3-Furaldehyde

3-Furaldehyde Basic information
Product Name:3-Furaldehyde
Synonyms:BETA-FURFURAL;FURAN-3-CARBALDEHYDE;FURAN-3-CARBOXALDEHYDE;3-Furaldehyde, 97%, stabilized;3-Furaldehyde, Stabilized with ≈:0.05% BHT;3-Formylofuran;3-FURANCARBOXALDEHYDE;3-FURFURAL
CAS:498-60-2
MF:C5H4O2
MW:96.08
EINECS:
Product Categories:Furan&Benzofuran;API intermediates;Aromatic Aldehydes & Derivatives (substituted)
Mol File:498-60-2.mol
3-Furaldehyde Structure
3-Furaldehyde Chemical Properties
Melting point 148-149.5 °C
Boiling point 144 °C/732 mmHg (lit.)
density 1.111 g/mL at 25 °C (lit.)
refractive index n20/D 1.493(lit.)
Fp 119 °F
storage temp. 2-8°C
solubility Chloroform (Soluble), Ethyl Acetate (Slightly)
form Liquid
color Clear yellow to brown
Water Solubility Soluble in water, benzene, chloroform, alcohol and ether.
Sensitive Air & Light Sensitive
BRN 105852
Stability:Light Sensitive
InChIKeyAZVSIHIBYRHSLB-UHFFFAOYSA-N
LogP0.510
CAS DataBase Reference498-60-2(CAS DataBase Reference)
NIST Chemistry Reference3-Furaldehyde(498-60-2)
Safety Information
Hazard Codes Xi,F,T
Risk Statements 10-36/37/38-23/25-21
Safety Statements 26-36-45-36/37-16-3
RIDADR UN 1989 3/PG 3
WGK Germany 3
8-10
Hazard Note Flammable/Harmful
HazardClass 3
PackingGroup III
HS Code 2932190090
MSDS Information
ProviderLanguage
3-Furaldehyde English
SigmaAldrich English
ALFA English
3-Furaldehyde Usage And Synthesis
Chemical PropertiesColorless to light yellow liqui
Uses3-Furaldehyde is a volatile compound of honey of various floral origin. It is used to produce N-furan-3-ylmethylene-N'-pyridin-2-yl-hydrazine by reaction with 2-hydrazino-pyridine. It is also used as a solvent.
DefinitionChEBI: 3-furaldehyde is an aldehyde that is furan substituted by a formyl group at position 3. It has a role as a metabolite. It is a member of furans and an aldehyde. It derives from a hydride of a furan.
Preparationsynthesis of 3-furaldehyde: dissolve 3-furanmethanol (12.0g,0.12mol,1.0eq) in tetrahydrofuran (500ml), add manganese dioxide (156.4g,1.2mol,10.0eq), stir for 18 hours at room temperature, tlc showed that the reaction was completed. the product (9.0g crude) was obtained by filtration and the filtrate was concentrated.
General Description3-Furancarboxaldehyde undergoes photochemical reaction with benzaldehyde to yield oxetane derivatives.
3-Furaldehyde 4-OXO-4,5,6,7-TETRAHYDROBENZO[B]FURAN-3-CARBOXYLIC ACID METHYL 2-METHYL-3-FUROATE COUMESTROL FURFURYL ALCOHOL RESIN 5-HYDROXY-2-METHYL-BENZOFURAN-3-CARBOXYLIC ACID ETHYL ESTER 2-Butyl-3-(4-hydroxybenzoyl)benzofuran 5-METHYLFURAN-3-CARBOXYLIC ACID DIETHYL 3,4-FURANDICARBOXYLATE 3-Furanboronic acid 3-Furoic acid FENFURAM 3-ACETYL-2,5-DIMETHYLFURAN 5-HYDROXY-2-METHYL-BENZOFURAN-3-CARBOXYLIC ACID Furazolidone 3-FURANMETHANOL 2-FURALDEHYDE 99% A.C.S. REAGENT,2-FURALDEHYDE, ACS, STAB.,alpha-furaldehyde[qr METHYL 2,5-DIMETHYL-3-FUROATE

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