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22110-53-8,MFCD02258889
Catalog No.:AA00BD1B

22110-53-8 | 1-Adamantyl isocyanide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97% GC
in stock  
$162.00   $113.00
- +
5g
>97.0%(GC)
in stock  
$603.00   $422.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00BD1B
Chemical Name:
1-Adamantyl isocyanide
CAS Number:
22110-53-8
Molecular Formula:
C11H15N
Molecular Weight:
161.2435
MDL Number:
MFCD02258889
SMILES:
[C-]#[N+]C12CC3CC(C2)CC(C1)C3
Properties
Computed Properties
 
Complexity:
216  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.6  

Downstream Synthesis Route

[1]Ahmadian-Moghaddam,Maryam;Dömling,Alexander;Patil,Pravin[GreenChemistry,2020,vol.22,#20,p.6902-6911]

[2]Škoch,Karel;Císařová,Ivana;Štěpnička,Petr[Chemistry-AEuropeanJournal,2018,vol.24,#52,p.13788-13791]

[3]Locationinpatent:schemeortableGravestock,David;Rousseau,AmandaL.;Lourens,AnnaC.U.;Hoppe,HeinrichC.;Nkabinde,LindiweA.;Bode,MoiraL.[TetrahedronLetters,2012,vol.53,#26,p.3225-3229]

[4]Waibel;Nickisch;Möhl;Seim;Meier[GreenChemistry,2020,vol.22,#3,p.933-941]

[5]Minozzi,Matteo;Nanni,Daniele;Walton,JohnC.[OrganicLetters,2003,vol.5,#6,p.901-904]

[6]Barton,DerekH.R.;Jang,DooOk;Jaszberenyi,JosephCs.[Tetrahedron,1993,vol.49,#33,p.7193-7214]

[7]Locationinpatent:experimentalpartHashmi,A.StephenK.;Yu,Yang;Rominger,Frank[Organometallics,2012,vol.31,#3,p.895-904]

[8]Jia,Shuanglong;Su,Shikuan;Li,Chunju;Jia,Xueshun;Li,Jian[OrganicLetters,2014,vol.16,#21,p.5604-5607]

[9]Shaabani;Neochoritis;Twarda-Clapa;Musielak;Holak;Dömling[MedChemComm,2017,vol.8,#5,p.1046-1052]

[10]Zhang,Fengcai;Sang,Xinpeng;Zhou,Yuqiao;Cao,Weidi;Feng,Xiaoming[OrganicLetters,2022,vol.24,#7,p.1513-1517]

[1]Kitano;Chiba;Tada[Synthesis,2001,#3,p.437-443]

[2]Fang,Yi;Zhu,Zheng-Lin;Xu,Pei;Wang,Shun-Yi;Ji,Shun-Jun[GreenChemistry,2017,vol.19,#7,p.1613-1618]

[3]Jiang,Tian;Gu,Zheng-Yang;Yin,Ling;Wang,Shun-Yi;Ji,Shun-Jun[JournalofOrganicChemistry,2017,vol.82,#15,p.7913-7919]

[4]Liu,Huan;Fang,Yi;Wang,Shun-Yi;Ji,Shun-Jun[OrganicLetters,2018,vol.20,#4,p.930-933]

[5]Li,Qiao;Cai,Yun;Jin,Hongwei;Liu,Yunkui;Zhou,Bingwei[TetrahedronLetters,2020,vol.61,#51]

[6]Locationinpatent:schemeortableOkada,Iku;Kitano,Yoshikazu[Synthesis,2011,#24,p.3997-4002]

[1]Ley,StevenV;Taylor,StephenJ[Bioorganicandmedicinalchemistryletters,2002,vol.12,#14,p.1813-1816]

22110-53-8    123-11-5    88284-48-4   
N-3-(4-methoxyphenyl)-(3H)-isobenzofuran-1-ylidene-1-adamantylamine 

[1]Yoshida,Hiroto;Fukushima,Hiroyuki;Ohshita,Joji;Kunai,Atsutaka[AngewandteChemie-InternationalEdition,2004,vol.43,#30,p.3935-3938]

22110-53-8    250665-62-4   
N-(1-adamantyl)-1,1-1,1,4,4-tetrakis(trimethylsilyl)butane-1,4-diylsilaketenimine 

[1]Abe,Takashi;Iwamoto,Takeaki;Kabuto,Chizuko;Kira,Mitsuo[JournaloftheAmericanChemicalSociety,2006,vol.128,#13,p.4228-4229]

Literature

Title: Stability-enhanced hydrogen-evolving dirhodium photocatalysts through ligand modification.

Journal: Chemical communications (Cambridge, England) 20121004

Title: Oxygen reduction reactions of monometallic rhodium hydride complexes.

Journal: Inorganic chemistry 20120702

Title: Synthesis, structure, and bonding of stable dialkylsilaketenimines.

