1-Cyclopropyl-1-phenylmethanamine hydrochloride

Base Information

• Chemical Name: 1-Cyclopropyl-1-phenylmethanamine hydrochloride
• CAS No.: 39959-72-3
• Molecular Formula: C10H13N.ClH
• Molecular Weight: 183.681
• Hs Code.: 2921499090
• European Community (EC) Number: 966-108-3
• DSSTox Substance ID: DTXSID20484005
• Mol file: 39959-72-3.mol

Synonyms:39959-72-3;1-cyclopropyl-1-phenylmethanamine hydrochloride;cyclopropyl(phenyl)methanamine hydrochloride;1-Cyclopropyl-1-phenylmethylamine hydrochloride;C-Cyclopropyl-C-phenyl-methylamine hydrochloride;Cyclopropyl(phenyl)methanamine HCl;cyclopropyl(phenyl)methanamine;hydrochloride;MFCD08445589;1-Cyclopropyl-1-phenylmethanamine HCl;CYCLOPROPYLPHENYLMETHYLAMINE HYDROCHLORIDE;1-Cyclopropyl-1-phenylmethylamineHydrochloride;(1S)-1-CYCLOPROPYL-1-PHENYLMETHANAMINE HYDROCHLORIDE;DTXSID20484005;QTUNRTDRPMOQNG-UHFFFAOYSA-N;AKOS015891558;ALPHA-CYCLOPROPYLBENZYLAMINE HCL;KS-9812;SB33478;SB37032;SB38962;alpha-Cyclopropylbenzylamine hydrochloride;SY030000;CS-0205451;FT-0660214;EN300-25339;cyclopropyl(phenyl)methanamine hydrogen chloride;F13978;1-Cyclopropyl-1-phenyl-methylamine hydrochloride;cyclopropylphenylmethylamine hydrochloride, AldrichCPR;Z203239488

Chemical Property of 1-Cyclopropyl-1-phenylmethanamine hydrochloride

Chemical Property:

• PSA: 26.02000
• LogP: 3.59870
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 183.0814771
• Heavy Atom Count: 12
• Complexity: 123

Purity/Quality:

97% ^*data from raw suppliers

1-Cyclopropyl-1-phenylmethanamineHCl 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC1C(C2=CC=CC=C2)N.Cl

Technology Process of 1-Cyclopropyl-1-phenylmethanamine hydrochloride

There total 5 articles about 1-Cyclopropyl-1-phenylmethanamine hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

N-(cyclopropylphenylmethyl)formamide → cyclopropyl(phenyl)methaneamine hydrochloride (39959-72-3,844470-80-0)

Guidance literature:

In hydrogenchloride; isopropyl alcohol;

Reference yield:

cyclopropyl(phenyl)methanone oxime (7555-72-8) → cyclopropyl(phenyl)methaneamine hydrochloride (39959-72-3,844470-80-0)

Guidance literature:

With hydrogenchloride; palladium on activated charcoal; Hydrogenation;

DOI:10.1021/ja01563a049

Reference yield:

cyclopropyl(phenyl)methanone oxime (7555-72-8) → N-(cyclopropylmethyl)benzenamine (36178-60-6) + cyclopropyl(phenyl)methaneamine hydrochloride (39959-72-3,844470-80-0)

Guidance literature:

With lithium aluminium tetrahydride; diethyl ether; Hydrogenation_.und anschliessenden Behandeln mit HCl;

DOI:10.1021/ja01563a049

upstream raw materials:

cyclopropyl(phenyl)methanone oxime

cyclopropyl phenyl ketone

Downstream raw materials:

N-[cyclopropyl(phenyl)methyl]-2-(2-oxo-3,3-diphenylpyrrolidin-1-yl)acetamide

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