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About This Item
Empirical Formula (Hill Notation):
C5H3NO
CAS Number:
Molecular Weight:
93.08
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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
SMILES string
N#Cc1ccco1
InChI
1S/C5H3NO/c6-4-5-2-1-3-7-5/h1-3H
InChI key
YXDXXGXWFJCXEB-UHFFFAOYSA-N
General description
Infrared and Raman spectra of 2-furonitrile has been studied.
Application
2-Furonitrile was employed as substrate to investigate the substrate specificity of nitrilase from Rhodococcus rhodochrous Jl cell.
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_germany
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
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Vibrational spectra of 2-and 3-furonitrile.
Volka K, et al.
Spectrochimica Acta Part A: Molecular Spectroscopy, 32(2), 397-401 (1976)
Nitrilase-Catalyzed Production of Nicotinic Acid from 3-Cyanopyridine in Rhodococcus rhodochrous J1.
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
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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