Home Quinolines 635-46-1
635-46-1,MFCD00006693
Catalog No.:AA003D7I

635-46-1 | 1,2,3,4-Tetrahydroquinoline

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10g
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$6.00   $4.00
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25g
98%
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$7.00   $5.00
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100g
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003D7I
Chemical Name:
1,2,3,4-Tetrahydroquinoline
CAS Number:
635-46-1
Molecular Formula:
C9H11N
Molecular Weight:
133.1903
MDL Number:
MFCD00006693
SMILES:
C1CCc2c(N1)cccc2
NSC Number:
15311
Properties
Properties
 
BP:
250.7°C at 760 mmHg  
Form:
Liquid  
MP:
9-14 °C(lit.)  
Refractive Index:
n20/D 1.593(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
111  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.3  

Upstream Synthesis Route

[1]HelveticaChimicaActa,1948,vol.31,p.924,925

[1]OrganicLetters,2016,vol.18,#24,p.6300-6303

[2]Tetrahedron,2017,vol.73,#36,p.5389-5396

[3]Arkivoc,2018,vol.2018,#3,p.362-374

[1]BioorganicandMedicinalChemistryLetters,2006,vol.16,#17,p.4533-4536

[2]Patent:US9522908,2016,B2,

[1]TetrahedronLetters,1986,vol.27,#38,p.4565-4568

[1]JournaloftheAmericanChemicalSociety,2012,vol.134,#42,p.17592-17598,7

[2]MolecularCatalysis,2018,vol.452,p.145-153

Downstream Synthesis Route

[1]ZhurnalObshcheiKhimii,1959,vol.29,p.1639,1641;engl.Ausg.S.1614

[1]HelveticaChimicaActa,1948,vol.31,p.924,925

[1]JournalofMedicinalChemistry,1989,vol.32,p.1927-1935

[2]Patent:US4587341,1986,A

[3]Patent:EP96214,1991,B1

[4]JournaloftheAmericanChemicalSociety,1953,vol.75,p.3029

[5]Patent:EP1666538,2006,A1.Locationinpatent:Page/Pagecolumn73-74

635-46-1    31827-94-8   
2-(3,4-dihydro-2<i>H</i>-1quinolyl)-1-(4-iodo-phenyl)-ethanone 

[1]JournaloftheAmericanChemicalSociety,1952,vol.74,p.4198

[1]JournaloftheChemicalSociety.PerkintransactionsI,1980,p.1933-1939

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Title: First QSAR report on FSH receptor antagonistic activity: quantitative investigations on physico-chemical and structural features among 6-amino-4-phenyltetrahydroquinoline derivatives.

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Title: Synthesis and SAR of cis-1-benzoyl-1,2,3,4-tetrahydroquinoline ligands for control of gene expression in ecdysone responsive systems.

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Journal: The Journal of organic chemistry 20020531

Title: Syntheses of fused heterocyclic compounds and their inhibitory activities for squalene synthase.

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Title: Combinatorial synthetic design. Solution and polymer-supported synthesis of heterocycles via intramolecular aza Diels-Alder and imino alcohol cyclizations.

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Title: First asymmetric synthesis of quinoline derivatives by inverse electron demand (IED) Diels-Alder reaction using chiral Ti(IV) complex.

Journal: Organic letters 20010628

Title: Asymmetric synthesis of functionalized 1,2,3,4-tetrahydroquinolines.

Journal: Organic letters 20010628

Title: Diastereoselective synthesis of substituted tetrahydroquinoline-4-carboxylic esters by a tandem reduction-reductive amination reaction.

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Title: Synthesis of a novel series of cytotoxic bisindole alkaloids.

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Title: Polymer-supported glyoxylate and alpha-imino acetates. Versatile reagents for the synthesis of alpha-hydroxycarboxylic acid and alpha-amino acid libraries.

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Tags:635-46-1 Molecular Formula|635-46-1 MDL|635-46-1 SMILES|635-46-1 1,2,3,4-Tetrahydroquinoline |Organic_Building_Blocks