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3-Oxo-cyclopentanecarbonitrile

Product Name
3-Oxo-cyclopentanecarbonitrile
CAS No.
41171-91-9
Chemical Name
3-Oxo-cyclopentanecarbonitrile
Synonyms
3-Cyanocyclopentanone;3-Oxo-cyclopentanecarbonitrile;Cyclopentanecarbonitrile, 3-oxo-;3-Oxocyclopentane-1-Carbonitrile
CBNumber
CB12669729
Molecular Formula
C6H7NO
Formula Weight
109.13
MOL File
41171-91-9.mol
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3-Oxo-cyclopentanecarbonitrile Property

Boiling point:
250-270 °C(Press: 1 Torr)
Density 
1.08±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
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Safety

HS Code 
2926907090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

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

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
C988418
Product name
3-Cyanocyclopentanone
Packaging
1g
Price
$720
Updated
2021/12/16
AK Scientific
Product number
5264AQ
Product name
3-Oxocyclopentane-1-Carbonitrile
Packaging
25g
Price
$3716
Updated
2021/12/16
Crysdot
Product number
CD13013554
Product name
3-OXOCYCLOPENTANE-1-CARBONITRILE
Purity
95+%
Packaging
5g
Price
$798
Updated
2021/12/16
Chemenu
Product number
CM320017
Product name
3-oxocyclopentane-1-carbonitrile
Purity
95%
Packaging
5g
Price
$888
Updated
2021/12/16
Chemenu
Product number
CM320017
Product name
3-oxocyclopentane-1-carbonitrile
Purity
95%
Packaging
1g
Price
$299
Updated
2021/12/16
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3-Oxo-cyclopentanecarbonitrile Chemical Properties,Usage,Production

Uses

3-Cyanocyclopentanone is used for catalytic enantioselective conjugate addition of cyanide to enones.

Definition

ChEBI: An alicyclic ketone that is cyclopentanone substituted at position 3 by a cyano group.

Synthesis Reference(s)

The Journal of Organic Chemistry, 38, p. 3455, 1973 DOI: 10.1021/jo00960a002

Synthesis

930-30-3

41171-91-9

General procedure for the synthesis of 3-oxocyclopentanecarbonitrile from 2-cyclopentenone: a mixed solution of 2-cyclopentenone (10 g, 122 mmol), potassium cyanide (9.5 g, 146 mmol), and triethylamine hydrochloride (25 g, 83 mmol) in methanol (150 mL) was stirred for 4 hours at room temperature. Upon completion of the reaction, the reaction mixture was concentrated; the residue was redissolved in ethyl acetate. The resulting solution was washed sequentially with water and saturated saline, dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography (petroleum ether: ethyl acetate = 5:1) to give 7.5 g of 3-oxocyclopentanecarbonitrile.1H NMR (400 MHz, CDCl3): δ 3.13-3.51 (m, 1H), 2.56-2.63 (m, 1H), 2.16-2.48 (m, 5H).

References

[1] Journal of Organic Chemistry, 1997, vol. 62, # 15, p. 5144 - 5155
[2] Chemical and Pharmaceutical Bulletin, 1985, vol. 33, # 5, p. 2164 - 2167
[3] Patent: WO2013/28670, 2013, A1. Location in patent: Page/Page column 119; 120

3-Oxo-cyclopentanecarbonitrile Preparation Products And Raw materials

Raw materials

Preparation Products

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3-Oxo-cyclopentanecarbonitrile Suppliers

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41171-91-9, 3-Oxo-cyclopentanecarbonitrileRelated Search:


  • 3-Oxo-cyclopentanecarbonitrile
  • 3-Oxocyclopentane-1-Carbonitrile
  • Cyclopentanecarbonitrile, 3-oxo-
  • 3-Cyanocyclopentanone
  • 41171-91-9