76333-53-4 Usage
Description
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.
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
76333-53-4Relevant articles and documents
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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