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613-46-7,MFCD00016807
Catalog No.:AA003HOL

613-46-7 | 2-Naphthonitrile

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1g
98%
in stock  
$13.00   $9.00
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5g
98%
in stock  
$22.00   $15.00
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25g
98%
in stock  
$76.00   $54.00
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100g
98%
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$242.00   $170.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003HOL
Chemical Name:
2-Naphthonitrile
CAS Number:
613-46-7
Molecular Formula:
C11H7N
Molecular Weight:
153.1800
MDL Number:
MFCD00016807
SMILES:
N#Cc1ccc2c(c1)cccc2
NSC Number:
4169
Properties
Properties
 
BP:
306.5°C  
Form:
Solid  
MP:
63-68 °C  
Refractive Index:
1.6210 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
200  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
XLogP3:
3.2  

Upstream Synthesis Route

[1]ChemischeBerichte,1876,vol.9,p.1519

[1]JournalfuerPraktischeChemie(Leipzig),1891,vol.<2>43,p.427

[1]JournalofCarbohydrateChemistry,2011,vol.30,#7-9,p.559-574

[2]GreenChemistry,2013,vol.15,#11,p.3020-3026

[3]Patent:US2006/205728,2006,A1,.Locationinpatent:Page/Pagecolumn31

[4]JournalofOrganicChemistry,2015,vol.80,#14,p.7281-7287

[5]Synlett,2017,vol.28,#20,p.2855-2858

[1]GreenChemistry,2013,vol.15,#11,p.3020-3026

Downstream Synthesis Route

[1]Locationinpatent:experimentalpartLukas,RonaldJ.;Muresan,AnaZ.;Damaj,M.Imad;Blough,BruceE.;Huang,Xiaodong;Navarro,HernánA.;Mascarella,S.Wayne;Eaton,J.Brek;Marxer-Miller,SyndiaK.;Carroll,F.Ivy[JournalofMedicinalChemistry,2010,vol.53,#12,p.4731-4748]

[2]Haworth;Mavin;Sheldrick[JournaloftheChemicalSociety,1934,p.454,458]Hartung;Munch;Crossley[JournaloftheAmericanChemicalSociety,1935,vol.57,p.1091]

[3]Haworth;Mavin;Sheldrick[JournaloftheChemicalSociety,1934,p.454,458]Hartung;Munch;Crossley[JournaloftheAmericanChemicalSociety,1935,vol.57,p.1091]

[1]JournaloftheAmericanChemicalSociety,1929,vol.51,p.2278

[1]AngewandteChemie-InternationalEdition,2008,vol.47,p.3607-3609

[2]Synthesis,1980,p.243-244

[3]ChemistryLetters,2012,vol.41,p.633-635

[4]ChemicalCommunications,2009,p.3258-3260

[5]AppliedOrganometallicChemistry,2014,vol.28,p.900-907

[6]Catalysisscienceandtechnology,2015,vol.5,p.1606-1622

[7]TetrahedronLetters,2012,vol.53,p.2860-2863

[8]Chemistry-AEuropeanJournal,2017,vol.23,p.7761-7771

[9]CatalysisLetters,2018,vol.148,p.3378-3388

[10]EuropeanJournalofOrganicChemistry,2017,vol.2017,p.1870-1875

[11]NewJournalofChemistry,2018,vol.42,p.15221-15230

[12]Organometallics,2012,vol.31,p.3790-3797

[13]GreenChemistry,2014,vol.16,p.2136-2141

[14]GazzettaChimicaItaliana,1884,vol.14,p.122

[15]JournaloftheAmericanChemicalSociety,1917,vol.39,p.105

[16]JustusLiebigsAnnalenderChemie,1876,vol.180,p.305    ChemischeBerichte,1875,vol.8,p.1278

[17]AngewandteChemie-InternationalEdition,2012,vol.51,p.544-547

[18]ChemistryLetters,2012,vol.41,p.574-576

[19]SyntheticCommunications,2013,vol.43,p.2867-2875

[20]JournalofMolecularCatalysisA:Chemical,2015,vol.398,p.312-324

[21]Catalysisscienceandtechnology,2015,vol.5,p.3822-3828

[22]InorganicaChimicaActa,2016,vol.442,p.134-144

[1]Johansson,Henrik;Cailly,Thomas;Thomsen,AlexRojasBie;Braeuner-Osborne,Hans;Pedersen,DanielSejer[BeilsteinJournalofOrganicChemistry,2013,vol.9,p.1383-1387]

[2]Kamochi;Kudo[Tetrahedron,1992,vol.48,#21,p.4301-4312]

[3]Parker,David;Williams,J.A.Gareth[JournaloftheChemicalSociety.PerkintransactionsII,1995,#7,p.1305-1314]

[4]Mullangi,Dinesh;Chakraborty,Debanjan;Pradeep,Anu;Koshti,Vijay;Vinod,ChathakudathP.;Panja,Soumendranath;Nair,Sunil;Vaidhyanathan,Ramanathan[Small,2018,vol.14,#37]

