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278866

Sigma-Aldrich

3-Furancarboxaldehyde

≥97%

Synonym(s):

3-Furaldehyde

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5 G
¥13,390

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5 G
¥13,390

About This Item

Empirical Formula (Hill Notation):
C5H4O2
CAS Number:
498-60-2
Molecular Weight:
96.08
Beilstein:
105852
MDL number:
MFCD00010424
UNSPSC Code:
12352100
PubChem Substance ID:
24856838
NACRES:
NA.22

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Quality Level

100

Assay

≥97%

form

liquid

refractive index

n20/D 1.493 (lit.)

bp

144 °C/732 mmHg (lit.)

density

1.111 g/mL at 25 °C (lit.)

functional group

aldehyde

storage temp.

2-8°C

SMILES string

O=Cc1ccoc1

InChI

1S/C5H4O2/c6-3-5-1-2-7-4-5/h1-4H

InChI key

AZVSIHIBYRHSLB-UHFFFAOYSA-N

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General description

3-Furancarboxaldehyde undergoes photochemical reaction with benzaldehyde to yield oxetane derivatives[1].

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

118.4 °F - closed cup

Flash Point(C)

48 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

278866-BULK:
278866-100G:
278866-25G:
278866-5G:
278866-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCH3446
MKBP7756V
MKBT6807V
MKBQ9923V
MKBM9666V

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Maurizio D'Auria et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 9(8), 1134-1138 (2010-06-22)
The photochemical reaction of 2-substituted heterocyclic aldehydes with furan gave the corresponding exo oxetane derivatives through the excited triplet state. However, in situ the oxetane derivatives were converted through a metathesis reaction into the corresponding Z,E-butadienyl formate derivatives. On the

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