F20009
Furfurylamine
≥99%
Sinónimos:
2-Aminomethylfuran
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About This Item
Fórmula empírica (notación de Hill):
C5H7NO
Número de CAS:
Peso molecular:
97.12
Beilstein:
1614
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
En este momento no podemos mostrarle ni los precios ni la disponibilidad
Productos recomendados
densidad de vapor
3.35 (vs air)
Nivel de calidad
presión de vapor
4 mmHg ( 20 °C)
Ensayo
≥99%
Formulario
liquid
índice de refracción
n20/D 1.490 (lit.)
bp
145-146 °C (lit.)
mp
−70 °C (lit.)
densidad
1.099 g/mL at 25 °C (lit.)
cadena SMILES
NCc1ccco1
InChI
1S/C5H7NO/c6-4-5-2-1-3-7-5/h1-3H,4,6H2
Clave InChI
DDRPCXLAQZKBJP-UHFFFAOYSA-N
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Aplicación
- Synthesis of renewable furan-based flame retardants: Research describes the synthesis of renewable furan-based phosphate, utilizing furfurylamine, for superior flame retardancy in biodegradable polylactide, showcasing its potential in enhancing material safety (Li et al., 2024).
- Flame retardant for biomass-based fabrics: The development of a molecularly engineered, fully bio-derived phosphorylated furan-based flame retardant, involving furfurylamine, for biomass-based fabrics highlights advancements in fire safety materials (Chen et al., 2024).
- Near-infrared light-responsive composites: Furfurylamine is involved in the development of bio-benzoxazine/bio-urethane copolymers reinforced with graphene, which are NIR light-responsive shape memory composites, contributing to the field of smart materials (Jamnongpak et al., 2024).
- Intelligent fire early-warning fabrics: A multifunctional polylactic acid sensing fabric, using biomass flame retardants including furfurylamine, is developed for intelligent fire early-warning, demonstrating an integration of safety and technology (Jin et al., 2024).
Palabra de señalización
Danger
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Código de clase de almacenamiento
3 - Flammable liquids
Clase de riesgo para el agua (WGK)
WGK 1
Punto de inflamabilidad (°F)
114.8 °F - DIN 51755 Part 1
Punto de inflamabilidad (°C)
46 °C - DIN 51755 Part 1
Equipo de protección personal
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Amine Garci et al.
Acta crystallographica. Section E, Structure reports online, 67(Pt 11), m1592-m1592 (2012-01-06)
The single-crystal X-ray structure analysis of [RuCl(2)(C(12)H(18))(C(5)H(7)NO)] reveals a distorted piano-stool geometry around the Ru(II) atom, with a hexa-methyl-benzene ligand, two chloride ligands and a furfuryl-amine ligand, the latter coordinating through the amine group. In the crystal, a dimeric structure
Esteban Araya-Hermosilla et al.
Polymers, 13(3) (2021-01-27)
Among smart materials, self-healing is one of the most studied properties. A self-healing polymer can repair the cracks that occurred in the structure of the material. Polyketones, which are high-performance thermoplastic polymers, are a suitable material for a self-healing mechanism:
Wei Gao et al.
Ultrasonics sonochemistry, 44, 152-161 (2018-04-24)
The present study has reported an optimized fabrication and application of a novel PVA/TEOS/Schiff base nanofibers membrane as a highly sensitive copper (II) ions in aqueous environment. Here in, for first time, an ultrasound-assisted synthesized symmetric Schiff base has been
Cécile Ouairy et al.
The Journal of organic chemistry, 75(12), 4311-4314 (2010-05-27)
N-Acylation of furfurylamines provided 1, which on double deprotonation with LDA led to the formation of N-acyl-5-aminopenta-2,4-dienals 2 via an isomerization involving opening of the furan ring. The scope and limitations of the procedure were examined by considering the influence
Marine Janvier et al.
ChemSusChem, 10(4), 738-746 (2017-01-04)
A renewable bisepoxide, SYR-EPO, was prepared from syringaresinol, a naturally occurring bisphenol deriving from sinapic acid, by using a chemo-enzymatic synthetic pathway. Estrogenic activity tests revealed no endocrine disruption for syringaresinol. Its glycidylation afforded SYR-EPO with excellent yield and purity.
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