[5]Schneekönig,Jacob;Tannert,Bianca;Hornke,Helen;Beller,Matthias;Junge,Kathrin[Catalysisscienceandtechnology,2019,vol.9,#8,p.1779-1783]

[6]Cody,WayneL.;Holsworth,DanielD.;Powell,NoelA.;Jalaie,Mehran;Zhang,Erli;Wang,Wei;Samas,Brian;Bryant,John;Ostroski,Robert;Ryan,MichaelJ.;Edmunds,JeremyJ.[BioorganicandMedicinalChemistry,2005,vol.13,#1,p.59-68]

[7]CurrentPatentAssignee:PFIZERINC-US2004/204455,2004,A1Locationinpatent:Page/Pagecolumn17

[8]Anitha,Panneerselvam;Viswanathamurthi,Periasamy;Kesavan,Devarayan;Butcher,RayJay[JournalofCoordinationChemistry,2015,vol.68,#2,p.321-334]

[9]Sutter,Marc;Pehlivan,Leyla;Lafon,Romain;Dayoub,Wissam;Raoul,Yann;Metay,Estelle;Lemaire,Marc[GreenChemistry,2013,vol.15,#11,p.3020-3026]

[10]Dahn;Zoller;Solms[HelveticaChimicaActa,1954,vol.37,p.565,572]

[11]Dahn;Zoller;Solms[HelveticaChimicaActa,1954,vol.37,p.565,572]

[12]Bressi;Verlinde;Aronov;Shaw;Shin;Nguyen;Suresh;Buckner;vanVoorhis;Kuntz;Hol;Gelb[JournalofMedicinalChemistry,2001,vol.44,#13,p.2080-2093]

[13]Bamberger;Boekmann[ChemischeBerichte,1887,vol.20,p.1118]

[14]CurrentPatentAssignee:SumitomoChemical(w/oDongwooFine-Chem);SUMITOMOCHEMICALCOMPANYLIMITED-EP1577290,2005,A1Locationinpatent:Page/Pagecolumn101

[15]CurrentPatentAssignee:SumitomoChemical(w/oDongwooFine-Chem);SUMITOMOCHEMICALCOMPANYLIMITED-JP2005/314352,2005,ALocationinpatent:Page/Pagecolumn55-56

[16]CurrentPatentAssignee:SUMITOMOCHEMICALCOMPANYLIMITED;SumitomoChemical(w/oDongwooFine-Chem)-EP1609360,2005,A1Locationinpatent:Page/Pagecolumn19

[17]Chakraborty,Subrata;Leitus,Gregory;Milstein,David[ChemicalCommunications,2016,vol.52,#9,p.1812-1815]

[18]Cai,Wenqing;Wu,Jingwei;Liu,Wei;Xie,Yafei;Liu,Yuqiang;Zhang,Shuo;Xu,Weiren;Tang,Lida;Wang,Jianwu;Zhao,Guilong[Molecules,2018,vol.23,#2]

[19]Zhang,Yangmin;Yang,Hanmin;Chi,Quan;Zhang,Zehui[ChemSusChem,2019,vol.12,#6,p.1246-1255]

[20]Ganguli,Kasturi;Mandal,Adarsha;Sarkar,Bidisha;Kundu,Sabuj[Tetrahedron,2020,vol.76,#37]

[21]Striegler,Susanne;Orizu,Ifedi[CarbohydrateResearch,2022,vol.513]

[1]SyntheticCommunications,1997,vol.27,p.2393-2402

[2]Heterocycles,2018,vol.96,p.509-517

[3]RSCAdvances,2018,vol.8,p.170-175

[4]AmericanJournalofPharmacologyandToxicology,2019,vol.14,p.27-37

[5]JustusLiebigsAnnalenderChemie,1923,vol.431,p.213    ChemischesZentralblatt,1923,vol.94,p.403

[6]ChemischeBerichte,1887,vol.20,p.1118

[7]Synlett,2010,p.2861-2866

Literature

Title: Efficient and selective photodimerization of 2-naphthalenecarbonitrile mediated by cucurbit[8]uril in an aqueous solution.

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20110901

Title: Hydrogen-bonding directed, regioselective photocycloaddition reactions of cyanonaphthalenes with furanmethanols.

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20110901

Title: Synthesis and anti-HIV activity of 2-naphthyl substituted DAPY analogues as non-nucleoside reverse transcriptase inhibitors.

Journal: Bioorganic & medicinal chemistry 20100701

Title: Mechanisms of formation of nitrogen-containing polycyclic aromatic compounds in low-temperature environments of planetary atmospheres: a theoretical study.

Journal: Faraday discussions 20100101

Title: Formation of cubane-like photodimers from 2-naphthalenecarbonitrile.

Journal: The Journal of organic chemistry 20080919

Title: Residues distant from the active site influence protein-tyrosine phosphatase 1B inhibitor binding.

Journal: The Journal of biological chemistry 20060224

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