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56108-12-4,MFCD00017139
Catalog No.:AA003LYU

56108-12-4 | 4-(tert-Butyl)benzamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$14.00   $10.00
- +
5g
98%
in stock  
$37.00   $26.00
- +
25g
97%
in stock  
$143.00   $100.00
- +
100g
97%
in stock  
$400.00   $280.00
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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:
AA003LYU
Chemical Name:
4-(tert-Butyl)benzamide
CAS Number:
56108-12-4
Molecular Formula:
C11H15NO
Molecular Weight:
177.2429
MDL Number:
MFCD00017139
SMILES:
NC(=O)c1ccc(cc1)C(C)(C)C
Properties
Properties
 
BP:
293.2°C at 760 mmHg  
Form:
Solid  
MP:
170 °C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
185  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
2.5  

Downstream Synthesis Route

[1]Locationinpatent:experimentalpartEnthaler,Stephan;Weidauer,Maik[CatalysisLetters,2011,vol.141,#8,p.1079-1085]

[2]Enthaler,Stephan[Chemistry-AEuropeanJournal,2011,vol.17,#34,p.9316-9319]

[3]Enthaler,Stephan[EuropeanJournalofOrganicChemistry,2011,#25,p.4760-4763]

[4]Locationinpatent:experimentalpartEnthaler,Stephan;Inoue,Shigeyoshi[Chemistry-AnAsianJournal,2012,vol.7,#1,p.169-175]

[5]Zhou,Shaolin;Junge,Kathrin;Addis,Daniele;Das,Shoubhik;Beller,Matthias[OrganicLetters,2009,vol.11,#11,p.2461-2464]

[6]Ruan,Shixiang;Ruan,Jiancheng;Chen,Xinzhi;Zhou,Shaodong[Molecularcatalysis,2021,vol.499]

[7]Zhou,Shaolin;Addis,Daniele;Das,Shoubhik;Junge,Kathrin;Beller,Matthias[ChemicalCommunications,2009,#32,p.4883-4885]

[8]Keita,Massaba;Vandamme,Mathilde;Paquin,Jean-François[Synthesis,2015,vol.47,#23,p.3758-3766]

[9]CurrentPatentAssignee:ZHEJIANGUNIVERSITYOFTECHNOLOGY-CN112961079,2021,ALocationinpatent:Paragraph0105-0107

[10]Yokoyama,Masataka;Yoshida,Sayaka;Imamoto,Tsuneo[Synthesis,1982,#7,p.591-592]

[11]Brown[JournaloftheAmericanChemicalSociety,1959,vol.81,p.3232,3233]

[12]Ruechardt,C.;Eichler,S.[ChemischeBerichte,1962,vol.95,p.1921-1942]

[13]CurrentPatentAssignee:ZHEJIANGUNIVERSITY-CN112028726,2020,ALocationinpatent:Paragraph0033-0054;0061-0065

[1]Ruechardt,C.;Eichler,S.[ChemischeBerichte,1962,vol.95,p.1921-1942]

[2]Mohammad,Haroon;Mayhoub,AbdelrahmanS.;Ghafoor,Adil;Soofi,Muhammad;Alajlouni,RubaA.;Cushman,Mark;Seleem,MohamedN.[JournalofMedicinalChemistry,2014,vol.57,#4,p.1609-1615]

[3]Wu,Youzhi;Sun,Peng;Zhang,Kaifan;Yang,Tie;Yao,Hequan;Lin,Aijun[JournalofOrganicChemistry,2016,vol.81,#5,p.2166-2173]

[4]Lei,Peng;Xu,Yan;Du,Juan;Yang,Xin-Ling;Yuan,Hui-Zhu;Xu,Gao-Fei;Ling,Yun[BioorganicandMedicinalChemistryLetters,2016,vol.26,#10,p.2544-2546]

[5]CurrentPatentAssignee:WUHANUNIVERSITY-CN113582969,2021,ALocationinpatent:Paragraph0053-0056

[1]Weikert;BinghamJr.;Emanuel;Fraser-Smith;Loughhead;Nelson;Poulton[JournalofMedicinalChemistry,1991,vol.34,#5,p.1630-1633]

[2]CurrentPatentAssignee:UNIVERSITYOFSTANDREWS;UNIVERSITYOFDUNDEE-WO2008/29096,2008,A2Locationinpatent:Page/Pagecolumn48

[3]Lei,Peng;Xu,Yan;Du,Juan;Yang,Xin-Ling;Yuan,Hui-Zhu;Xu,Gao-Fei;Ling,Yun[BioorganicandMedicinalChemistryLetters,2016,vol.26,#10,p.2544-2546]

[4]CurrentPatentAssignee:WUHANUNIVERSITY-CN113582969,2021,ALocationinpatent:Paragraph0053-0056

[1]Locationinpatent:schemeortableWu,Xiao-Feng;Neumann,Helfried;Beller,Matthias[Chemistry-AEuropeanJournal,2010,vol.16,#32,p.9750-9753]

[2]Locationinpatent:experimentalpartWu,Xiao-Feng;Neumann,Helfried;Beller,Matthias[Chemistry-AnAsianJournal,2010,vol.5,#10,p.2168-2172]

[3]Schnyder;Beller;Mehltretter;Nsenda;Studer;Indolese[JournalofOrganicChemistry,2001,vol.66,#12,p.4311-4315]

[1]Sierra,MichaelL.;Beneton,Véronique;Boullay,Anne-Bénédict;Boyer,Thierry;Brewster,AndrewG.;Donche,Frédéric;Forest,Marie-Claire;Fouchet,Marie-Hélène;Gellibert,FrançoiseJ.;Grillot,DidierA.;Lambert,MillardH.;Laroze,Alain;LeGrumelec,Christelle;Linget,JeanMichel;Montana,ValerieG.;Nguyen,Van-Loc;Nicodème,Edwige;Patel,Vipul;Penfornis,Annie;Pineau,Olivier;Pohin,Danig;Potvain,Florent;Poulain,Géraldine;Ruault,CécileBertho;Saunders,Michael;Toum,Jérôme;Xu,H.Eric;Xu,RobertX.;Pianetti,PascalM.[JournalofMedicinalChemistry,2007,vol.50,#4,p.685-695]

[2]Nambo,Masakazu;Segawa,Yasutomo;Itami,Kenichiro[JournaloftheAmericanChemicalSociety,2011,vol.133,#8,p.2402-2405]

[3]Mohammad,Haroon;Mayhoub,AbdelrahmanS.;Ghafoor,Adil;Soofi,Muhammad;Alajlouni,RubaA.;Cushman,Mark;Seleem,MohamedN.[JournalofMedicinalChemistry,2014,vol.57,#4,p.1609-1615]

[4]Peng,Xiangjun;Qin,Feng;Xu,Mengyue;Zhu,Shaojie;Pan,Yingming;Tang,Haitao;Meng,Xiujin;Wang,Hengshan[OrganicandBiomolecularChemistry,2019,vol.17,#36,p.8403-8407]

Literature

Title: Formation of tubules by p-tert-butylphenylamide derivatives of chenodeoxycholic and ursodeoxycholic acids in aqueous solution.

Journal: Steroids 20121001

Title: Supramolecular structures generated by a p-tert-butylphenylamide derivative of deoxycholic acid. From planar sheets to tubular structures through helical ribbons.

Journal: Langmuir : the ACS journal of surfaces and colloids 20100601

Title: Cytotoxicity and acid ceramidase inhibitory activity of 2-substituted aminoethanol amides.

Journal: Chemistry and physics of lipids 20081101

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