Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

159573

Sigma-Aldrich

2-Furonitrile

99%

Synonym(s):

2-Cyanofuran

Sign Into View Organizational & Contract Pricing


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

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.

Signal Word

Danger

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service