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2377-81-3,MFCD00013290
Catalog No.:AA003FIN

2377-81-3 | Tetrafluoroisophthalonitrile

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250mg
98%
in stock  
$7.00   $5.00
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1g
98%
in stock  
$13.00   $9.00
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5g
98%
in stock  
$42.00   $29.00
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10g
98%
in stock  
$82.00   $57.00
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25g
98%
in stock  
$175.00   $123.00
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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:
AA003FIN
Chemical Name:
Tetrafluoroisophthalonitrile
CAS Number:
2377-81-3
Molecular Formula:
C8F4N2
Molecular Weight:
200.0926
MDL Number:
MFCD00013290
SMILES:
N#Cc1c(F)c(C#N)c(c(c1F)F)F
Properties
Properties
 
BP:
212.5°C at 760 mmHg  
Form:
Solid  
MP:
78-79°C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
284  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
6  
XLogP3:
1.8  

Downstream Synthesis Route
86-74-8   
tetrafluoroisophthalonitrile 
  1416881-52-1 

[1]AngewandteChemie-InternationalEdition,2017,vol.56,p.1500-1505    Angew.Chem.,2017,vol.129,p.1522-1527,6

[2]JournaloftheAmericanChemicalSociety,2017,vol.139,p.9799-9802

[3]AngewandteChemie-InternationalEdition,2020,vol.59,p.5172-5177    Angew.Chem.,2020,vol.132,p.5210-5215,6

[4]OrganicLetters,2018,vol.20,p.5533-5536

[5]ChineseChemicalLetters,2019

[6]Chemistry-AEuropeanJournal,2020

[7]JournalofOrganicChemistry,2020,vol.85,p.3426-3439

[8]Nature,2012,vol.492,p.234-238

[9]OrganicSyntheses,2019,vol.96,p.455-473

[10]AngewandteChemie-InternationalEdition,2018,vol.57,p.11278-11282    Angew.Chem.,2018,vol.130,p.11448-11452,5

[11]JournalofMaterialsChemistryA,2020,vol.8,p.3708-3716

[12]AngewandteChemie-InternationalEdition,2019,vol.58,p.1789-1793    Angew.Chem.,2019,vol.131,p.1803-1807,5

[13]AngewandteChemie-InternationalEdition,2019,vol.58,p.9199-9203    Angew.Chem.,2019,vol.131,p.9297-9301,5

[14]AdvancedSynthesisandCatalysis,2020,vol.362,p.2254-2259

[15]ChemicalScience,2018,vol.9,p.5883-5889

[16]AngewandteChemie-InternationalEdition,2019,vol.58,p.8182-8186    Angew.Chem.,2019,vol.131,p.8266-8270,5

[17]OrganicLetters,2019,vol.21,p.8957-8961

[18]ChemicalCommunications,2016,vol.52,p.9877-9880

[19]ChemicalCommunications,2018,vol.54,p.9337-9340

[20]ChemicalCommunications,2019,vol.55,p.466-469

[21]JournalofOrganicChemistry,2015,vol.80,p.9126-9131

[22]Advancedsynthesisandcatalysis,2020

[23]ChemicalCommunications,2018,vol.54,p.5606-5609

[24]Patent:US9502668,2016,B2.Locationinpatent:Page/Pagecolumn126;127

[25]Patent:CN107382910,2017,A.Locationinpatent:Paragraph0015;0016

[26]Patent:US10323180,2019,B2.Locationinpatent:Page/Pagecolumn41;42

[27]ChemicalCommunications,2020,vol.56,p.4240-4243

5599-71-3   
tetrafluoroisophthalonitrile 
 
(2r,4s,5r)-2,4,5,6-Tetrakis(3,6-dichloro-9H-carbazol-9-yl)isophthalonitrile 

[1]LeVaillant,Franck;Garreau,Marion;Nicolai,Stefano;Gryn'Ova,Ganna;Corminboeuf,Clemence;Waser,Jerome[ChemicalScience,2018,vol.9,#27,p.5883-5889]

