Catalog No.:AA00EKLT

5784-95-2 | 2-(4-Methoxyphenyl)-1h-indole

Name: Name:2-(4-Methoxyphenyl)-1h-indole
Brand: AABLOCKS
SKU: AA00EKLT
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250mg

97%

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$96.00 $67.00

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>98.0%(GC)

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$184.00 $129.00

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>98.0%(GC)

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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:

AA00EKLT

Chemical Name:

2-(4-Methoxyphenyl)-1h-indole

CAS Number:

5784-95-2

Molecular Formula:

C15H13NO

Molecular Weight:

223.2698

MDL Number:

MFCD00443483

SMILES:

COc1ccc(cc1)c1cc2c([nH]1)cccc2

Properties

Form:

Solid

MP:

229.0 to 233.0 °C

Storage:

2-8℃;

Computed Properties

Complexity:

247

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

3.8

Downstream Synthesis Route

157869-15-3

5784-95-2

[1]Tetrahedron,2012,vol.68,p.1393-1400

[2]AdvancedSynthesisandCatalysis,2016,vol.358,p.3313-3318

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[4]OrganicandBiomolecularChemistry,2011,vol.9,p.4983-4986

[5]AngewandteChemie-InternationalEdition,2013,vol.52,p.11835-11839 Angew.Chem.,2013,vol.125,p.12051-12055,5

[6]TetrahedronLetters,2009,vol.50,p.6877-6881

[7]Tetrahedron,2010,vol.66,p.7169-7178

[8]EuropeanJournalofOrganicChemistry,2007,p.5332-5335

[9]JournalofOrganometallicChemistry,1994,vol.475,p.289-296

[10]JournalofOrganometallicChemistry,2010,vol.695,p.1675-1681

[11]BeilsteinJournalofOrganicChemistry,2011,vol.7,p.565-569

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[13]AngewandteChemie-InternationalEdition,2019,vol.58,p.7687-7691 Angew.Chem.,2019,vol.131,p.7769-7773,5

5784-95-2

33513-42-7

76195-80-7

[1]ResearchonChemicalIntermediates,2019,vol.45,p.2827-2854

[2]Chemistryandbiodiversity,2019,vol.16

[3]ResearchonChemicalIntermediates,2019,vol.45,p.5261-5290

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[5]PharmaceuticalChemistryJournal,1994,vol.28,p.751-755 Khimiko-FarmatsevticheskiiZhurnal,1994,vol.28,p.47-50

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[8]MedicinalChemistryResearch,2012,vol.21,p.3406-3416

[9]EuropeanJournalofMedicinalChemistry,2017,vol.136,p.184-194

[10]OrganicLetters,2019,vol.21,p.2602-2605

[11]JournalofHeterocyclicChemistry,2019,vol.56,p.3303-3312

[12]BioorganicChemistry,2020,vol.99

100-63-0

100-06-1

5784-95-2

[1]PharmaceuticalChemistryJournal,1994,vol.28,p.751-755 Khimiko-FarmatsevticheskiiZhurnal,1994,vol.28,p.47-50

[2]BioorganicandMedicinalChemistryLetters,2013,vol.23,p.2671-2674

[3]SyntheticCommunications,2019,vol.49,p.2258-2269

[4]JournalofMedicinalChemistry,2015,vol.58,p.2206-2220

[5]ResearchonChemicalIntermediates,2019,vol.45,p.2827-2854

[6]Chemistryandbiodiversity,2019,vol.16

[7]OrganicLetters,2019,vol.21,p.3687-3691

[8]ResearchonChemicalIntermediates,2019,vol.45,p.5261-5290

[9]JournalofHeterocyclicChemistry,2019,vol.56,p.3303-3312

[10]BioorganicChemistry,2020,vol.99

[11]ChemicalCommunications,2021,vol.57,p.10242-10245

112768-16-8

5784-95-2

[1]EuropeanJournalofOrganicChemistry,2020,vol.2020,p.57-60

[2]TetrahedronLetters,1999,vol.40,p.5717-5720

5784-95-2

54888-60-7

[1]JournaloftheAmericanChemicalSociety,2013,vol.135,p.11740-11743

[2]Tetrahedron,2002,vol.58,p.9187-9191

[3]OrganicLetters,2009,vol.11,p.1789-1791

[4]AngewandteChemie-InternationalEdition,2016,vol.55,p.3148-3152 Angew.Chem.,2016,vol.128,p.3200-3204,5

[5]TetrahedronLetters,2017,vol.58,p.2993-2996

Literature

Title: Oxidative coupling as a biomimetic approach to the synthesis of scytonemin.

Journal: Organic letters 20110819

Title: The synthesis of 2- and 3-aryl indoles and 1,3,4,5-tetrahydropyrano[4,3-b]indoles and their antibacterial and antifungal activity.

Journal: Bioorganic & medicinal chemistry letters 20090901

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

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SDS