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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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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.)
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
95.0 °F - closed cup
Flash Point(C)
35 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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
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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