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Levophacodyl, also known as levophacetoperane, is a stimulant drug that was once used to treat conditions such as narcolepsy and attention deficit hyperactivity disorder (ADHD). It is the levorotatory enantiomer of the racemic mixture phacodyl, which means it is the left-handed molecular form of the compound. Levophacodyl is believed to work by increasing the levels of dopamine and norepinephrine in the brain, which are neurotransmitters associated with wakefulness and attention. However, due to concerns about its potential for abuse and the availability of safer alternatives, levophacodyl is no longer widely used in medical practice. It is important to note that levophacodyl is not the same as levodopa, which is a different drug used in the treatment of Parkinson's disease.

6192-97-8

6192-97-8 Suppliers

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6192-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6192-97-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6192-97:
(6*6)+(5*1)+(4*9)+(3*2)+(2*9)+(1*7)=108
108 % 10 = 8
So 6192-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H21N/c1-9(11-2)8-10-6-4-3-5-7-10/h9-11H,3-8H2,1-2H3/t9-/m0/s1

6192-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-cyclohexyl-N-methylpropan-2-amine

1.2 Other means of identification

Product number -
Other names d-propylhexedrine

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:6192-97-8 SDS

6192-97-8Relevant academic research and scientific papers

An efficient, scalable process for benzphetamine hydrochloride

Pramanik, Chinmoy,Bapat, Kiran,Chaudhari, Ashok,Kulkarni, Mukund G.,Kolla, Rangarao,Sompalli, Srinivasarao,Tripathy, Narendra K.,Gurjar, Mukund K.

, p. 495 - 500 (2014/05/06)

Commercial manufacturing of benzphetamine hydrochloride along with its impurity profiling is disclosed. Deoxygenation of pseudoephedrine is reported with ～100% retention by shielding the amine group as its tert-butyl carbamate, which is very straightforward to eliminate at the end. Four unknown process-related impurities are isolated from the samples of final API and characterized on the basis of their NMR and mass spectral analysis. Structures of the isolated impurities are confirmed by independent syntheses and coinjecting with the isolated one.