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1-(2-trifluoromethylbenzyl)cyclopropylamine is a chemical compound with the molecular formula C11H12F3N. It is a derivative of cyclopropylamine, featuring a benzyl group substituted with a trifluoromethyl group at the 2-position. 1-(2-trifluoromethylbenzyl)cyclopropylamine is characterized by its unique structure, which combines the properties of a cyclopropane ring with an aromatic benzene ring. The presence of the trifluoromethyl group imparts specific electronic and steric effects, which can influence the compound's reactivity and physical properties. It is an organic molecule that may be of interest in the fields of medicinal chemistry and materials science due to its potential applications in the development of pharmaceuticals or as a building block in the synthesis of more complex molecules.

716-64-3

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716-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 716-64-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 716-64:
(5*7)+(4*1)+(3*6)+(2*6)+(1*4)=73
73 % 10 = 3
So 716-64-3 is a valid CAS Registry Number.

716-64-3Downstream Products

716-64-3Relevant academic research and scientific papers

Substituted cycloalkyl derivatives for the treatment of respiratory diseases

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Page/Page column 19, (2008/06/13)

N-(Phenyl-substituted cycloalkyl or cycloalkylmethyl)-phenylethanolamine derivatives (I) (including benzo-heterocyclic analogs) are new. Also new are cyclopropylamine or cyclopropylmethylamine derivative intermediates (II). Phenylethanolamine derivatives of formula (I) (including optical isomers, enantiomer mixtures and racemates) and their salts, solvates and hydrates are new. n : 0 or 1; m : 1-4; X : direct bond, 2-6C alkenylene, -O-Q-, -NH-Q-, -S-Q- or -Q-; Q : 1-6C alkylene; R 1>H; and R 3>hydroxyalkyl or halo; or R 1> + R 2>OCH 2CONH, CH 2CH 2CONH, CH=CHCONH, NHCH 2CONH, SCH 2CONH, OCONH, SCONH, NHCONH or OCH 2SO 2NH (all optionally substituted (os) by 1 or 2 of alkyl, OH or halo); R 3>, R 4>H, OH, halo, 1-6C alkyl, 1-6C haloalkyl, 1-6C hydroxyalkyl, NH 2 or mono- or dialkylamino; R 5> - R 8>H, OR 9>, halo, 1-6C alkyl, 1-6C haloalkyl, 1-6C hydroxyalkyl, 3-6C cycloalkyl, 3-6C hydroxycycloalkyl, CN, NO 2, COR 9>, COOR 9>, CONR 10>R 11>, NR 10>R 11>, NR 10>COR 9>, NR 10>SO 2R 12>, SR 12>, SOR 12>, SO 2R 12>, SO 2NR 10>R 11> or halo; or two vicinal groups R 6> - R 8> together= 2-6C alkylene, 2-6C alkenylene or O-Q-O (all os by 1 or 2 of alkyl, alkoxy, OH or halo); R 9> - R 11>H, alkyl, aryl or arylalkyl; R 12>alkyl, aryl or arylalkyl; unless specified otherwise alkyl moieties have 1-4C and aryl moieties 6-10C. An independent claim is included for cycloalkylamine or cycloalkylalkylamine derivative intermediates of formula (II) as new compounds, provided that m= 1. [Image] [Image] ACTIVITY : Antiinflammatory; antiasthmatic; antiallergic; virucide; antibacterial; fungicide; protozoacide; anthelmintic; cardiant; dermatological; immunosuppressive; tocolytic; antiarrhythmic; vasotropic; antipruritic. MECHANISM OF ACTION : beta -Mimetic.

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