Home Aldehydes 2987-17-9
2987-17-9,MFCD03789631
Catalog No.:AA003643

2987-17-9 | Cyclobutanecarboxaldehyde

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1g
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$18.00   $13.00
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5g
95%
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$34.00   $24.00
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10g
95%
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$65.00   $46.00
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25g
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50g
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003643
Chemical Name:
Cyclobutanecarboxaldehyde
CAS Number:
2987-17-9
Molecular Formula:
C5H8O
Molecular Weight:
84.1164
MDL Number:
MFCD03789631
SMILES:
O=CC1CCC1
Properties
Properties
 
BP:
105.412°C at 760mmHg  
Form:
Liquid  
Storage:
-20 ℃;Light sensitive;Inert atmosphere;  

Computed Properties
 
Complexity:
55  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
0.7  

Downstream Synthesis Route

[1]ZhurnalObshcheiKhimii,1953,vol.23,p.1994,1996;engl.Ausg.S.2109,2110

[1]JournalofMedicinalChemistry,1981,vol.24,p.7-12

[2]Patent:WO2008/82486,2008,A2.Locationinpatent:Page/Pagecolumn3;11;18;20;25;38;40;43

[3]Patent:WO2011/31554,2011,A2.Locationinpatent:Page/Pagecolumn166

[4]Patent:US2011/207754,2011,A1.Locationinpatent:Page/Pagecolumn10

[5]TetrahedronLetters,1981,vol.22,p.3439-3442

[6]JournaloftheChemicalSociety.PerkintransactionsII,1990,p.1997-2007

[7]JournalofOrganicChemistry,2009,vol.74,p.1567-1573

[8]ZhurnalObshcheiKhimii,1938,vol.8,p.1179,1188    ChemischesZentralblatt,1940,vol.111,p.1490

[9]HelveticaChimicaActa,1969,vol.52,p.1146-1156

[10]AngewandteChemie-InternationalEdition,2001,vol.40,p.1064-1065

[11]HelveticaChimicaActa,2003,vol.86,p.865-893

[12]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.732-737

[13]Patent:WO2008/54698,2008,A2.Locationinpatent:Page/Pagecolumn36

[14]EuropeanJournalofOrganicChemistry,2009,p.1707-1719

[15]Tetrahedron,2009,vol.65,p.7372-7379

[16]JournalofOrganicChemistry,2009,vol.74,p.7866-7872

[17]Patent:WO2013/19828,2013,A1.Locationinpatent:Page/Pagecolumn74

[18]Patent:US2013/79412,2013,A1.Locationinpatent:Paragraph0365

[19]Patent:WO2014/100071,2014,A2.Locationinpatent:Page/Pagecolumn76

[20]Patent:WO2014/123882,2014,A1.Locationinpatent:Page/Pagecolumn67

[21]Patent:WO2014/120748,2014,A1.Locationinpatent:Page/Pagecolumn149

[22]Patent:WO2014/140076,2014,A1.Locationinpatent:Page/Pagecolumn71

[23]Patent:WO2014/190271,2014,A2.Locationinpatent:Page/Pagecolumn45

[24]Patent:WO2014/190270,2014,A1.Locationinpatent:Page/Pagecolumn58

[25]Patent:WO2016/4272,2016,A1.Locationinpatent:Paragraph00633

[26]JournalofOrganicChemistry,2016,vol.81,p.2189-2193

[27]BioorganicandMedicinalChemistryLetters,2016,vol.26,p.5871-5876

[28]ACSMedicinalChemistryLetters,2017,vol.8,p.256-260

[29]Patent:WO2008/116338,2008,A2.Locationinpatent:Page/Pagecolumn40

[1]ZhurnalObshcheiKhimii,1938,vol.8,p.1179,1188    ChemischesZentralblatt,1940,vol.111,p.1490

[2]JournaloftheAmericanChemicalSociety,1958,vol.80,p.5378,5380

[3]ChemischeBerichte,1967,vol.100,p.1465-1473

[4]JournalofMedicinalChemistry,1989,vol.32,p.1001-1006

[5]JournalofOrganicChemistry,1973,vol.38,p.1463-1469

[6]Patent:WO2006/35195,2006,A1.Locationinpatent:Page/Pagecolumn8

[7]Patent:US4499296,1985,A

[1]Demjanow;Dojarenko[ChemischeBerichte,1922,vol.55,p.2725]

[1]Journalofmedicinalandpharmaceuticalchemistry,1961,vol.4,p.517-534

Literature

Title: Steric effects on the enantiodiscrimination of diproline chiral stationary phases in the resolution of racemic compounds.

Journal: Journal of chromatography. A 20110812

Title: Reactions of monoaryl-substituted methylenecyclobutanes and methylenecyclopropanes with 1-hydroxybenzotriazole (HOBt), 1-hydroxy-7-azabenzotriazole (HOAt), and 1-hydroxysuccinimide (HOSu).

Journal: The Journal of organic chemistry 20090320

Title: Atmospheric chemistry of C3-C6 cycloalkanecarbaldehydes.

Journal: The journal of physical chemistry. A 20050616

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SDS
Tags:2987-17-9 Molecular Formula|2987-17-9 MDL|2987-17-9 SMILES|2987-17-9 Cyclobutanecarboxaldehyde