ChemicalBook > CAS DataBase List > 2-Cyanotetrahydrofuran

2-Cyanotetrahydrofuran

Product Name
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
Formula Weight
97.12
MOL File
14631-43-7.mol
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2-Cyanotetrahydrofuran Property

storage temp. 
Sealed in dry,Store in freezer, under -20°C
Appearance
Colorless to light yellow Liquid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H311Toxic in contact with skin

H331Toxic if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P311Call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

TRC
Product number
C987888
Product name
2-Cyanotetrahydrofuran
Packaging
250mg
Price
$140
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0361445
Product name
2-CYANOTETRAHYDROFURAN
Purity
95.00%
Packaging
5MG
Price
$495.95
Updated
2021/12/16
AK Scientific
Product number
7250AA
Product name
Tetrahydrofuran-2-carbonitrile
Packaging
10g
Price
$944
Updated
2021/12/16
Crysdot
Product number
CD11253216
Product name
Tetrahydrofuran-2-carbonitrile
Purity
97%
Packaging
5g
Price
$565
Updated
2021/12/16
Chemenu
Product number
CM127436
Product name
tetrahydrofuran-2-carbonitrile
Purity
97%
Packaging
5g
Price
$748
Updated
2021/12/16
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2-Cyanotetrahydrofuran Chemical Properties,Usage,Production

Synthesis

91470-28-9

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

2-Cyanotetrahydrofuran Preparation Products And Raw materials

Raw materials

Preparation Products

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