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2132-62-9,MFCD00025844
Catalog No.:AA007QQA

2132-62-9 | 1,2-Bis(4-methoxyphenyl)ethyne

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250mg
98%
in stock  
$112.00   $78.00
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1g
98%
in stock  
$261.00   $183.00
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5g
98%
in stock  
$809.00   $567.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA007QQA
Chemical Name:
1,2-Bis(4-methoxyphenyl)ethyne
CAS Number:
2132-62-9
Molecular Formula:
C16H14O2
Molecular Weight:
238.2812
MDL Number:
MFCD00025844
SMILES:
COc1ccc(cc1)C#Cc1ccc(cc1)OC
Properties
Computed Properties
 
Complexity:
268  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
4  
XLogP3:
3.9  

Downstream Synthesis Route

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[2]JournalofOrganicChemistry,2011,vol.76,p.724-727

[3]AngewandteChemie-InternationalEdition,1999,vol.38,p.3483-3486

[4]JournalofOrganometallicChemistry,1971,vol.26,p.407-415

[5]JournalofMaterialsChemistry,2008,vol.18,p.1903-1910

[6]DaltonTransactions,2011,vol.40,p.10047-10054

[1]JournalofMedicinalChemistry,1989,vol.32,p.1814-1820

[1]Patent:WO2008/157745,2008,A1.Locationinpatent:Page/Pagecolumn19

[2]JournalofOrganicChemistry,1982,vol.47,p.4941-4947

[3]JournaloftheChemicalSociety,DaltonTransactions,2001,p.1401-1414

[4]TetrahedronLetters,1994,vol.35,p.857-860

[5]Patent:US5830920,1998,A

[1]JournalofOrganicChemistry,2018,vol.83,p.4703-4711

[2]RussianJournalofOrganicChemistry,1995,vol.31,p.1503-1506    ZhurnalOrganicheskoiKhimii,1995,vol.31,p.1675-1678

[3]TetrahedronLetters,2015,vol.56,p.1517-1519

[4]JournalofOrganicChemistry,2016,vol.81,p.7256-7261

[5]OrganicLetters,2020,vol.22,p.4190-4195

[6]AppliedOrganometallicChemistry,2017,vol.31

[7]AdvancedSynthesisandCatalysis,2010,vol.352,p.1630-1634

[8]EuropeanJournalofOrganicChemistry,2011,p.3361-3367

[9]TetrahedronLetters,2019,vol.60,p.843-846

[10]JournalofOrganicChemistryUSSR(EnglishTranslation),1987,vol.23,p.1967-1969    ZhurnalOrganicheskoiKhimii,1987,vol.23,p.2225-2227

[11]AdvancedSynthesisandCatalysis,2019,vol.361,p.1846-1858

[12]Patent:CN104892377,2018,B.Locationinpatent:Paragraph0059-0062

[13]OrganicLetters,2019,vol.21,p.2514-2517

[14]OrganicLetters,2012,vol.14,p.4594-4597

[15]Chemistry-AnAsianJournal,2019,vol.14,p.4774-4779

[1]AdvancedSynthesisandCatalysis,2006,vol.348,p.1874-1882

[2]AdvancedSynthesisandCatalysis,2018,vol.360,p.313-321

[3]CatalysisCommunications,2014,vol.47,p.40-44

[4]Tetrahedron,2001,vol.57,p.7839-7844

[5]TetrahedronLetters,2004,vol.45,p.4337-4340

[6]Tetrahedron,2010,vol.66,p.9415-9420

[7]JournaloftheAmericanChemicalSociety,2010,vol.132,p.9585-9587

[8]AdvancedSynthesisandCatalysis,2015,vol.357,p.89-99

[9]Chemistry-AEuropeanJournal,2011,vol.17,p.3942-3948

[10]EuropeanJournalofOrganicChemistry,2017,vol.2017,p.4405-4413

[11]ChemicalCommunications,2018,vol.54,p.10598-10601

[12]AdvancedSynthesisandCatalysis,2019,vol.361,p.683-689

Literature

Title: Borylene-based direct functionalization of organic substrates: synthesis, characterization, and photophysical properties of novel pi-conjugated borirenes.

Journal: Journal of the American Chemical Society 20090701

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