Home Amines 18144-43-9
18144-43-9,MFCD00017108
Catalog No.:AA0022TJ

18144-43-9 | Isopropyl 4-aminobenzoate

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1g
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$29.00   $20.00
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5g
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25g
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$51.00   $36.00
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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:
AA0022TJ
Chemical Name:
Isopropyl 4-aminobenzoate
CAS Number:
18144-43-9
Molecular Formula:
C10H13NO2
Molecular Weight:
179.2157
MDL Number:
MFCD00017108
SMILES:
CC(OC(=O)c1ccc(cc1)N)C
Properties
Properties
 
BP:
226.9°C at 760 mmHg  
Form:
Solid  
MP:
83 - 85℃  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
172  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2.5  

Downstream Synthesis Route

[1]Morogina;Nasibulin;Klyuev[PetroleumChemistry,1998,vol.38,#4,p.251-255]

[2]Adamsetal.[JournaloftheAmericanChemicalSociety,1926,vol.48,p.1768]

[3]Adamsetal.[JournaloftheAmericanChemicalSociety,1926,vol.48,p.1768]Brill[JournaloftheAmericanChemicalSociety,1921,vol.43,p.1323]

[4]Matsunaga;Miyajima[MolecularCrystalsandLiquidCrystals(1969-1991),1984,vol.104,#3-4,p.353-359]

[5]Voronin;Nasibulin;Klyuev[RussianJournalofOrganicChemistry,1997,vol.33,#11,p.1613-1615]

[6]Morogina;Nasibulin;Klyuev[PetroleumChemistry,1998,vol.38,#4,p.251-255]

[7]Kaur,Gurmeet;Narayanan,VenL.;Risbood,PrabhakarA.;Hollingshead,MelindaG.;Stinson,ShermanF.;Varma,RaviK.;Sausville,EdwardA.[BioorganicandMedicinalChemistry,2005,vol.13,#5,p.1749-1761]

[8]CurrentPatentAssignee:Bayer-FR2264804,1975,B1[Chem.Abstr.,1976,vol.84,#58989][Chem.Abstr.,1976,vol.84,#58989]

[9]CurrentPatentAssignee:Bayer&Co.-DE211801,1800,C[Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.9,p.972][Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.9,p.972]

[10]CurrentPatentAssignee:Bayer&Co.-DE211801,1800,C[Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.9,p.972][Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.9,p.972]

[1]Budeanuetal.[1955,vol.1,p.345,349][Chem.Abstr.,1957,p.10751]

[1]CurrentPatentAssignee:PFIZERINC-WO2010/116270,2010,A1Locationinpatent:Page/Pagecolumn28-29

[2]Kazemi,Foad;Kiasat,AliReza;Mombaini,Began[Phosphorus,SulfurandSiliconandtheRelatedElements,2004,vol.179,#6,p.1187-1191]

[3]CurrentPatentAssignee:Bayer&Co.-DE211801,1800,C[Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.9,p.972][Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.9,p.972]

[1]CurrentPatentAssignee:Bayer-FR2264804,1975,B1[Chem.Abstr.,1976,vol.84,#58989][Chem.Abstr.,1976,vol.84,#58989]

[1]Roclofsen,D.P.etal.[RecueildesTravauxChimiquesdesPays-Bas,1970,vol.89,p.193-210]

[2]Mai,VanHung;Nikonov,GeorgiiI.[Organometallics,2016,vol.35,#7,p.943-949]

Literature

Title: Butamben derivatives enhance BMP-2-stimulated commitment of C2C12 cells into osteoblasts with induction of voltage-gated potassium channel expression.

Journal: Bioorganic & medicinal chemistry letters 20111215

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

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