1645-09-6 Usage
General Description
α,α-Dimethyl-m-(trifluoromethyl)phenethylamine is a synthetic chemical compound that belongs to the class of phenethylamines. It is a potent stimulant and psychoactive substance that acts on the central nervous system, producing effects such as increased alertness, energy, and euphoria. α,α-Dimethyl-m-(trifluoromethyl)phenethylamine is structurally similar to amphetamines and is known to have strong psychedelic properties, making it popular among recreational drug users. Due to its potential for abuse and harmful side effects, α,α-Dimethyl-m-(trifluoromethyl)phenethylamine is a controlled substance in many countries and its use is strictly regulated. It is important for individuals to be aware of the risks associated with this chemical and to avoid its recreational use.
Check Digit Verification of cas no
The CAS Registry Mumber 1645-09-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,4 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1645-09:
(6*1)+(5*6)+(4*4)+(3*5)+(2*0)+(1*9)=76
76 % 10 = 6
So 1645-09-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H14F3N/c1-10(2,15)7-8-4-3-5-9(6-8)11(12,13)14/h3-6H,7,15H2,1-2H3
1645-09-6Relevant articles and documents
Use of 5-hydroxy-4H-benzo[1,4]oxazin-3-ones as β2-adrenoceptor agonists
Hoenke, Christoph,Bouyssou, Thierry,Tautermann, Christofer S.,Rudolf, Klaus,Schnapp, Andreas,Konetzki, Ingo
scheme or table, p. 6640 - 6644 (2010/06/12)
Novel β2-agonists with a 5-hydroxy-4H-benzo[1,4]oxazin-3-one moiety as head group are described. Systematic chemical variations at the phenethylamine residue of these compounds lead to the discovery of compound 6m as potent, full agonist of the β2-adrenoceptor with a high β1/β2-selectivity. Molecular modeling revealed an interaction between the carboxylic acid group of 6m and a lysine residue (K305) of the β2-receptor as putative explanation for the high observed selectivity. Further, compound 6m displayed in a guinea pig in vivo model a complete reversal of acetylcholine induced bronchoconstriction which lasted over the complete study time of 5 h.
