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2-Cyanotetrahydrofuran

CAS No.
14631-43-7
Chemical Name:
2-Cyanotetrahydrofuran
Synonyms
2-Cyanotetrahydrofuran;tetrahydro-2-Furancarbonitrile;2-Furancarbonitrile, tetrahydro-;2-tetrahydrofuran-2-carbonitrile
CBNumber:
CB92546103
Molecular Formula:
C5H7NO
Molecular Weight:
97.12
MDL Number:
MFCD07787008
MOL File:
14631-43-7.mol
MSDS File:
SDS
Last updated:2026-05-28 05:44:36

2-Cyanotetrahydrofuran Properties

storage temp. Sealed in dry,Store in freezer, under -20°C
Appearance Colorless to light yellow Liquid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301-H311-H331
Precautionary statements  P261-P280-P301+P310-P311

2-Cyanotetrahydrofuran price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 307330 2-Cyanotetrahydrofuran 14631-43-7 250.00mg $56 2026-05-19 Buy
Matrix Scientific 307330 2-Cyanotetrahydrofuran 14631-43-7 1.00g $154 2026-05-19 Buy
Matrix Scientific 307330 2-Cyanotetrahydrofuran 14631-43-7 5.00g $439 2026-05-19 Buy
aablocks AA001DTP Tetrahydrofuran-2-carbonitrile 95% 14631-43-7 100mg $23 2026-05-28 Buy
aablocks AA001DTP Tetrahydrofuran-2-carbonitrile 95% 14631-43-7 250mg $38 2026-05-28 Buy
Product number Packaging Price Buy
307330 250.00mg $56 Buy
307330 1.00g $154 Buy
307330 5.00g $439 Buy
AA001DTP 100mg $23 Buy
AA001DTP 250mg $38 Buy

2-Cyanotetrahydrofuran Chemical Properties, Uses, Production

Synthesis

2-Furamide,tetrahydro-(6CI,7CI)

91470-28-9

2-Cyanotetrahydrofuran

14631-43-7

General procedure for the synthesis of 2-cyanotetrahydrofuran from tetrahydrofuran-2-carboxamide: Preparation of 2-cyanotetrahydrofuran. Trifluoroacetic anhydride (1.55 g, 7.38 mmol) was slowly added to an anhydrous 1,4-dioxane (10 mL) ice-cold solution (0 °C) of tetrahydrofuran-2-carboxamide (0.77 g, 6.71 mmol) and pyridine (1.06 g, 13.42 mmol) at a rate of one drop every 10 seconds. The addition of trifluoroacetic anhydride was monitored to ensure that the internal temperature was below 5 °C and that the addition was completed within 20 min. The reaction mixture was gradually warmed to room temperature and stirred continuously for 3 hours. Upon completion of the reaction, chloroform (100 mL) was added to the mixture and extracted sequentially with water (30 mL) and saturated aqueous sodium chloride solution (20 mL). The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by fast column chromatography (eluent: hexane to 25% ethyl acetate/hexane gradient elution) to afford 2-cyanotetrahydrofuran (0.51 g, 62% yield) as a colorless oil.1H NMR (CDCl3, 300 MHz) δ: 4.70 (1H, m), 3.96 (2H, m), 2.24 (2H, m), 2.08 (2H, m). m).

References

[1] Patent: US2005/187266, 2005, A1
[2] Patent: WO2004/92145, 2004, A1. Location in patent: Page 137

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2-Cyanotetrahydrofuran tetrahydro-2-Furancarbonitrile 2-tetrahydrofuran-2-carbonitrile 2-Furancarbonitrile, tetrahydro- 14631-43-7