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1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride

Basic information Safety Supplier Related

1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride Basic information

Product Name:
1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride
Synonyms:
  • 1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride
  • 1-Aminocyclopropanemethanol hydrochloride
  • (1-Aminocyclopropyl)methanol hydrochloride, 98%
  • CyclopropaneMethanol, 1-aMino- (hydrochloride)(1:1)
  • (1-AMINOCYCLOPROPYL)METHANOL HCL
  • [1-(hydroxymethyl)cyclopropyl]azanium chloride
  • 1-Amino-cyclopropanemethanol·HCL
  • [1-(hydroxymethyl)cyclopropyl]azanium
CAS:
115652-52-3
MF:
C4H9NO.HCl
MW:
123.58
EINECS:
808-869-5
Mol File:
115652-52-3.mol
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1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride Chemical Properties

Melting point:
119 ºC (DEC.)
storage temp. 
Inert atmosphere,Room Temperature
Appearance
White to off-white Solid
InChI
InChI=1S/C4H9NO.ClH/c5-4(3-6)1-2-4;/h6H,1-3,5H2;1H
InChIKey
ULEMJGCUGKDKTD-UHFFFAOYSA-N
SMILES
C1(N)(CO)CC1.[H]Cl
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Safety Information

HS Code 
2922190090
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1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride Usage And Synthesis

Synthesis

107017-73-2

115652-52-3

8.2 Synthesis of 1-aminocyclopropane methanol hydrochloride 1.04 g of tert-butyl (1-hydroxymethylcyclopropyl)-carbamate was dissolved in 5 mL of dioxane. Under stirring, 2.5 mL of 4 mol/L HCl in dioxane solution was added slowly and dropwise. The reaction mixture was stirred at room temperature for 15 hours. Subsequently, the solvent was evaporated to half of the original volume and the precipitated solid was collected by filtration. 0.5 g of the target product 1-aminocyclopropanemethanol hydrochloride was finally obtained. The structure of the product was confirmed by 1H NMR (400 MHz, DMSO): δ 5.27 (1H, t), 0.91 (2H, t), 0.71 (2H, t).

References

[1] Journal of Medicinal Chemistry, 1988, vol. 31, # 10, p. 2004 - 2008
[2] European Journal of Organic Chemistry, 2005, # 11, p. 2250 - 2258
[3] Patent: US2010/305102, 2010, A1. Location in patent: Page/Page column 16
[4] Patent: US2011/21501, 2011, A1. Location in patent: Page/Page column 59
[5] Patent: US2011/28441, 2011, A1. Location in patent: Page/Page column 14

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