64271-00-7

Basic information

• Product Name: 1-(5-methyl-2-furyl)propan-1-amine
• Synonyms: 2-Furanmethanamine, α-ethyl-5-methyl-;1-(5-METHYLFURAN-2-YL)PROPAN-1-AMINE-HCL;1-(5-methyl-2-furyl)propan-1-amine;2-Furanmethanamine, a-ethyl-5-methyl-;1-(5-Methylfuran-2-yl)propan-1-aMine;1-(5-Methylfuran-2-yl)propylamine;alpha-Ethyl-5-methyl-2-furanmethanamine
• CAS NO: 64271-00-7
• Molecular Formula: C₈H₁₃NO
• Molecular Weight: 139.19
• EINECS: 604-604-1
• Mol File: 64271-00-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 167℃
• Flash Point: 55℃
• Appearance: /
• Density: 0.978
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: 1-(5-methyl-2-furyl)propan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(5-methyl-2-furyl)propan-1-amine(64271-00-7)
• EPA Substance Registry System: 1-(5-methyl-2-furyl)propan-1-amine(64271-00-7)

Safety Data

• Hazardous Substances Data: 64271-00-7(Hazardous Substances Data)

Usage

General Description

1-(5-methyl-2-furyl)propan-1-amine is a chemical compound with the molecular formula C8H13NO. It is an amine compound that contains a furan ring and a propyl group. 1-(5-methyl-2-furyl)propan-1-amine is commonly used as a pharmaceutical intermediate in the synthesis of various drugs. It is also utilized in the production of agrochemicals and as a precursor in organic synthesis. 1-(5-methyl-2-furyl)propan-1-amine has potential applications in the field of medicinal chemistry and drug discovery due to its structural properties and reactivity. Additionally, it is important to handle this compound with care due to its potential health hazards and should be used in controlled laboratory conditions.

Upstream product

• 133712-93-3 1-(5-methyl-[2]furyl)-propan-1-one oxime 
• 534-22-5 2-methylfuran 
• 10599-69-6 5-methyl-2-propionylfuran 
• 1099823-22-9 5-methyl-2-propionylfuran 
• 620-02-0 5-Methylfurfural 
• 102022-21-9 N-(5-methylfurfurylidene)-N-(diphenylmethyl)amine 
• 60942-20-3 1-(5-methylfuran-2-yl)propan-1-ol 

Downstream Products

• 2364-75-2 emoxypine 
• 478264-01-6 5-methyl-N-[1-(5-methylfuran-2-yl)-propyl]-2-nitrobenzamide 
• 473727-49-0 C₂₁H₂₃N₃O₅ 
• 780760-09-0 (R)-1-(5-methyl-furan-2-yl)-propylamine D-tartarate 
• 1393117-44-6 4-methyl-N-[1-(5-methylfuran-2-yl)propyl]benzenesulfonamide 

Relevant articles and documents

Manganese=Catalyzed Achmatowicz Rearrangement Using Green Oxidant H2O2

Oxidation reactions have been extensively studied in the context of the transformations of biomass=derived furans. However, in contrast to the vast literature on utilizing the stoichiometric oxidants, such as m=CPBA and NBS, catalytic methods for the oxidative furan=recyclizations remain scarcely investigated. Given this, we report a means of manganese=catalyzed oxidations of furan with low loading, achieving the Achmatowicz rearrangement in the presence of hydrogen peroxide as an environmentally benign oxidant under mild conditions with wide functional group compatibility.

PROCESS AND INTERMEDIATES FOR THE SYNTHESIS OF 1,2-SUBSTITUTED 3,4-DIOXO-1-CYCLOBUTENE COMPOUNDS

This application discloses a novel process for the preparation of 1.2 - substituted 3, 4 - dioxo - 1 - cyclobutene compounds of formula (A), which have utility, for example, in the treatment of CXC chemokine -mediated diseases, and intermediates useful in the synthesis thereof.

A new method for preparation of 3-hydroxypyridines from furfurylamines by photooxygenation

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