[2]Garreau,Marion;LeVaillant,Franck;Waser,Jerome[AngewandteChemie-InternationalEdition,2019,vol.58,#24,p.8182-8186][Angew.Chem.,2019,vol.131,p.8266-8270,5]

[3]Amos,StephanieG.E.;Cavalli,Diana;LeVaillant,Franck;Waser,Jerome[AngewandteChemie-InternationalEdition,2021,vol.60,#44,p.23827-23834][Angew.Chem.,2021,vol.133,#44,p.24020-24027]

[4]Borrel,Julien;Waser,Jerome[OrganicLetters,2022,vol.24,#1,p.142-146]

[5]Kretzschmar,Andreas;Patze,Christian;Schwaebel,S.Thimon;Bunz,UweH.F.[JournalofOrganicChemistry,2015,vol.80,#18,p.9126-9131]

[6]Wiles,RebeccaJ.;Phelan,JamesP.;Molander,GaryA.[ChemicalCommunications,2019,vol.55,#53,p.7599-7602]

[7]Liu,Yan;Chen,Xiao-Lan;Li,Xiao-Yun;Zhu,Shan-Shan;Li,Shi-Jun;Song,Yan;Qu,Ling-Bo;Yu,Bing[JournaloftheAmericanChemicalSociety,2021,vol.143,#2,p.964-972]

[1]Miyashita,Yasuhiro;Park,InSeob;Tanaka,Katsunori;Yang,Minlang;Yasuda,Takuma[AngewandteChemie-InternationalEdition,2020,vol.59,#33,p.13955-13961][Angew.Chem.,2020,vol.132,#33,p.14059-14065,7]

[2]Garreau,Marion;LeVaillant,Franck;Waser,Jerome[AngewandteChemie-InternationalEdition,2019,vol.58,#24,p.8182-8186][Angew.Chem.,2019,vol.131,p.8266-8270,5]

[3]Leitch,JamieA.;Smallman,HarryR.;Browne,DuncanL.[JournalofOrganicChemistry,2021,vol.86,#20,p.14095-14101]

[4]Ishimatsu,Ryoichi;Edura,Tomohiko;Adachi,Chihaya;Nakano,Koji;Imato,Toshihiko[Chemistry-AEuropeanJournal,2016,vol.22,#14,p.4889-4898]

[5]Liu,Yan;Chen,Xiao-Lan;Li,Xiao-Yun;Zhu,Shan-Shan;Li,Shi-Jun;Song,Yan;Qu,Ling-Bo;Yu,Bing[JournaloftheAmericanChemicalSociety,2021,vol.143,#2,p.964-972]

56525-79-2   
tetrafluoroisophthalonitrile 
 
1,2,3,5-tetrakis(3,6-diphenylcarbazol-9-yl)-4,6-dicyanobenzene 

[1]Chemistry-AEuropeanJournal,2016,vol.22,p.4889-4898

[1]Garreau,Marion;LeVaillant,Franck;Waser,Jerome[AngewandteChemie-InternationalEdition,2019,vol.58,#24,p.8182-8186][Angew.Chem.,2019,vol.131,p.8266-8270,5]

[2]Speckmeier,Elisabeth;Fischer,TillmannG.;Zeitler,Kirsten[JournaloftheAmericanChemicalSociety,2018,vol.140,#45,p.15353-15365]

[3]Liu,Yan;Chen,Xiao-Lan;Li,Xiao-Yun;Zhu,Shan-Shan;Li,Shi-Jun;Song,Yan;Qu,Ling-Bo;Yu,Bing[JournaloftheAmericanChemicalSociety,2021,vol.143,#2,p.964-972]

Literature

Title: Synthesis and antimicrobial activity of polyhalo isophthalonitrile derivatives.

Journal: Bioorganic & medicinal chemistry letters 20130415

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