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35878-28-5

35878-28-5 Structure

35878-28-5 Structure
IdentificationBack Directory
[Name]

CYCLOPENTANE-1,2-DICARBOXYLIC ACID ANHYDRIDE
[CAS]

35878-28-5
[Synonyms]

cis-cyclopentane-1,2-dicarboxylic anhydride
(1S,5R)-3-Oxabicyclo[3.3.0]octane-2,4-dione
CYCLOPENTANE-1,2-DICARBOXYLIC ACID ANHYDRIDE
cis-Tetrahydro-1H-cyclopenta[c]furan-1,3(3aH)
(1R,2S)-Cyclopentane-1,2-dicarboxylic anhydride
cis-Cyclopentane-1,2-dicarboxylic acid anhydride
cis-tetrahydro-1H-cyclopenta[c]furan-1,3(4H)-dione
cis-tetrahydro-1H-cyclopenta[c]furan-1,3(3aH)-dione
(3aα,6aα)-Hexahydro-1H-cyclopenta[c]furan-1,3-dione
4,5,6,6a-tetrahydro-3aH-cyclopenta[c]furan-1,3-dione
cis-1,2-Cyclopentanedicarboxylic anhydride >=97.0% (GC)
3aα,5,6,6aα-Tetrahydro-1H-cyclopenta[c]furan-1,3(4H)-dione
1H-Cyclopenta[c]furan-1,3(3aH)-dione,tetrahydro-, (3aR,6aS)-rel-
[EINECS(EC#)]

252-773-0
[Molecular Formula]

C7H8O3
[MDL Number]

MFCD08060139
[MOL File]

35878-28-5.mol
[Molecular Weight]

140.14
Chemical PropertiesBack Directory
[Melting point ]

73-74 °C
[Boiling point ]

84-86°C/0.5mm
[density ]

1.309±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[Appearance]

White to off-white Solid
[BRN ]

12396898
[InChI]

InChI=1/C7H8O3/c8-6-4-2-1-3-5(4)7(9)10-6/h4-5H,1-3H2/t4-,5+
[InChIKey]

NMSRALOLNIBERV-SYDPRGILNA-N
[SMILES]

O1C(=O)[C@]2([H])CCC[C@]2([H])C1=O |&1:3,8,r|
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H315-H318
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

38-41
[Safety Statements ]

26-39
[WGK Germany ]

3
[Storage Class]

13 - Non Combustible Solids
[Hazard Classifications]

Eye Dam. 1
Skin Irrit. 2
Hazard InformationBack Directory
[Uses]

cis-1,2-Cyclopentanedicarboxylic Anhydride functions as a reagent in the enantioselective synthesis of disubstituted proline derivatives and its application in synthesis of hepatitis C virus protease inhibitor telaprevir, Nrf2-Keap1 complex inhibitors preparation, binding mode and structural-activity relationship.
[Synthesis]

In a 250 ml aubergine flask, 2 g of cis-cyclopentyl-1,2dicarboxylic acid and 126.4 ml of acetic anhydride were added, heated and refluxed for 10 h. Excess acetic anhydride was removed under reduced pressure to obtain the crude cyclopentane-1,2-dicarboxyli
Spectrum DetailBack Directory
[Spectrum Detail]

CYCLOPENTANE-1,2-DICARBOXYLIC ACID ANHYDRIDE(35878-28-5)1HNMR
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