03-7

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634-03-7 Usage

Chemical Properties

Pale Yellow Oil

Uses

An Amphetamine derivative. Controlled substance (stimulant).

Brand name

Bontril (Mallinckrodt); Bontril (Valeant); Melfiat (Numark);Adipo ii;Amphasub;Anoxine-t;Arcotrol;Di-ap-trol;Dital;Dyrexan-od;Elphemet;Fringanor;Hyrex-105;Obe-del;Obesan-x;Obex la;Obex-la;Obezine;Panrexin-m;Plegline;Pt-1-5;Reducto;Reton;S 7;Sly-ll;Slyn-ll;Sprx 105;Statobex-d;Stodex;Symetra;Trimcaps;Trimstat;Trimtabs;Weighttrol.

World Health Organization (WHO)

Phendimetrazine, a sympathomimetic amine, was introduced in 1961 for use as an anorexic agent. It retains a place in the treatment of obesity. However, since it has been subject to abuse and because dependence can occur, phendimetrazine is controlled under Schedule IV of the 1971 Convention on Psychotropic Substances. (Reference: (UNCPS4) United Nations Convention on Psychotropic Substances (IV), , , 1971)

Check Digit Verification of cas no

The CAS Registry Mumber 634-03-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 634-03:
(5*6)+(4*3)+(3*4)+(2*0)+(1*3)=57
57 % 10 = 7
So 634-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-10-12(14-9-8-13(10)2)11-6-4-3-5-7-11/h3-7,10,12H,8-9H2,1-2H3/t10-,12+/m0/s1

634-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-3,4-Dimethyl-2-phenylmorpholine

1.2 Other means of identification

Product number -
Other names phendimetrazine

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:634-03-7 SDS

634-03-7Relevant articles and documents

Facile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: Scope and application

Zhou, Ling,Tan, Chong Kiat,Zhou, Jing,Yeung, Ying-Yeung

supporting information; experimental part, p. 10245 - 10247 (2010/09/07)

A new one-pot electrophilic aminoalkoxylation reaction using olefin, cyclic ether, amine, and N-bromosuccinimide has been developed. The olefinic substrates and the cyclic ether partners can be flexibly varied to produce a range of amino ether derivatives. This novel protocol has been applied in the facile and efficient synthesis of biologically active morpholine compounds.

2.3.4-Trisubstituted morpholines

Schmauder,Groeger,Foken

, p. 17 - 20 (2007/10/07)

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