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R(+)-CATHINONE HYDROCHLORIDE, a psychoactive alkaloid, is derived from the leaves of the khat plant, Catha edulis Forsk., belonging to the Celastraceae family. It is classified as a controlled substance and acts as a stimulant. This crystalline solid is known for its stimulating effects on the central nervous system.

76333-53-4

76333-53-4 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

76333-53-4 Usage

Uses

Used in Pharmaceutical Industry:
R(+)-CATHINONE HYDROCHLORIDE is used as a stimulant for its psychoactive properties, which can potentially influence the central nervous system and provide temporary relief from fatigue or enhance alertness.
Used in Research and Development:
In the field of scientific research, R(+)-CATHINONE HYDROCHLORIDE serves as a valuable compound for studying the effects of psychoactive substances on the human brain and developing new treatments for various neurological disorders.
Used in Controlled Substance Regulation:
As a controlled substance, R(+)-CATHINONE HYDROCHLORIDE is utilized in the development and enforcement of regulations and policies related to the use, distribution, and possession of stimulant drugs to ensure public safety and prevent abuse.

Check Digit Verification of cas no

The CAS Registry Mumber 76333-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,3 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76333-53:
(7*7)+(6*6)+(5*3)+(4*3)+(3*3)+(2*5)+(1*3)=134
134 % 10 = 4
So 76333-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO.ClH/c1-7(10)9(11)8-5-3-2-4-6-8;/h2-7H,10H2,1H3;1H/t7-;/m1./s1

76333-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-amino-1-phenylpropan-1-one,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:76333-53-4 SDS

76333-53-4Downstream Products

76333-53-4Relevant academic research and scientific papers

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

An efficient synthesis of both enantiomers of Cathinone by regioselective reductive ring opening of substituted aziridines

Hwang, Gweon Il,Chung, Jae-Ho,Lee, Won Koo

, p. 12111 - 12116 (2007/10/03)

Both enantiomers of Cathinone were prepared as HCl salts from N-(R)-α-methylbenzylaziridine-2(S)-carboxaldehyde 2c and its enantiomer N-(S)-α-methyl-benzylaziridine-2(R)-carboxaldehyde 3c in high yield. This process makes it possible to prepare other aromatic and heteroaromatic analogs of Cathinone efficiently.