92146-66-2

Basic information

• Product Name: 1-(3-methylbenzyl)cyclopropanamine(SALTDATA: HCl)
• Synonyms: 1-(3-methylbenzyl)cyclopropanamine(SALTDATA: HCl);1-(3-methylbenzyl)cyclopropanamine
• CAS NO: 92146-66-2
• Molecular Formula: C₁₁H₁₅N
• Molecular Weight: 161.2435
• Mol File: 92146-66-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(3-methylbenzyl)cyclopropanamine(SALTDATA: HCl)(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-methylbenzyl)cyclopropanamine(SALTDATA: HCl)(92146-66-2)
• EPA Substance Registry System: 1-(3-methylbenzyl)cyclopropanamine(SALTDATA: HCl)(92146-66-2)

Safety Data

• Hazardous Substances Data: 92146-66-2(Hazardous Substances Data)

Usage

General Description

1-(3-methylbenzyl)cyclopropanamine (SALTDATA: HCl) is a chemical compound with the molecular formula C12H17N. It is a cyclopropanamine derivative with a substituted benzyl group. 1-(3-methylbenzyl)cyclopropanamine(SALTDATA: HCl) is most commonly found as a hydrochloride salt, which is a crystalline solid that is soluble in water. The chemical is used as a precursor in the synthesis of various pharmaceuticals and organic compounds, and it also has potential applications in the field of medicinal chemistry. Additionally, it may have biological activities and effects on the central nervous system, although further research is needed to fully understand its pharmacological properties.

Upstream product

• 29765-57-9 1-(3-Methyl-benzyl)-cyclopropanecarbonyl chloride 
• 29805-83-2 1-(3-Methyl-benzyl)-cyclopropanecarboxylic acid ethyl ester 
• 29765-43-3 1-(3-Methyl-benzyl)-cyclopropanecarboxylic acid 

Relevant articles and documents

Substituted cycloalkyl derivatives for the treatment of respiratory diseases

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.