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72739-14-1

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72739-14-1 Usage

Description

S(-)-CATHINONE HYDROCHLORIDE is a psychoactive alkaloid derived from the leaves of the khat plant, Catha edulis Forsk., belonging to the Celastraceae family. It is known for its stimulant properties and is classified as a controlled substance due to its potential for abuse and dependence.

Uses

Used in Pharmaceutical Industry:
S(-)-CATHINONE HYDROCHLORIDE is used as a research chemical for the development of new medications and therapies. Its psychoactive properties make it a valuable compound for studying the effects of stimulants on the central nervous system and their potential applications in treating various medical conditions.
Used in Forensic Science:
S(-)-CATHINONE HYDROCHLORIDE is utilized as a reference substance in forensic science for the identification and analysis of controlled substances in biological samples, such as blood, urine, and hair. This helps in the detection and monitoring of drug abuse and the enforcement of drug control regulations.
Used in Toxicology Research:
S(-)-CATHINONE HYDROCHLORIDE serves as a valuable tool in toxicology research, where it is used to study the toxic effects of stimulants on various organs and systems in the body. This information is crucial for understanding the risks associated with the use of such substances and for developing strategies to mitigate their harmful effects.
Used in Drug Testing and Analysis:
S(-)-CATHINONE HYDROCHLORIDE is employed as a standard for the calibration of analytical instruments and methods used in drug testing and analysis. This ensures the accuracy and reliability of test results, which is essential for the proper enforcement of drug control measures and the protection of public health.

Check Digit Verification of cas no

The CAS Registry Mumber 72739-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,3 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72739-14:
(7*7)+(6*2)+(5*7)+(4*3)+(3*9)+(2*1)+(1*4)=141
141 % 10 = 1
So 72739-14-1 is a valid CAS Registry Number.

72739-14-1SDS

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 (2S)-2-amino-1-phenylpropan-1-one,hydrochloride

1.2 Other means of identification

Product number -
Other names Cathinone 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:72739-14-1 SDS

72739-14-1Relevant articles and documents

A practical synthesis of α-amino ketones via aryllithium addition to N-Boc-α-amino acids

Florjancic, Alan S.,Sheppard, George S.

, p. 1653 - 1656 (2003)

The reaction of N-Boc-α-amino acids with aryllithium reagents followed by removal of the nitrogen protecting group provides enantiomerically pure α-amino aryl ketones as their corresponding HCl salts. This practical two-step sequence gives rapid access to a pharmaceutically interesting class of compounds from commercially available starting materials.

Rearrangement of N-tert-butanesulfinyl α-halo imines with alkoxides to N-tert-butanesulfinyl 2-amino acetals as precursors of N-protected and N-unprotected α-amino carbonyl compounds

Colpaert, Filip,Mangelinckx, Sven,Denolf, Bram,De Kimpe, Norbert

experimental part, p. 6023 - 6032 (2012/10/08)

Reaction of N-tert-butanesulfinyl α-halo imines with alkoxides afforded new N-tert-butanesulfinyl 2-amino acetals in good to excellent yield. These N-tert-butanesulfinyl 2-amino acetals are convenient precursors for the TMSOTf-promoted synthesis of the co

Enantioselective synthesis of both enantiomers of cathinone via the microbiological reduction of 2-azido-1-phenyl-1-propanone

Besse,Veschambre,Dickman,Chenevert

, p. 8288 - 8291 (2007/10/02)

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