2-Furonitrile

Names

[ CAS No. ]:
617-90-3

[ Name ]:
2-Furonitrile

[Synonym ]:
2-furanacarbonitrile
EINECS 210-537-4
2-Furyl cyanide
2-Furonitrile
2-Cyanofuran
2-furancarbonitrile
MFCD00003223
2-furanocarbonitrile

Chemical & Physical Properties

[ Density]:
1.064 g/mL at 25 °C(lit.)

[ Boiling Point ]:
146-148 °C(lit.)

[ Molecular Formula ]:
C₅H₃NO

[ Molecular Weight ]:
93.08340

[ Flash Point ]:
95 °F

[ Exact Mass ]:
93.02150

[ PSA ]:
36.93000

[ LogP ]:
1.15128

[ Index of Refraction ]:
n20/D 1.479(lit.)

[ Storage condition ]:
Flammables area

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H226-H302 + H312 + H332-H318

[ Precautionary Statements ]:
P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R10;R20/21/22

[ Safety Phrases ]:
S26-S36/37/39-S36/37-S16

[ RIDADR ]:
UN 1993 3/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
6.1

[ HS Code ]:
2932190090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2932190090

[ Summary ]:
2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Articles

Self-assembled hybrid metal oxide base catalysts prepared by simply mixing with organic modifiers.

Nat. Commun. 6 , 8580, (2015)

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 ...

Nitrilase-Catalyzed Production of Nicotinic Acid from 3-Cyanopyridine in Rhodococcus rhodochrous J1.

Appl. Environ. Microbiol. 54(4) , 1030-2, (1988)

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, ...

Vibrational spectra of 2-and 3-furonitrile. Volka K, et al.

Spectrochim. Acta A 32(2) , 397-401, (1976)

3-Amino-2-furonitrile
5-nitro-2-furonitrile
5-Bromo-2-furonitrile
5-Amino-2-furonitrile
5-formyl-2-furonitrile
4-Acetyl-2-furonitrile
3-(pyridin-2-yl)-5-(3-(thiophen-2-yl)-1H-pyrazol-5-yl)-1,2,4-oxadiazole
3-(thiophen-2-yl)-5-(3-(thiophen-2-yl)-1H-pyrazol-5-yl)-1,2,4-oxadiazole
3-(4-methoxyphenyl)-5-(3-(thiophen-2-yl)-1H-pyrazol-5-yl)-1,2,4-oxadiazole
3-(3,4-dimethoxyphenyl)-5-(3-(thiophen-2-yl)-1H-pyrazol-5-yl)-1,2,4-oxadiazole
3-(2,3-dimethoxyphenyl)-5-(3-(thiophen-2-yl)-1H-pyrazol-5-yl)-1,2,4-oxadiazole
3-(2,4-dimethoxyphenyl)-5-(3-(thiophen-2-yl)-1H-pyrazol-5-yl)-1,2,4-oxadiazole
3-(4-bromophenyl)-5-[3-(thiophen-2-yl)-1H-pyrazol-5-yl]-1,2,4-oxadiazole
5-[3-(thiophen-2-yl)-1H-pyrazol-5-yl]-3-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole
3-((2-chlorobenzyl)amino)-1-(3-(trifluoromethyl)phenyl)pyrazin-2(1H)-one
3-((4-chlorobenzyl)amino)-1-(3-(trifluoromethyl)phenyl)pyrazin-2(1H)-one

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