3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE

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Products Intro: Product Name:3,3-Diflurocyclobutanamine hydrochloride
CAS:637031-93-7
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Products Intro: Product Name:3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE
CAS:637031-93-7
Purity:99% Package:25kg Remarks:White to Off-White powder
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CAS:637031-93-7
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CAS:637031-93-7
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3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE manufacturers

3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE Basic information
Product Name:3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE
Synonyms:3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE;3,3-Difluorocyclobutanami...;(3,3-Difluorocyclobutyl)aMine Hydrochloride;CyclobutanaMine, 3,3-difluoro-, hydrochloride (1:1);3,3-difluorocyclobutanaMine hcl;3,3-Diflurocyclobutanamine hydrochloride;3,3-Difluorocyclobutaneamine (hydrochloride);3,3-Difluorocyclobutanamine hydrochloride, >=95%
CAS:637031-93-7
MF:C4H8ClF2N
MW:143.56
EINECS:810-267-2
Product Categories:Aliphatics;Amines;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:637031-93-7.mol
3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE Structure
3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE Chemical Properties
Melting point 296 °C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Methanol (Slightly), Water (Slightly)
form Solid
color White to Off-White
InChIInChI=1S/C4H7F2N.ClH/c5-4(6)1-3(7)2-4;/h3H,1-2,7H2;1H
InChIKeyWLXXTHPAORBNIG-UHFFFAOYSA-N
SMILESFC1(CC(N)C1)F.Cl
Safety Information
Hazard Codes Xn
Risk Statements 22
HS Code 2922390090
MSDS Information
3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE Usage And Synthesis
Uses3,3-Difluorocyclobutanamine hydrochloride is used in the preparation of piperazinyl antiviral agents as well as kinase inhibitors.
Uses3-Halo substituted cyclobutanamine used in the preparation of piperazinyl antiviral agents as well as kinase inhibitors.
Synthesis
benzyl 3,3-difluorocyclobutylcarbaMate

939399-53-8

3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE

637031-93-7

Step C: Synthesis of 3,3-difluorocyclobutylamine hydrochloride. A mixture of benzyl (3,3-difluorocyclobutyl)carbamate (1.47 g, 6.1 mmol) and 10% Pd/C (1 g) in methanol (20 mL) was subjected to a hydrogen atmosphere (1 atm) and stirred overnight at room temperature. After completion of the reaction, the mixture was filtered through a diatomaceous earth pad and washed with methanol. Concentrated hydrochloric acid (2 mL) was added to the filtrate, followed by evaporation of the solvent under vacuum to afford the target product 3,3-difluorocyclobutanamine hydrochloride (0.8 g, 85% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 8.60 (m, 3H), 3.64 (m, 1H), 2.89 (m, 4H).

References[1] Patent: WO2012/9678, 2012, A1. Location in patent: Page/Page column 210
[2] Patent: US2013/303524, 2013, A1. Location in patent: Paragraph 0413-0414
Tag:3,3-DIFLUOROCYCLOBUTANAMINE HYDROCHLORIDE(637031-93-7) Related Product Information
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