Journal: Journal of the American Chemical Society 20060405

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Tags:22110-53-8 Molecular Formula|22110-53-8 MDL|22110-53-8 SMILES|22110-53-8 1-Adamantyl isocyanide
Catalog No.: AA00BD1B
22110-53-8,MFCD02258889
22110-53-8 | 1-Adamantyl isocyanide
Pack Size： 1g
Purity： 97% GC
in stock
$162.00 $113.00
Pack Size： 5g
Purity： >97.0%(GC)
in stock
$603.00 $422.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00BD1B
Chemical Name: 1-Adamantyl isocyanide
CAS Number: 22110-53-8
Molecular Formula: C11H15N
Molecular Weight: 161.2435
MDL Number: MFCD02258889
SMILES: [C-]#[N+]C12CC3CC(C2)CC(C1)C3
Properties
Complexity: 216  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.6  
Downstream Synthesis Route
3405-48-9    22110-53-8 

[1]Ahmadian-Moghaddam,Maryam;Dömling,Alexander;Patil,Pravin[GreenChemistry,2020,vol.22,#20,p.6902-6911]

[2]Škoch,Karel;Císařová,Ivana;Štěpnička,Petr[Chemistry-AEuropeanJournal,2018,vol.24,#52,p.13788-13791]

[3]Locationinpatent:schemeortableGravestock,David;Rousseau,AmandaL.;Lourens,AnnaC.U.;Hoppe,HeinrichC.;Nkabinde,LindiweA.;Bode,MoiraL.[TetrahedronLetters,2012,vol.53,#26,p.3225-3229]

[4]Waibel;Nickisch;Möhl;Seim;Meier[GreenChemistry,2020,vol.22,#3,p.933-941]

[5]Minozzi,Matteo;Nanni,Daniele;Walton,JohnC.[OrganicLetters,2003,vol.5,#6,p.901-904]

[6]Barton,DerekH.R.;Jang,DooOk;Jaszberenyi,JosephCs.[Tetrahedron,1993,vol.49,#33,p.7193-7214]

[7]Locationinpatent:experimentalpartHashmi,A.StephenK.;Yu,Yang;Rominger,Frank[Organometallics,2012,vol.31,#3,p.895-904]

[8]Jia,Shuanglong;Su,Shikuan;Li,Chunju;Jia,Xueshun;Li,Jian[OrganicLetters,2014,vol.16,#21,p.5604-5607]

[9]Shaabani;Neochoritis;Twarda-Clapa;Musielak;Holak;Dömling[MedChemComm,2017,vol.8,#5,p.1046-1052]

[10]Zhang,Fengcai;Sang,Xinpeng;Zhou,Yuqiao;Cao,Weidi;Feng,Xiaoming[OrganicLetters,2022,vol.24,#7,p.1513-1517]

7677-24-9    768-95-6    22110-53-8 

[1]Kitano;Chiba;Tada[Synthesis,2001,#3,p.437-443]

[2]Fang,Yi;Zhu,Zheng-Lin;Xu,Pei;Wang,Shun-Yi;Ji,Shun-Jun[GreenChemistry,2017,vol.19,#7,p.1613-1618]

[3]Jiang,Tian;Gu,Zheng-Yang;Yin,Ling;Wang,Shun-Yi;Ji,Shun-Jun[JournalofOrganicChemistry,2017,vol.82,#15,p.7913-7919]

[4]Liu,Huan;Fang,Yi;Wang,Shun-Yi;Ji,Shun-Jun[OrganicLetters,2018,vol.20,#4,p.930-933]

[5]Li,Qiao;Cai,Yun;Jin,Hongwei;Liu,Yunkui;Zhou,Bingwei[TetrahedronLetters,2020,vol.61,#51]

[6]Locationinpatent:schemeortableOkada,Iku;Kitano,Yoshikazu[Synthesis,2011,#24,p.3997-4002]

4411-26-1    22110-53-8 

[1]Ley,StevenV;Taylor,StephenJ[Bioorganicandmedicinalchemistryletters,2002,vol.12,#14,p.1813-1816]

22110-53-8    123-11-5    88284-48-4   
N-3-(4-methoxyphenyl)-(3H)-isobenzofuran-1-ylidene-1-adamantylamine 

[1]Yoshida,Hiroto;Fukushima,Hiroyuki;Ohshita,Joji;Kunai,Atsutaka[AngewandteChemie-InternationalEdition,2004,vol.43,#30,p.3935-3938]

22110-53-8    250665-62-4   
N-(1-adamantyl)-1,1-1,1,4,4-tetrakis(trimethylsilyl)butane-1,4-diylsilaketenimine 

[1]Abe,Takashi;Iwamoto,Takeaki;Kabuto,Chizuko;Kira,Mitsuo[JournaloftheAmericanChemicalSociety,2006,vol.128,#13,p.4228-4229]

Literature fold

Title: Stability-enhanced hydrogen-evolving dirhodium photocatalysts through ligand modification.

Journal: Chemical communications (Cambridge, England)20121004

Title: Oxygen reduction reactions of monometallic rhodium hydride complexes.

Journal: Inorganic chemistry20120702

Title: Synthesis, structure, and bonding of stable dialkylsilaketenimines.

Journal: Journal of the American Chemical Society20060405

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