N-Methyl-1-amino-hex-5-ene

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Products Intro: Product Name:N-Methyl-5-hexen-1-amine
CAS:55863-02-0
Purity:99% Package:50kg;2.2USD|10kg;6.6USD|1kg;8.8USD
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Products Intro: Product Name:N-Methyl-1-amino-hex-5-ene
CAS:55863-02-0
Purity:98% Package:5KG;1KG
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CAS:55863-02-0
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Products Intro: Product Name:N-Methyl-1-amino-hex-5-ene
CAS:55863-02-0
Purity:99% Package:1KG;1USD
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Products Intro: Product Name:5-Hexen-1-amine, N-methyl-
CAS:55863-02-0

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N-Methyl-1-amino-hex-5-ene Basic information
Product Name:N-Methyl-1-amino-hex-5-ene
Synonyms:5-HEXEN-1-AMINE, N-METHYL-;N-methylhex-5-en-1-amine;5-Hexen-1-aMine, N-Methyl-N-Methylhex-5-en-1-aMine;N-methyl-5-hexen-1-amine;N-Methyl-1-amino-hex-5-ene;N-Methylhex-5-en-1-amine,98% (stabilized with MEHQ)
CAS:55863-02-0
MF:C7H15N
MW:113.2
EINECS:
Product Categories:
Mol File:55863-02-0.mol
N-Methyl-1-amino-hex-5-ene Structure
N-Methyl-1-amino-hex-5-ene Chemical Properties
Boiling point 146.5±19.0 °C(Predicted)
density 0.764±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
pka10.74±0.10(Predicted)
form Oil
color Colourless
Stability:Volatile
InChIInChI=1S/C7H15N/c1-3-4-5-6-7-8-2/h3,8H,1,4-7H2,2H3
InChIKeyKKIMETYRXLWWSD-UHFFFAOYSA-N
SMILESC(NC)CCCC=C
Safety Information
MSDS Information
N-Methyl-1-amino-hex-5-ene Usage And Synthesis
UsesN-Methylhex-5-en-1-amine can be used as a reagent to prepare quinazoline substituted cyclopentane and proline-urea based macrocycles as Hepatitis C virus (HCV) NS3/4A protease inhibitors.
Synthesis
6-Bromo-1-hexene

2695-47-8

Methylamine

74-89-5

N-Methyl-1-amino-hex-5-ene

55863-02-0

The following step: To a reaction flask was added a methanol solution containing 25% methylamine in an amount of 10 equivalents of methylamine. Subsequently 1 equivalent of 6-bromo-1-hexene was added to the reaction flask and mixed with stirring. The reaction mixture was heated to 40°C in an oil bath and kept at this temperature for 3 hours. Upon completion of the reaction, the mixture was cooled to 20 °C and 0.1 equivalent of p-methoxyphenol was added as a stabilizer, along with 1 equivalent of sodium hydroxide. The excess methylamine methanol solution was recovered under negative pressure. Next, the mixture was heated to 50 °C and a colorless liquid product, N-methyl-5-hexen-1-amine, was obtained by distillation under reduced pressure. The yield of this step was 67% and the purity of the product was 96.5%.

References[1] Patent: CN108003037, 2018, A. Location in patent: Paragraph 0014-0028
[2] Bulletin de la Societe Chimique de France, 1975, p. 2315 - 2320
N-Methyl-1-amino-hex-5-ene Preparation Products And Raw materials
Raw materialsAcetamide, 2,2,2-trifluoro-N-5-hexen-1-yl-N-methyl--->Methylamine-->6-Bromo-1-hexene
Tag:N-Methyl-1-amino-hex-5-ene(55863-02-0) Related Product Information
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