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177478-49-8,MFCD08692534
Catalog No.:AA00259Z

177478-49-8 | Methyl 1,2,3,4-tetrahydroquinoline-6-carboxylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$17.00   $12.00
- +
250mg
97%
in stock  
$28.00   $20.00
- +
1g
97%
in stock  
$37.00   $26.00
- +
100g
97%
in stock  
$2,804.00   $1,963.00
- +
  • 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:
AA00259Z
Chemical Name:
Methyl 1,2,3,4-tetrahydroquinoline-6-carboxylate
CAS Number:
177478-49-8
Molecular Formula:
C11H13NO2
Molecular Weight:
191.2264
MDL Number:
MFCD08692534
SMILES:
COC(=O)c1ccc2c(c1)CCCN2
Properties
Properties
 
BP:
349.4°C at 760 mmHg  
Form:
Solid  
MP:
73-76°C  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
217  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
2.2  

Upstream Synthesis Route

[1]Chemistry-AEuropeanJournal,2017,vol.23,#57,p.14167-14172

[2]SyntheticCommunications,2018,vol.48,#11,p.1291-1298

[3]JournaloftheAmericanChemicalSociety,2015,vol.137,#33,p.10652-10658

[4]AdvancedSynthesisandCatalysis,2017,vol.359,#14,p.2358-2363

[5]AngewandteChemie-InternationalEdition,2017,vol.56,#11,p.3080-3084

[6]Angew.Chem.,2017,vol.129,#11,p.3126-3130,5

[7]ChemCatChem,2017,vol.9,#13,p.2463-2466

[8]OrganicLetters,2018,vol.20,#16,p.4723-4727

[1]CatalysisScienceandTechnology,2017,vol.7,#10,p.1981-1985

[2]CatalysisScienceandTechnology,2018,vol.8,#10,p.2648-2653

[3]Patent:CN105524053,2016,A,.Locationinpatent:Paragraph0534;0535;0536

[4]ACSCatalysis,2018,vol.8,#5,p.4545-4557

[5]AngewandteChemie-InternationalEdition,2017,vol.56,#12,p.3216-3220

[6]Angew.Chem.,2017,vol.129,#12,p.3264-3268,5

[7]Chemistry-AEuropeanJournal,2016,vol.22,#48,p.17151-17155

[8]OrganicLetters,2016,vol.18,#17,p.4250-4253

[9]ChemicalCommunications,2018,vol.54,#62,p.8622-8625

[10]Patent:CN108822030,2018,A,.Locationinpatent:Paragraph0035;0036;0037;0038

[11]AngewandteChemie-InternationalEdition,2016,vol.55,#1,p.292-296

[12]Angew.Chem.,2016,

[13]BioorganicandMedicinalChemistryLetters,2017,vol.27,#12,p.2781-2787

[14]ChemicalScience,2018,vol.9,#42,p.8134-8141

[15]Patent:WO2015/49535,2015,A1,.Locationinpatent:Paragraph00225

[16]Patent:US6300342,2001,B1,

[17]Patent:US2004/122001,2004,A1,

[18]Patent:WO2013/166013,2013,A1,.Locationinpatent:Paragraph0086;0087;0088

[19]ChemicalCommunications,2015,vol.51,#35,p.7558-7561

[20]GreenChemistry,2017,vol.19,#3,p.749-756

[21]AppliedCatalysisA:General,2018,vol.560,p.37-41

[1]JournalofOrganicChemistry,2002,vol.67,#22,p.7890-7893

[2]Patent:US2003/114679,2003,A1,

[3]ChemicalCommunications,2015,vol.51,#35,p.7558-7561

[1]Patent:WO2007/118137,2007,A1,.Locationinpatent:Page/Pagecolumn131

[2]Patent:WO2007/81335,2007,A1,.Locationinpatent:Page/Pagecolumn36-37

[1]BioorganicandMedicinalChemistryLetters,2011,vol.21,#2,p.670-676

[2]Patent:US2016/355483,2016,A1,.Locationinpatent:Paragraph0323-0324

Downstream Synthesis Route
32315-10-9    177478-49-8   
C13H12Cl3NO4 

[1]Patent:WO2007/118137,2007,A1.Locationinpatent:Page/Pagecolumn132

[1]Patent:US2006/178398,2006,A1.Locationinpatent:Page/Pagecolumn21-22

[1]Catalysisscienceandtechnology,2017,vol.7,p.1981-1985

[2]Catalysisscienceandtechnology,2018,vol.8,p.2648-2653

[3]Patent:CN105524053,2016,A.Locationinpatent:Paragraph0534;0535;0536

[4]ACSCatalysis,2018,vol.8,p.4545-4557

[5]AngewandteChemie-InternationalEdition,2017,vol.56,p.3216-3220    Angew.Chem.,2017,vol.129,p.3264-3268,5

[6]Chemistry-AEuropeanJournal,2016,vol.22,p.17151-17155

[7]OrganicLetters,2016,vol.18,p.4250-4253

[8]ChemicalCommunications,2018,vol.54,p.8622-8625

[9]Patent:CN108822030,2018,A.Locationinpatent:Paragraph0035;0036;0037;0038

[10]JournaloftheAmericanChemicalSociety,2019,vol.141,p.20424-20433

[11]Chemistry-AEuropeanJournal,2019,vol.25,p.238-245

[12]AngewandteChemie-InternationalEdition,2016,vol.55,p.292-296    Angew.Chem.,2016

[13]BioorganicandMedicinalChemistryLetters,2017,vol.27,p.2781-2787

[14]ChemicalScience,2018,vol.9,p.8134-8141

[15]Patent:WO2015/49535,2015,A1.Locationinpatent:Paragraph00225

[16]ACSCatalysis,2019,vol.9,p.7596-7606

[17]Patent:US6300342,2001,B1

[18]Patent:US2004/122001,2004,A1

[19]Patent:WO2013/166013,2013,A1.Locationinpatent:Paragraph0086;0087;0088

[20]ChemicalCommunications,2015,vol.51,p.7558-7561

[21]GreenChemistry,2017,vol.19,p.749-756

[22]AppliedCatalysisA:General,2018,vol.560,p.37-41

[23]Chemistry-AEuropeanJournal,2018,vol.24,p.3403-3407

[24]ChemicalScience,2019,vol.10,p.2193-2198

[1]Patent:US5994368,1999,A

[2]Patent:US6083961,2000,A

[1]Patent:WO2007/118137,2007,A1.Locationinpatent:Page/Pagecolumn131

[2]Patent:WO2007/81335,2007,A1.Locationinpatent:Page/Pagecolumn36-37

Literature
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SDS
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