ChemicalBook--->CAS DataBase List--->930-30-3

930-30-3

930-30-3 Structure

930-30-3 Structure
IdentificationMore
[Name]

2-Cyclopentenone
[CAS]

930-30-3
[Synonyms]

2-CYCLOPENTEN-1-ONE
2-CYCLOPENTENE-1-ONE
2-CYCLOPENTENONE
CPEO
CYCLOPENT-2-ENONE
2_cyclopenten-1-0ne
2-cyclopenten-1-0ne
2-Cyclopentenone-1
3-Cyclopenten-2-one
Cyclopenten-3-one
Cyclopentenone
cyclopenten-2-one
2-Cyclopentenone, pure, 98%
Cyclopent-2-en-1-one 97%
1-Cyclopenten-3-one
2-Cyclopentenone, 98%, pure
Cyclopent-2-en-3-one
[EINECS(EC#)]

213-213-0
[Molecular Formula]

C5H6O
[MDL Number]

MFCD00001401
[Molecular Weight]

82.1
[MOL File]

930-30-3.mol
Chemical PropertiesBack Directory
[Appearance]

clear yellow liquid
[Boiling point ]

64-65 °C19 mm Hg(lit.)
[density ]

0.98 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.481(lit.)
[Fp ]

108 °F
[storage temp. ]

2-8°C
[solubility ]

soluble in Chloroform, Methanol
[form ]

Liquid
[color ]

Clear yellow
[Specific Gravity]

0.980
[Water Solubility ]

almost insoluble
[Detection Methods]

GC
[BRN ]

1446054
[InChI]

InChI=1S/C5H6O/c6-5-3-1-2-4-5/h1,3H,2,4H2
[InChIKey]

BZKFMUIJRXWWQK-UHFFFAOYSA-N
[SMILES]

C1(=O)CCC=C1
[LogP]

-0.114 (est)
[CAS DataBase Reference]

930-30-3(CAS DataBase Reference)
[NIST Chemistry Reference]

2-Cyclopenten-1-one(930-30-3)
[Storage Precautions]

Store under nitrogen
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

R10:Flammable.
R37:Irritating to the respiratory system.
R36/37/38:Irritating to eyes, respiratory system and skin .
R22:Harmful if swallowed.
[Safety Statements ]

S16:Keep away from sources of ignition-No smoking .
S36:Wear suitable protective clothing .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

UN 1224 3/PG 3
[WGK Germany ]

3
[F ]

8
[Hazard Note ]

Irritant
[HazardClass ]

3
[PackingGroup ]

III
[HS Code ]

29142990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Diethyl ether-->Dichloromethane-->Government regulation-->Aluminum chloride-->Carbon tetrachloride-->Calcium carbonate-->Carbon disulfide-->Cyclopentanone-->Calcium hypochlorite-->2,4,6-Collidine-->Cyclopentene, 4-(methylsulfinyl)-4-(methylthio)--->4-PENTENOYL CHLORIDE-->3-CYCLOPENTEN-1-ONE
[Preparation Products]

2,3-dihydro-1H-cyclopenta[b]naphthalen-1-one-->3-Hydroxy-3-methylcyclopentanamine hydrochloride-->7-METHYL-1-INDANONE-->Carbamic acid, N-?(3-?oxocyclopentyl)?-?, 1,?1-?dimethylethyl ester-->Furfuryl alcohol
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

2-Cyclopenten-1-one(930-30-3).msds
Hazard InformationBack Directory
[Description]

2-Cyclopentenone contains two functional groups, a ketone and an alkene. It is a colourless liquid. 2-cyclopenten-1-one selectively induces the expression of the 70-kDa HSP (HSP70) in human cells through cycloheximide-sensitive activation of heat shock transcription factor 1 (HSF1). It is a natural product found in Perilla frutescens[1].
[Chemical Properties]

clear yellow liquid
[Uses]

2-Cyclopenten-1-one(930-30-3) is a versatile electrophile employed in various addition reactions including conjugate addition of organocopper nucleophiles, Michael reaction with silyl enol ethers and siloxanes. It is also used in Diels-Alder cycloadditions and phosphoniosilylations.
[Definition]

ChEBI: 2-cyclopenten-1-one is an enone that is cyclopentanone having a C=C double bond at position 2. It has a role as a Hsp70 inducer. It is an enone and an alicyclic ketone.
[Preparation]

2-Cyclopentenones can be synthesized in a number of ways. One of the routes involves elimination of α-bromo-cyclopentanone using lithium carbonate and Claisen condensation-decarboxylation-isomerization cascades of unsaturated diesters as shown below.
Synthesis of 2-Cyclopenten-1-one
The acid-catalyzed dehydration of cyclopentanediols affords cyclopentenone.
As a functional group, the synthesis of 2-cyclopentenones is accomplished in a variety of other ways, including the Nazarov cyclization reaction from divinyl ketones, Saegusa–Ito oxidation from cyclopentanones, ring-closing metathesis from the corresponding dienes, oxidation of the corresponding cyclic allylic alcohols, and the Pauson–Khand reaction from alkenes, alkynes, and carbon monoxide.
en.wikipedia.org
[References]

[1] A Rossi, M G Santoro, G Elia. “2-Cyclopenten-1-one, a new inducer of heat shock protein 70 with antiviral activity.” The Journal of Biological Chemistry 271 50 (1996): 32192–6.
Spectrum DetailBack Directory
[Spectrum Detail]

2-Cyclopentenone(930-30-3)MS
2-Cyclopentenone(930-30-3)1HNMR
2-Cyclopentenone(930-30-3)13CNMR
2-Cyclopentenone(930-30-3)IR1
2-Cyclopentenone(930-30-3)IR2
2-Cyclopentenone(930-30-3)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Cyclopentenone, pure, 98%(930-30-3)
[Alfa Aesar]

2-Cyclopenten-1-one, 98%(930-30-3)
[Sigma Aldrich]

930-30-3(sigmaaldrich)
[TCI AMERICA]

2-Cyclopenten-1-one,>96.0%(GC)(930-30-3)
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