Catalog No.:AA0034RV

611-10-9 | Ethyl 2-oxocyclopentanecarboxylate

Name: Name:Ethyl 2-oxocyclopentanecarboxylate
Brand: AABLOCKS
SKU: AA0034RV
Availability: InStock
Rating: 90 (10 reviews)

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10g

98%

in stock

$6.00 $4.00

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25g

98%

in stock

$13.00 $9.00

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100g

95%

in stock

$32.00 $23.00

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500g

95%

in stock

$78.00 $55.00

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
Download SDS

Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA0034RV

Chemical Name:

Ethyl 2-oxocyclopentanecarboxylate

CAS Number:

611-10-9

Molecular Formula:

C8H12O3

Molecular Weight:

156.1791

MDL Number:

MFCD00001412

SMILES:

CCOC(=O)C1CCCC1=O

Properties

BP:

228.2°C at 760 mmHg

Form:

Liquid

Refractive Index:

n20/D 1.452(lit.)

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

174

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Undefined Atom Stereocenter Count:

XLogP3:

0.9

Upstream Synthesis Route

611-10-9

1468-87-7

[1]Patent:CN106866494,2017,A,

611-10-9

5661-01-8

[1]JournaloftheAmericanChemicalSociety,1959,vol.81,p.3108,3111

611-10-9

56946-65-7

[1]HelveticaChimicaActa,1945,vol.28,p.1684,1690

611-10-9

57-13-6

5466-43-3

[1]Patent:US2008/132490,2008,A1,.Locationinpatent:Page/Pagecolumn20-21

611-10-9

5466-43-3

[1]JournalofMedicinalChemistry,1994,vol.37,#22,p.3828-3833

[2]EuropeanJournalofMedicinalChemistry,1980,vol.15,#4,p.317-322

[3]Patent:WO2014/15291,2014,A1,

[4]Patent:US2014/179668,2014,A1,

[5]Patent:WO2015/28848,2015,A1,

[6]EuropeanJournalofMedicinalChemistry,2015,vol.92,p.246-256

[7]Patent:US2016/90374,2016,A1,

[8]Patent:WO2008/112913,2008,A1,

Downstream Synthesis Route

141-28-6

611-10-9

[1]Patent:US2006/79709,2006,A1.Locationinpatent:Page/Pagecolumn4

[2]Patent:US2006/79709,2006,A1.Locationinpatent:Page/Pagecolumn3-4

[3]JournaloftheChemicalSociety.PerkintransactionsI,1998,p.3521-3522

[4]Tetrahedron,1998,vol.54,p.10827-10836

[5]Patent:EP2248796,2010,A1.Locationinpatent:Page/Pagecolumn16-17

[6]Patent:US2011/60054,2011,A1.Locationinpatent:Page/Pagecolumn12

[7]TetrahedronLetters,1984,vol.25,p.753-756

[8]ChemischeBerichte,1894,vol.27,p.103 JustusLiebigsAnnalenderChemie,1901,vol.317,p.47,93

[9]BulletindelaSocieteChimiquedeFrance,1899,vol.<3>21,p.1022

[10]JustusLiebigsAnnalenderChemie,1901,vol.317,p.104

[11]JournaloftheChemicalSociety,1934,p.935,942

[12]ActaChemicaScandinavica(1947),1948,vol.2,p.385,386

[13]JournaloftheChemicalSociety,1934,p.935,942

[14]BulletinoftheChemicalSocietyofJapan,1996,vol.69,p.2619-2624

[15]JournaloftheSerbianChemicalSociety,2013,vol.78,p.759-768+S57-S61

[16]RSCAdvances,2014,vol.4,p.44350-44358

50-00-0

6091-44-7

611-10-9

2-oxo-1-piperidinomethyl-cyclopentanecarboxylicacidethylester

[1]ArchivderPharmazie,1942,vol.280,p.361,371

101860-81-5

611-10-9

101584-95-6

[1]JournalofOrganicChemistry,1957,vol.22,p.630

611-10-9

7394-79-8

[1]CanadianJournalofResearch,SectionB:ChemicalSciences,1936,vol.14,p.1,5

141-52-6

611-10-9

4296-15-5

6453-13-0

[1]BulletinoftheChemicalSocietyofJapan,1966,vol.39,p.530-535

Literature

Title: Cu(I)- and Cu(II)-catalyzed cyclo- and Michael addition reactions of unsaturated β-ketoesters.

Journal: The Journal of organic chemistry 20110715

Title: From cyclopentanone oximes to bis[1,2,3]dithiazolo-s-indacenes, cyclopenta[c][1,2]thiazine, pentathiepino-, tetrathiino-, and thienocyclopenta[1,2,3]dithiazoles as a rich source of new materials.

Journal: The Journal of organic chemistry 20051111

Title: Investigations into the metal species of the homogeneous iron(III) catalyzed Michael addition reactions.

Journal: Physical chemistry chemical physics : PCCP 20050707

Title: Synthesis of bicyclo[4.n.1]alkanones.

Journal: The Journal of organic chemistry 20041001

Title: Hydrogenation of cinchona alkaloids over supported Pt catalyst.

Journal: Chirality 20030101

Title: Enantioselective Michael addition catalyzed by cinchona alkaloids.

Journal: Chirality 20010101

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SDS