Home Quinolines 52601-70-4
52601-70-4,MFCD00218100
Catalog No.:AA00D82Y

52601-70-4 | 8-methyl-1,2,3,4-tetrahydroquinoline

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100mg
95%
in stock  
$26.00   $18.00
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250mg
95%
in stock  
$42.00   $29.00
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1g
95%
in stock  
$58.00   $41.00
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25g
98%
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$1,341.00   $939.00
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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:
AA00D82Y
Chemical Name:
8-methyl-1,2,3,4-tetrahydroquinoline
CAS Number:
52601-70-4
Molecular Formula:
C10H13N
Molecular Weight:
147.2169
MDL Number:
MFCD00218100
SMILES:
Cc1cccc2c1NCCC2
Properties
Computed Properties
 
Complexity:
133  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.7  

Upstream Synthesis Route

[1]Molecules,2015,vol.20,#10,p.18661-18684

[2]AdvancedSynthesisandCatalysis,2017,vol.359,#6,p.933-940

[3]ChemicalCommunications,2013,vol.49,#63,p.7052-7054

[4]AdvancedSynthesisandCatalysis,2016,vol.358,#19,p.3039-3045

[5]Patent:CN106831565,2017,A,.Locationinpatent:Paragraph0079;0080;0081;0082

[6]Tetrahedron,2018,vol.74,#17,p.2121-2129

[7]ChemCatChem,2013,vol.5,#8,p.2183-2186

[8]JournalofOrganometallicChemistry,2016,vol.821,p.197-205

[9]JournaloftheAmericanChemicalSociety,2015,vol.137,#36,p.11718-11724

[10]ACSCatalysis,2016,vol.6,#9,p.5816-5822

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

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

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

[14]AdvancedSynthesisandCatalysis,2017,vol.359,#4,p.677-686

[15]TetrahedronLetters,1987,vol.28,#1,p.77-80

[16]BulletinoftheChemicalSocietyofJapan,1989,vol.62,#9,p.2968-2976

[17]ChemCatChem,2017,vol.9,#13,p.2496-2505

[18]AngewandteChemie-InternationalEdition,2016,vol.55,#40,p.12224-12227

[19]Angew.Chem.,2016,vol.128,#40,p.12412-12415,4

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

[21]ChemicalCommunications,2010,vol.46,#27,p.4884-4886

[22]ChemicalScience,2015,vol.6,#3,p.2010-2015

[23]AngewandteChemie-InternationalEdition,2015,vol.54,#8,p.2467-2471

[24]TetrahedronLetters,2017,vol.58,#36,p.3571-3573

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

[26]Angew.Chem.,2016,

[27]ChemistryLetters,2010,vol.39,#8,p.832-834

[28]Chemistry-AEuropeanJournal,2012,vol.18,#2,p.574-585

[29]OrganicLetters,2013,vol.15,#7,p.1484-1487

[30]TetrahedronLetters,2004,vol.45,#16,p.3215-3217

[31]AppliedCatalysisA:General,2015,vol.499,p.118-123

[32]AppliedOrganometallicChemistry,2018,vol.32,#4,

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

[34]Patent:CN106432072,2017,A,.Locationinpatent:Paragraph0044-0055

[35]JournaloftheAmericanChemicalSociety,2014,vol.136,#24,p.8564-8567

[36]OrganicandBiomolecularChemistry,2012,vol.10,#9,p.1826-1833

[37]AngewandteChemie-InternationalEdition,2018,vol.57,#18,p.4970-4975

[38]Angew.Chem.,2018,vol.130,#18,p.5064-5069,6

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

[40]JournalofMolecularCatalysisA:Chemical,2015,vol.402,p.83-91

[41]ChemischeBerichte,1891,vol.24,p.2051

[42]ChemischeBerichte,1888,vol.21,p.866

[43]ChemischeBerichte,1923,vol.56,p.1343

[44]ChemischeBerichte,1923,vol.56,p.1343

[45]JournalofOrganicChemistry,1957,vol.22,p.571,573

[46]Patent:US2881061,1956,,

[47]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1980,p.1933-1939

[48]Organometallics,2011,vol.30,#17,p.4497-4500

[49]JournaloftheAmericanChemicalSociety,2012,vol.134,#38,p.15728-15731,4

[50]DaltonTransactions,2012,vol.41,#48,p.14490-14497

[51]JournalofCatalysis,2013,vol.297,p.272-280

[52]OrganicandBiomolecularChemistry,2013,vol.11,#7,p.1209-1215

[53]AppliedCatalysisA:General,2014,vol.481,p.89-95

[54]CatalysisScienceandTechnology,2015,vol.5,#7,p.3728-3734

[55]AngewandteChemie-InternationalEdition,2014,vol.53,#38,p.10218-10222

[56]Angew.Chem.,2014,vol.126,#38,p.10382-10386,5

[57]CatalysisScienceandTechnology,2015,vol.5,#10,p.4746-4749

[58]TetrahedronLetters,2016,vol.57,#3,p.329-332

[59]CatalysisScienceandTechnology,2017,vol.7,#11,p.2221-2227

[60]ACSCatalysis,2018,vol.8,#1,p.17-21

[61]TetrahedronLetters,2018,vol.59,#10,p.949-953

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

[63]CatalysisScienceandTechnology,2018,vol.8,#19,p.5019-5097

[64]NewJournalofChemistry,2018,vol.42,#20,p.16694-16702

[65]ChemCatChem,2018,vol.10,#21,p.4980-4986

[1]JournalofOrganicChemistry,1983,vol.48,#22,p.4053-4058

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

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1980,p.1933-1939

[2]CatalysisLetters,2018,vol.148,#5,p.1336-1344

[1]JournalofOrganicChemistry,1983,vol.48,#22,p.4053-4058

Downstream Synthesis Route
52601-70-4    506-68-3   
1,5-bis-(8-methyl-3,4-dihydro-2<i>H</i>-1quinolyl)-pentamethinium;bromide 

[1]JournalfurpraktischeChemie(Leipzig1954),1912,vol.&lt;2&gt;85,p.377

[1]ChemischeBerichte,1894,vol.27,p.825

[1]ChemischeBerichte,1913,vol.46,p.1280

52601-70-4    98-74-8   
8-methyl-1-(4-nitro-benzenesulfonyl)-1,2,3,4-tetrahydro-quinoline 

[1]JournaloftheAmericanChemicalSociety,1952,vol.74,p.5961

52601-70-4    121-60-8   
1-(<i>N</i>-acetyl-sulfanilyl)-8-methyl-1,2,3,4-tetrahydro-quinoline 

[1]JournaloftheAmericanChemicalSociety,1952,vol.74,p.5961

Literature
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