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Merck
CN

278866

3-Furancarboxaldehyde

≥97%

Synonym(s):

3-Furaldehyde

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About This Item

Empirical Formula (Hill Notation):
C5H4O2
CAS Number:
498-60-2
Molecular Weight:
96.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24856838
MDL number:
MFCD00010424
Beilstein/REAXYS Number:
105852
Assay:
≥97%
Form:
liquid

Key Documents

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InChI

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

SMILES string

O=Cc1ccoc1

InChI key

AZVSIHIBYRHSLB-UHFFFAOYSA-N

assay

≥97%

form

liquid

bp

144 °C/732 mmHg (lit.)

density

1.111 g/mL at 25 °C (lit.)

functional group

aldehyde

storage temp.

2-8°C

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General description

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

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

118.4 °F - closed cup

flash_point_c

48 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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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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