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139152-08-2,MFCD00191408
Catalog No.:AA001ABR

139152-08-2 | 4,5-Dichlorophthalonitrile

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1g
95%
in stock  
$42.00   $30.00
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5g
95%
in stock  
$126.00   $89.00
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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:
AA001ABR
Chemical Name:
4,5-Dichlorophthalonitrile
CAS Number:
139152-08-2
Molecular Formula:
C8H2Cl2N2
Molecular Weight:
197.0209
MDL Number:
MFCD00191408
SMILES:
N#Cc1cc(Cl)c(cc1C#N)Cl
Properties
Computed Properties
 
Complexity:
231  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
XLogP3:
2.6  

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,2008,vol.51,p.502-511

[2]Synthesis,1993,p.194-196

[3]JournalofPhotochemistryandPhotobiologyA:Chemistry,2011,vol.219,p.217-227

[4]RSCAdvances,2016,vol.6,p.40442-40449

[1]Patent:EP638614,1995,A1

[2]Synthesis,1993,p.194-196

[3]ChemistryLetters,2010,vol.39,p.1194-1196

[4]AngewandteChemie-InternationalEdition,2015,vol.54,p.15152-15155    Angew.Chem.,2015,vol.127,p.15367-15370,4

[5]Patent:KR2018/17774,2018,A.Locationinpatent:Paragraph0083;0091-0092

[1]TetrahedronLetters,2009,vol.50,p.6882-6885

[2]RussianJournalofGeneralChemistry,2016,vol.86,p.854-858    Zh.Obshch.Khim.,2016,vol.86,p.667-671,5

[3]RussianJournalofGeneralChemistry,2018,vol.88,p.1148-1153    Zh.Obshch.Khim.,2018,vol.88,p.968-973,6

[4]RSCAdvances,2015,vol.5,p.13828-13839

[5]JournaloftheChemicalSociety.PerkinTransactions1(2001),2002,vol.2,p.91-96

[6]Synthesis,1993,p.194-196

[7]JournalofCatalysis,2019,vol.373,p.222-227

[8]Synthesis,2005,p.1141-1147

[9]Patent:US2004/254215,2004,A1.Locationinpatent:Page80-81

[10]InorganicaChimicaActa,2010,vol.363,p.3945-3950

[1]JournalofOrganicChemistry,2010,vol.75,p.7893-7896

[2]JournaloftheAmericanChemicalSociety,1998,vol.120,p.12808-12817

[3]JournalofMaterialsChemistry,2000,vol.10,p.1083-1090

[4]Synthesis,2005,p.1141-1147

[5]JournalofMaterialsChemistry,2001,vol.11,p.321-331

[6]JournalofMolecularStructure,2010,vol.973,p.96-103

[7]JournalofMaterialsChemistry,2010,vol.20,p.1292-1303

[8]NewJournalofChemistry,2012,vol.36,p.1665-1672

[9]ChemicalScience,2013,vol.4,p.1338-1344

[10]JournalofPorphyrinsandPhthalocyanines,2016,vol.20,p.1122-1133

143-10-2    139152-08-2   
4,5-bis(decylthio)phthalonitrile 

[1]Locationinpatent:experimentalpartMayukh,Mayank;Sema,ClarissaM.;Roberts,JessicaM.;McGrath,DominicV.[JournalofOrganicChemistry,2010,vol.75,#22,p.7893-7896]

[2]Locationinpatent:experimentalpartCoates,Megan;Antunes,Edith;Nyokong,Tebello[JournalofPorphyrinsandPhthalocyanines,2010,vol.14,#7,p.568-581]

[3]Kang,SeokHo;Kang,Yoon-Sok;Zin,Wang-Cheol;Olbrechts,Geert;Wostyn,Kurt;Clays,Koen;Persoons,Andre;Kim,Kimoon[ChemicalCommunications,1999,#17,p.1661-1662]

[4]Ban,Kazue;Kaoru,Nishizawa;Ohta,Kazuchika;Shirai,Hirofusa[JournalofMaterialsChemistry,2000,vol.10,#5,p.1083-1090]

[5]Ban;Nishizawa;Ohta;VandeCraats;Warman;Yamamoto;Shirai[JournalofMaterialsChemistry,2001,vol.11,#2,p.321-331]

Literature

Title: 4,5-Diphen-oxy-benzene-1,2-dicarbo-nitrile.

Journal: Acta crystallographica. Section E, Structure reports online 20120301

Title: 4,5-Bis(2,4-di-tert-butyl-phen-oxy)phthalonitrile.

Journal: Acta crystallographica. Section E, Structure reports online 20110301

Title: Preparation and in vitro photodynamic activity of amphiphilic zinc(II) phthalocyanines substituted with 2-(dimethylamino)ethylthio moieties and their N-alkylated derivatives.

Journal: Bioorganic & medicinal chemistry 20100401

Title: Synthesis, characterization and nonlinear absorption of novel octakis-POSS substituted metallophthalocyanines and strong optical limiting property of CuPc.

Journal: Dalton transactions (Cambridge, England : 2003) 20080514

Title: Synthesis and photophysical properties of tetra- and octasubstituted phosphorous oxide triazatetrabenzcorrole photosensitizers.

Journal: Metal-based drugs 20080101

Title: Tetrapyrrole derivatives substituted with ferrocenylethynyl moieties. synthesis and electrochemical studies.

Journal: The Journal of organic chemistry 20010309

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