+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
611-10-9,MFCD00001412
Catalog No.:AA0034RV

611-10-9 | Ethyl 2-oxocyclopentanecarboxylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
98%
in stock  
$6.00   $4.00
- +
25g
98%
in stock  
$13.00   $9.00
- +
100g
95%
in stock  
$32.00   $23.00
- +
500g
95%
in stock  
$78.00   $55.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
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
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:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.9  

Upstream Synthesis Route

[1]Patent:CN106866494,2017,A,

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

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

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

[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

[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

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

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

[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

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 611-10-9
10233-13-3

10233-13-3

 1139-13-5

1139-13-5

 117-47-5

117-47-5

 123-29-5

123-29-5

 123-66-0

123-66-0

 124-06-1

124-06-1
Building Blocks
More >
Tags:611-10-9 Molecular Formula|611-10-9 MDL|611-10-9 SMILES|611-10-9 Ethyl 2-oxocyclopentanecarboxylate
Catalog No.: AA0034RV
611-10-9,MFCD00001412
611-10-9 | Ethyl 2-oxocyclopentanecarboxylate
Pack Size： 10g
Purity： 98%
in stock
$6.00 $4.00
Pack Size： 25g
Purity： 98%
in stock
$13.00 $9.00
Pack Size： 100g
Purity： 95%
in stock
$32.00 $23.00
Pack Size： 500g
Purity： 95%
in stock
$78.00 $55.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
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;  
Complexity: 174  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 1  
Undefined Bond Stereocenter Count: 0  
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 fold

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

Journal: The Journal of organic chemistry20110715

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 chemistry20051111

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

Journal: Physical chemistry chemical physics : PCCP20050707

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

Journal: The Journal of organic chemistry20041001

Title: Hydrogenation of cinchona alkaloids over supported Pt catalyst.

Journal: Chirality20030101

Title: Enantioselective Michael addition catalyzed by cinchona alkaloids.

Journal: Chirality20010101

Related Products of of 611-10-9
10233-13-3
10233-13-3
1139-13-5
1139-13-5
117-47-5
117-47-5
123-29-5
123-29-5
123-66-0
123-66-0
124-06-1
124-06-1
Building Blocks More >
12093-10-6
12093-10-6
Ferrocenecarboxaldehyde
AA0034UQ | MFCD00001429
10525-37-8
10525-37-8
Icosan-1-amine
AA0034XN | MFCD08272121
7550-35-8
7550-35-8
Lithium Bromide
AA00350U | MFCD00149763
1354940-69-4
1354940-69-4
Methyl 3-aminocyclobutanecarboxylate hydrochloride
AA00353T | MFCD17015886
122-07-6
122-07-6
Methylaminoacetaldehyde dimethyl acetal
AA00356M | MFCD00008485
473923-56-7
473923-56-7
tert-Butyl 3-(hydroxymethyl)morpholine-4-carboxylate
AA00359T | MFCD04038649
112-90-3
112-90-3
Oleylamine, tech grade
AA0035CQ | MFCD00066507
67627-18-3
67627-18-3
Potassium Indigotrisulfonate
AA0035FS | MFCD00013160
7775-14-6
7775-14-6
Sodium hydrosulfite
AA0035IT | MFCD00011640
32503-27-8
32503-27-8
Tetrabutylammonium hydrogen sulfate
AA0035LS | MFCD00011637
Submit
© 2017 AA BLOCKS, INC. All rights reserved.