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1-(2-methylbenzyl)cyclopropanamine(SALTDATA: HCl) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91245-68-0

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91245-68-0 Usage

Chemical compound

A chemical compound commonly used as a pharmaceutical intermediate for the synthesis of various drugs.

Combination with hydrochloric acid

Forms a hydrochloride salt (1-(2-methylbenzyl)cyclopropanamine hydrochloride) that is frequently used in medicinal products.

Potential therapeutic applications

Has been found to have potential for treating various medical conditions, including depression and anxiety.

Pharmacological effects

Exhibits a variety of pharmacological effects, making it a valuable component in the development of new drugs.

Importance in the pharmaceutical industry

1-(2-methylbenzyl)cyclopropanamine hydrochloride is an important chemical in the pharmaceutical industry due to its potential therapeutic applications and pharmacological effects.

Check Digit Verification of cas no

The CAS Registry Mumber 91245-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,4 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91245-68:
(7*9)+(6*1)+(5*2)+(4*4)+(3*5)+(2*6)+(1*8)=130
130 % 10 = 0
So 91245-68-0 is a valid CAS Registry Number.

91245-68-0Downstream Products

91245-68-0Relevant 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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