34825-70-2

Basic information

• Product Name: 1-AMINO-5-HEXENE
• Synonyms: RARECHEM AN KA 1437;1-AMINO-5-HEXENE;Hex-5-en-1-amine
• CAS NO: 34825-70-2
• Molecular Formula: C₆H₁₃N
• Molecular Weight: 99.17
• Mol File: 34825-70-2.mol
• Article Data: 25

Chemical Properties

• Boiling Point: 139.6 °C at 760 mmHg
• Flash Point: 36.8 °C
• Appearance: /
• Density: 0.784 g/cm³
• PKA: 10.60±0.10(Predicted)
• CAS DataBase Reference: 1-AMINO-5-HEXENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-AMINO-5-HEXENE(34825-70-2)
• EPA Substance Registry System: 1-AMINO-5-HEXENE(34825-70-2)

Safety Data

• Hazardous Substances Data: 34825-70-2(Hazardous Substances Data)

Usage

General Description

1-AMINO-5-HEXENE, also known as 1-pentylamine, is a chemical compound that belongs to the group of amines. It is an organic compound with the molecular formula C6H13N and is commonly used as a building block in the synthesis of various pharmaceuticals and other organic compounds. 1-AMINO-5-HEXENE is a clear, colorless liquid with a strong ammonia-like odor and is highly flammable. It is primarily used as a chemical intermediate in the production of pesticides, rubber accelerators, and pharmaceuticals. Additionally, it is used as a corrosion inhibitor in fuel systems, as a lubricant additive, and in the manufacture of fragrances and flavors. Due to its reactivity and potential health hazards, 1-AMINO-5-HEXENE should be handled with care and in accordance with proper safety protocols.

Upstream product

• 5048-19-1 hex-5-enenitrile 
• 821-77-2 5-hexenylazide 
• 52898-33-6 N-(5-hexenyl)phthalimide 
• 821-41-0 5-Hexen-1-ol 
• 64818-36-6 5-hexenyl methanesulfonate 
• 2695-47-8 6-Bromo-1-hexene 
• 786-32-3 pent-4-enyl p-nitrobenzenosulfonate 
• 4048-33-3 6-amino-1-hexanol 
• 1577-22-6 5-hexenoic acid 
• 28487-09-4 hex-5-enamide 
• 102108-47-4 C₁₃H₁₇N 

Downstream Products

• 157099-64-4 N-(hex-5-enyl)hex-5-enamide 
• 1192-29-6 2-ethyl-1-pyrroline 
• 1462-92-6 6-methyl-2,3,4,5-tetrahydro-pyridine 
• 55108-01-5 1-aminohex-trans-4-ene 
• 87156-74-9 1-aminohex-cis-3-ene 
• 109-05-7 2-Methylpiperidin 
• 176171-61-2 Benzyl-hex-5-en-(E)-ylidene-amine 
• 102108-47-4 Hex-5-enyl-[1-phenyl-meth-(E)-ylidene]-amine 
• 113261-23-7 N-(hex-5-en-1-yl)benzamide 
• 54385-22-7 N-(hex-5-enyl)acetamide 
• 81097-32-7 N-hex-5-enyl(4-methylphenyl)sulfonamide 
• 849214-70-6 N^α-Fmoc-N^ε-Boc-lysyl (5-hexenyl)amide 
• 352311-17-2 hex-5-enyl-isopropylidene-amine 
• 884864-65-7 allyl-[2-(5-benzyloxy-2-hex-5-enylcarbamoyl-3-hydroxy-phenyl)-furan-3-ylmethyl]-carbamic acid tert-butyl ester 

Relevant articles and documents

Immobilization of a non-heme diiron complex encapsulated in an ammonium-type ionic liquid layer modified on an Au electrode: Reactivity of the electrode for O2 reduction

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Palladium-Catalyzed Aerobic Oxidative Cyclization of Aliphatic Alkenyl Amides for the Construction of Pyrrolizidine and Indolizidine Derivatives

An efficient palladium-catalyzed aerobic oxidative cyclization has been developed to synthesize a variety of pyrrolizidine and indolizidine derivatives from simple aliphatic alkenyl amides in moderate to good yields. The reaction features the capability of accessing various N-heterocycles and the use of molecular oxygen (1 atm) as the green oxidant.