+1 858-523-8231
Login | Register
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
Home Other Building Blocks 1759-68-8
1759-68-8,MFCD00452187
Catalog No.:AA01AC88

1759-68-8 | N-cyclohexylbenzamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
99%
in stock  
$43.00   $30.00
- +
1g
99%
in stock  
$72.00   $50.00
- +
5g
99%
in stock  
$186.00   $130.00
- +
25g
99%
in stock  
$529.00   $370.00
- +
100g
99%
in stock  
$1,729.00   $1,210.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA01AC88
Chemical Name:
N-cyclohexylbenzamide
CAS Number:
1759-68-8
Molecular Formula:
C13H17NO
Molecular Weight:
203.2802
MDL Number:
MFCD00452187
SMILES:
O=C(c1ccccc1)NC1CCCCC1
NSC Number:
4632
Properties
Computed Properties
 
Complexity:
203  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
2.9  

Downstream Synthesis Route

[1]JournalofOrganicChemistry,2016,vol.81,p.4235-4243

[2]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12817-12819

[3]JournalofOrganicChemistry,2019

[4]JournalofOrganicChemistry,2019,vol.84,p.6084-6093

[5]Patent:CN110818576,2020,A.Locationinpatent:Paragraph0070;0071;0072;0073;0074;0075;0076

[6]AdvancedSynthesisandCatalysis,2013,vol.355,p.2775-2780

[7]ChemicalCommunications,2012,vol.48,p.2683-2685

[8]ACSCatalysis,2018,vol.8,p.8014-8019

[9]ChemCatChem,2017,vol.9,p.2009-2017

[10]JournalofOrganicChemistry,1953,vol.18,p.1190,1196

[11]OrganicLetters,2020,vol.22,p.1306-1310

[1]AngewandteChemie-InternationalEdition,2014,vol.53,p.9068-9071    Angew.Chem.,2014,vol.126,p.9214-9217,4

[2]ChemischeBerichte,1962,vol.95,p.126-136

[3]ChemischeBerichte,1962,vol.95,p.126-136

[4]JournalofOrganicChemistry,2010,vol.75,p.7408-7411

[5]ChemicalCommunications,2013,vol.49,p.5313-5315

[6]OrganicLetters,2013,vol.15,p.2668-2671

[7]Patent:DE715543,1938,C

[1]JournalofOrganicChemistry,2021,vol.86,p.2339-2358

[2]ChemicalCommunications,2008,p.1100-1102

[3]AdvancedSynthesisandCatalysis,2021,vol.363,p.2529-2535

[4]AppliedOrganometallicChemistry,2020,vol.34

[5]ChemischesZentralblatt,1919,vol.90,p.952

[6]ChemischesZentralblatt,1919,vol.90,p.952

[7]GreenChemistry,2011,vol.13,p.1791-1798

[1]ChemistryLetters,2017,vol.46,p.560-562

[2]TetrahedronLetters,2018,vol.59,p.991-994

[3]JournaloftheChemicalSociety,1945,p.660,662

[1]EuropeanJournalofMedicinalChemistry,1986,vol.21,p.181-185

[2]OrganicLetters,2003,vol.5,p.4241-4244

[3]Organicletters,2003,vol.5,p.105-107

[4]JournaloftheAmericanChemicalSociety,2010,vol.132,p.12817-12819

[5]Patent:WO2006/8556,2006,A1.Locationinpatent:Page/Pagecolumn17

[6]TetrahedronLetters,2006,vol.47,p.6429-6432

[7]TetrahedronLetters,2010,vol.51,p.6049-6051

[8]AngewandteChemie-InternationalEdition,2018,vol.57,p.15762-15766    Angew.Chem.,2018,vol.130,p.15988-15992,5

[9]JournaloftheAmericanChemicalSociety,2021,vol.143,p.5022-5037

[10]SyntheticCommunications,1982,vol.12,p.709-714

[11]OrganicLetters,2019,vol.21,p.3808-3812

[12]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.7169-7174

[13]JournalofHeterocyclicChemistry,2002,vol.39,p.1219-1227

[14]TetrahedronLetters,2010,vol.51,p.1434-1436

[15]AngewandteChemie-InternationalEdition,2014,vol.53,p.9068-9071    Angew.Chem.,2014,vol.126,p.9214-9217,4

[16]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.3307-3309

[17]HelveticaChimicaActa,2006,vol.89,p.532-536

[18]AdvancedSynthesisandCatalysis,2018,vol.360,p.2324-2332

[19]Patent:WO2006/2474,2006,A1.Locationinpatent:Page/Pagecolumn172

[20]Patent:US2008/153802,2008,A1.Locationinpatent:Page/Pagecolumn85-86

[21]Molecules,2003,vol.8,p.374-380

[22]OrganicPreparationsandProceduresInternational,2021,vol.53,p.301-310

[23]OrganicLetters,2020,vol.22,p.1306-1310

[24]SyntheticCommunications,2008,vol.38,p.4068-4075

[25]JustusLiebigsAnnalenderChemie,1894,vol.278,p.108

[26]TetrahedronLetters,1999,vol.40,p.5323-5326

[27]JournaloftheChemicalSociety.PerkintransactionsI,1999,p.3139-3142

[28]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2010,vol.49,p.1225-1228

[29]ChemicalCommunications,2012,vol.48,p.2683-2685

[30]AngewandteChemie-InternationalEdition,2012,vol.51,p.9904-9908

[31]Chemistry-AEuropeanJournal,2013,vol.19,p.7328-7333

[32]AngewandteChemie-InternationalEdition,2013,vol.52,p.8031-8036    Angew.Chem.,2013,vol.125,p.8189-8194,6

[33]JournalofOrganicChemistry,2017,vol.82,p.420-430

[34]OrganicLetters,2018,vol.20,p.2468-2471

[35]Chemistry-AEuropeanJournal,2021,vol.27,p.7915-7922

[36]Chemistry-AEuropeanJournal,2021,vol.27,p.17952-17959

[37]JournalofOrganicChemistry,2022,vol.87,p.4918-4925

[38]Synthesis,2022

Literature

Title: N-Cyclo-hexyl-benzamide.

Journal: Acta crystallographica. Section E, Structure reports online 20100701

Title: Novel 2- and 4-substituted 1H-imidazo[4,5-c]quinolin-4-amine derivatives as allosteric modulators of the A3 adenosine receptor.

Journal: Journal of medicinal chemistry 20090409

Title: Discovery and optimization of piperidyl benzamide derivatives as a novel class of 11beta-HSD1 inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20090315

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 1759-68-8
150514-60-6

150514-60-6

 15088-29-6

15088-29-6

 159180-70-8

159180-70-8

 17675-42-2

17675-42-2

 23062-17-1

23062-17-1

 292635-34-8

292635-34-8
Building Blocks
More >
Tags:1759-68-8 Molecular Formula|1759-68-8 MDL|1759-68-8 SMILES|1759-68-8 N-cyclohexylbenzamide