71271-62-0 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
1-(6-methylpyridin-2-yl)propan-2-amine is used as a pharmaceutical candidate for its potential therapeutic properties, particularly in the treatment of neurological disorders and psychiatric diseases. Its unique molecular structure allows it to interact with biological targets, offering new avenues for the development of novel therapeutic agents.
Used in Chemical Synthesis:
1-(6-methylpyridin-2-yl)propan-2-amine serves as a building block in the synthesis of other chemical compounds. Its versatile structure makes it a valuable component in the creation of new molecules with specific properties and functions, contributing to the advancement of organic chemistry.
Used in Organic Chemistry Reactions:
As a reagent, 1-(6-methylpyridin-2-yl)propan-2-amine is employed in various organic chemistry reactions. Its amine functionality can participate in a range of chemical transformations, facilitating the synthesis of complex organic molecules and contributing to the broader field of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 71271-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,7 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71271-62:
(7*7)+(6*1)+(5*2)+(4*7)+(3*1)+(2*6)+(1*2)=110
110 % 10 = 0
So 71271-62-0 is a valid CAS Registry Number.
71271-62-0Relevant academic research and scientific papers
Heterocyclic analogs of amphetamine: Thioureas, dithiocarbamates, and negatively substituted amides
Foye,Tovivich
, p. 591 - 595 (2007/10/04)
A series of heterocyclic analogs of amphetamine was synthesized. The heterocycles employed included the 2-furyl, 2-thienyl, 3-methyl-2 thienyl, 3-pyridyl, and 6-methyl-2-pyridyl rings. The aliphatic amine group was converted to the N-methylthiourea, dithiocarbamate, methanesulfonyl, trifluoromethanesulfonyl, and trifluoroacetyl functions since similar conversions of the β-phenethylamine structure had shown blood pressure-lowering effects and some loss of behavioral effects. P-Chlorophenyl and 1-naphthyl analogs were also converted to these derivatives. Behavioral and other biological effects, including antiarthritic, passive cutaneous anaphylactic, and antimicrobial, were observed. The 3-methyl-2-thienyl analog of amphetamine significantly increased papillary muscle contractile force without producing arrhythmias.
