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(+/-)-1,1,1-trifluoro-3-phenyl-2-aminopropane hydrochloride, also known as 3-F-2-aminopropane hydrochloride, is a psychoactive drug that acts as a stimulant and anorectic. It is a derivative of amphetamine and is commonly referred to as an analogue of phentermine. (+/-)-1,1,1-trifluoro-3-phenyl-2-aminopropane hydrochloride is characterized by its chemical structure, which includes a trifluoromethyl group, a phenyl ring, and an amine group, all of which contribute to its biological activity.

330-70-1

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330-70-1 Usage

Uses

Used in Pharmaceutical Industry:
(+/-)-1,1,1-trifluoro-3-phenyl-2-aminopropane hydrochloride is used as a performance-enhancing drug for its stimulant and anorectic properties. It is often found in dietary supplements and weight loss products, helping individuals to increase energy levels and suppress appetite, thus aiding in weight management.
Used in Research:
(+/-)-1,1,1-trifluoro-3-phenyl-2-aminopropane hydrochloride is used as a research chemical to study its effects on the central nervous system and metabolism. This helps scientists to better understand its mechanisms of action and potential applications in the development of new medications.

Check Digit Verification of cas no

The CAS Registry Mumber 330-70-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 330-70:
(5*3)+(4*3)+(3*0)+(2*7)+(1*0)=41
41 % 10 = 1
So 330-70-1 is a valid CAS Registry Number.

330-70-1Relevant academic research and scientific papers

Reusable Nickel Nanoparticles-Catalyzed Reductive Amination for Selective Synthesis of Primary Amines

Murugesan, Kathiravan,Beller, Matthias,Jagadeesh, Rajenahally V.

supporting information, p. 5064 - 5068 (2019/03/19)

The preparation of nickel nanoparticles as efficient reductive amination catalysts by pyrolysis of in situ generated Ni-tartaric acid complex on silica is presented. The resulting stable and reusable Ni-nanocatalyst enables the synthesis of functionalized and structurally diverse primary benzylic, heterocyclic and aliphatic amines starting from inexpensive and readily available carbonyl compounds and ammonia in presence of molecular hydrogen. Applying this Ni-based amination protocol, -NH2 moiety can be introduced in structurally complex compounds, for example, steroid derivatives and pharmaceuticals.

Biomimetic reductive amination of fluoro aldehydes and ketones via [1,3]-proton shift reaction. Scope and limitations

Ono, Taizo,Kukhar, Valery P.,Soloshonok, Vadim A.

, p. 6563 - 6569 (2007/10/03)

A systematic study of azomethine-azomethine isomerizations of the N-benzylimines 2, derived from fluorinated aldehydes or ketones and benzylamine, has been made. The results reveal that, in sharp contrast to hydrocarbon analogs, fluorinated imines of 2 in triethylamine solution undergo isomerizations to give the corresponding N-benzylidene derivatives 5 (for 5/2 K > 32) in good isolated yields. The rates of the isomerizations depend on the starting imine structures and increase in the following order: aryl perfluoroalkyl ketimine 2m, per(poly)fluoroalkyl aldimine 2a,d-g, perfluoroaryl aldimine 2h, alkyl perfluoroalkyl ketimine 2i,j. The presence of chlorine or bromine atoms in the α-position to the C=N double bond of the starting imine favors a dehydrohalogenation reaction, giving rise to unsaturated products 6-9. The azomethine-azomethine isomerization was studied and proven to proceed essentially (>98%) intramolecularly with isotope exchange experiments. High chemical yields, the simplicity of the experimental procedure, and the low cost of all reagents employed make this biomimetic transamination of fluorocarbonyl compounds a practical method for preparing fluorine-containing amines of biological interest.

A practical route to fluoroalkyl- and fluoroarylamines by base-catalyzed [1,3]-proton shift reaction

Soloshonok,Soloshonok, Vadim A.,Kirilenko,Kirilenko, Alexander G.,Kukhar,Kukhar, Valery P.,Resnati,Resnati, Giuseppe

, p. 3119 - 3122 (2007/10/02)

The base-catalyzed [1,3]-proton shift reaction is shown to be an efficient general approach to fluoroalkyl and fluoroaryl amines starting from appropriate carbonyl compounds and benzylamine.

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