ChemicalBook--->CAS DataBase List--->88887-87-0

88887-87-0

88887-87-0 Structure

88887-87-0 Structure
IdentificationBack Directory
[Name]

1-Methylcyclopropylamine hydrochloride
[CAS]

88887-87-0
[Synonyms]

1-Methylcyclopropanamine HCl
1-methylcyclopropaneamine HCl
1-Methylcyclopropanaminium chloride
1-Methylcyclopropylamine hydrochloride
1-MethylcyclopropanaMine hydrochloride
1-Methylcyclopropan-1-amine hydrochloride
1-aMino-1-Methylcyclopropane hydrochloride
1-methylcyclopropanamine hydrochloride (1:1)
1-Methylcyclopropan-1-amine hydrochloride 98%
CyclopropanaMine,1-Methyl-, hydrochloride (1:1)
(1-Methylcyclopropyl)aMine hydrochloride (SALTDATA: HCl)
[Molecular Formula]

C4H10ClN
[MDL Number]

MFCD11109576
[MOL File]

88887-87-0.mol
[Molecular Weight]

107.582
Chemical PropertiesBack Directory
[Melting point ]

204-205 °C(Solv: ethyl acetate (141-78-6); methanol (67-56-1))
[storage temp. ]

Inert atmosphere,2-8°C
[Appearance]

Off-white to light brown Solid
[InChI]

InChI=1S/C4H9N.ClH/c1-4(5)2-3-4;/h2-3,5H2,1H3;1H
[InChIKey]

GHILZUOTUJGCDH-UHFFFAOYSA-N
[SMILES]

NC1(C)CC1.[H]Cl
[EPA Substance Registry System]

Cyclopropanamine, 1-methyl-, hydrochloride (1:1) (88887-87-0)
Questions And AnswerBack Directory
[Uses]

1-Methylcyclopropylamine hydrochloride is an amine derivative and can be used as a pharmaceutical intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)Health Hazard (GHS08)
GHS06,GHS08
[Signal word ]

Danger
[Hazard statements ]

H301-H315-H319-H317-H334
[Precautionary statements ]

P501-P261-P272-P270-P264-P280-P284-P302+P352-P342+P311-P337+P313-P305+P351+P338-P362+P364-P304+P340-P333+P313-P301+P310+P330-P405
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

1-Methylcyclopropylamine hydrochloride(88887-87-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Carbamic acid, (1-methylcyclopropyl)-, 1,1-dimethylethyl ester (9CI)

251661-01-5

1-Methylcyclopropylamine hydrochloride

88887-87-0

(2) N-Boc-1-methylcyclopropylamine (4.66 g) obtained in step (1) was dissolved in 1,4-dioxane (10 mL), followed by addition of a 4N hydrochloric acid solution of dioxane (10 mL). The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, diisopropyl ether was added to the mixture and the precipitated crystals were collected by filtration to afford 1-methylcyclopropanamine hydrochloride (2.69 g, yield: 92%) as a colorless solid. Mass spectrum (APCI) m/z: 72 [M+H]+.

[References]

[1] Patent: WO2008/4698, 2008, A2. Location in patent: Page/Page column 129
[2] Patent: WO2011/6074, 2011, A1. Location in patent: Page/Page column 127
[3] Patent: WO2006/67444, 2006, A1. Location in patent: Page/Page column 84-85
[4] Patent: WO2005/42502, 2005, A1. Location in patent: Page/Page column 81-82
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