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Merck
CN

159573

2-Furonitrile

99%

Synonym(s):

2-Cyanofuran

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About This Item

Empirical Formula (Hill Notation):
C5H3NO
CAS Number:
Molecular Weight:
93.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-537-4
MDL number:
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Product Name

2-Furonitrile, 99%

InChI key

YXDXXGXWFJCXEB-UHFFFAOYSA-N

InChI

1S/C5H3NO/c6-4-5-2-1-3-7-5/h1-3H

SMILES string

N#Cc1ccco1

assay

99%

form

liquid

refractive index

n20/D 1.479 (lit.)

bp

146-148 °C (lit.)

density

1.064 g/mL at 25 °C (lit.)

functional group

nitrile

Quality Level

Application

2-Furonitrile was employed as substrate to investigate the substrate specificity of nitrilase from Rhodococcus rhodochrous Jl cell.

General description

Infrared and Raman spectra of 2-furonitrile has been studied.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

95.0 °F - closed cup

flash_point_c

35 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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C D Mathew et al.
Applied and environmental microbiology, 54(4), 1030-1032 (1988-04-01)
The nitrilase which occurs abundantly in cells of Rhodococcus rhodochrous J1 catalyzes the direct hydrolysis of 3-cyanopyridine to nicotinic acid without forming nicotinamide. By using resting cells, the reaction conditions for nicotinic acid production were optimized. Under the optimum conditions
Vibrational spectra of 2-and 3-furonitrile.
Volka K, et al.
Spectrochimica Acta Part A: Molecular Spectroscopy, 32(2), 397-401 (1976)
Masazumi Tamura et al.
Nature communications, 6, 8580-8580 (2015-10-06)
Multidentate materials formed by simply mixing heterogeneous and homogeneous components are promising for construction of versatile active sites on the surface of heterogeneous compounds, however, to the best of our knowledge, there are no reports on such materials. Self-assembly of

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