Catalog No.:AA003TN1

3297-72-1 | 1-Phenylisoquinoline

Name: Name:1-Phenylisoquinoline
Brand: AABLOCKS
SKU: AA003TN1
Availability: InStock
Rating: 90 (10 reviews)

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250mg

98%

in stock

$12.00 $8.00

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98%

in stock

$32.00 $22.00

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98%

in stock

$121.00 $85.00

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003TN1

Chemical Name:

1-Phenylisoquinoline

CAS Number:

3297-72-1

Molecular Formula:

C15H11N

Molecular Weight:

205.2545

MDL Number:

MFCD00093934

SMILES:

c1ccc(cc1)c1nccc2c1cccc2

Properties

BP:

347.6°C at 760 mmHg

Form:

Solid

MP:

96 °C

Refractive Index:

1.6550 (estimate)

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

220

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

3.8

Downstream Synthesis Route

52250-50-7

3297-72-1

[1]Liang,Bo;Jiang,Changyun;Chen,Zhao;Zhang,Xiuju;Shi,Huahong;Cao,Yong[JournalofMaterialsChemistry,2006,vol.16,#13,p.1281-1286]

[2]Movassaghi,Mohammad;Hill,MatthewD.[OrganicLetters,2008,vol.10,#16,p.3485-3488]

[3]Pictet;Kay[ChemischeBerichte,1909,vol.42,p.1977]

[4]Asthana;Misra[JournaloftheIndianChemicalSociety,1951,vol.28,p.483,484]

[5]Rodionow;Jaworskaja[ZhurnalObshcheiKhimii,1941,vol.11,p.446,448][Chem.Abstr.,1941,p.6592]

[6]Spaethetal.[ChemischeBerichte,1930,vol.63,p.134,136]

[7]Yang,Cheng-Hsien;Tai,Chia-Cheng;Sun,I.-Wen[JournalofMaterialsChemistry,2004,vol.14,#6,p.947-950]

[8]Cherest,M.;Lusinchi,X.[Tetrahedron,1982,vol.38,#23,p.3471-3478]

52250-50-7

3297-72-1

22990-19-8

[1]JournaloftheChemicalSociety,1949,p.2587

[2]JournaloftheChemicalSociety,1949,p.2587

52250-50-7

3297-72-1

86448-84-2

[1]Cherest,M.;Lusinchi,X.[Tetrahedron,1982,vol.38,#23,p.3471-3478]

1-phenyl-2-tosyl-1,2,3,4-tetrahydroisoquinoline

3297-72-1

[1]EuropeanJournalofOrganicChemistry,2010,p.6987-6992

[2]Patent:CN106831881,2017,A.Locationinpatent:Paragraph0104;0105;0128;0129

[3]Synlett,2002,p.907-910

[4]EuropeanJournalofMedicinalChemistry,2020,vol.203

19493-44-8

98-80-6

3297-72-1

[1]AngewandteChemie-InternationalEdition,2005,vol.44,p.2444-2447

[2]EuropeanJournalofOrganicChemistry,2012,p.6248-6259,12

[3]DaltonTransactions,2018,vol.47,p.3803-3810

[4]JournalofChemicalSciences,2017,vol.129,p.1391-1398

[5]Patent:EP1555269,2005,A1.Locationinpatent:Page/Pagecolumn8;9;10;11

[6]BulletinoftheKoreanChemicalSociety,2010,vol.31,p.3010-3012

[7]AdvancedSynthesisandCatalysis,2018,vol.360,p.3990-3998

[8]EuropeanJournalofInorganicChemistry,2008,p.2177-2185

[9]AdvancedSynthesisandCatalysis,2010,vol.352,p.201-211

[10]Patent:US2006/36097,2006,A1.Locationinpatent:Page/Pagecolumn8-9

[11]DaltonTransactions,2013,vol.42,p.13612-13621

[12]Macromolecules,2005,vol.38,p.4072-4080

[13]JournaloftheAmericanChemicalSociety,2003,vol.125,p.12971-12979

[14]Patent:WO2004/60876,2004,A1.Locationinpatent:Page8-9

[15]JournalofOrganometallicChemistry,2002,vol.663,p.46-57

[16]DaltonTransactions,2005,p.1583-1590

[17]Tetrahedron,2006,vol.62,p.11483-11498

[18]Patent:US2007/176542,2007,A1.Locationinpatent:Page/Pagecolumn9

[19]Chemistry-AEuropeanJournal,2011,vol.17,p.130-142

[20]Patent:US2012/261651,2012,A1

[21]JournaloftheAmericanChemicalSociety,2013,vol.135,p.9322-9325

[22]Chemistry-AnAsianJournal,2013,vol.8,p.2575-2578

[23]Patent:CN109053813,2018,A.Locationinpatent:Paragraph0106-0108

[24]Patent:CN109467576,2019,A.Locationinpatent:Paragraph0020

Literature

Title: 1,12-diazaperylene and 2,11-dialkylated-1,12-diazaperylene iridium(III) complexes [Ir(C^N)2(N^N)]PF6: new supramolecular assemblies.

Journal: Dalton transactions (Cambridge, England : 2003) 20120914

Title: Acid induced acetylacetonato replacement in biscyclometalated iridium(III) complexes.

Journal: Dalton transactions (Cambridge, England : 2003) 20120407

Title: 1-Phenylisoquinoline larvicidal activity against Culex quinquefasciatus.

Journal: Natural product research 20120101

Title: NMR study on iridium(III) complexes for identifying disulfonate substituted bathophenanthroline regio-isomers.

Journal: Magnetic resonance in chemistry : MRC 20111201

Title: High-efficiency red phosphorescent electroluminescence devices based on mixed p/n host matrices.

Journal: Optics letters 20101001

Title: Zwitterionic iridium complexes: synthesis, luminescent properties, and their application in cell imaging.

Journal: Inorganic chemistry 20100405

Title: Synthesis of quinolinyl and isoquinolinyl phenyl ketones as novel agonists for the cannabinoid CB2 receptor.

Journal: Bioorganic & medicinal chemistry 20090701

Title: Syntheses, photophysics, and application of iridium(III) phosphorescent emitters for highly efficient, long-life organic light-emitting diodes.

Journal: Chemistry, an Asian journal 20090504

Title: High-efficiency electrophosphorescent copolymers containing charged iridium complexes in the side chains.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

Title: Narrow-line and broadband spectra of iridium(III) complexes in a Shpol'skii matrix and an amorphous host.

Journal: The journal of physical chemistry. A 20060817

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Title: Substituent effects of iridium complexes for highly efficient red OLEDs.

Journal: Dalton transactions (Cambridge, England : 2003) 20050505

Title: Stereocontrolled synthesis of cis-dibenzoquinolizine chlorofumarates: curare-like agents of ultrashort duration.

Journal: The Journal of organic chemistry 20010518

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