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14289-45-3,MFCD07698693
Catalog No.:AA01DVYQ

14289-45-3 | 2-(naphthalen-2-yl)-2-oxoacetic acid

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500mg
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$458.00   $320.00
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1g
97%
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$654.00   $458.00
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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:
AA01DVYQ
Chemical Name:
2-(naphthalen-2-yl)-2-oxoacetic acid
CAS Number:
14289-45-3
Molecular Formula:
C12H8O3
Molecular Weight:
200.1901
MDL Number:
MFCD07698693
SMILES:
OC(=O)C(=O)c1ccc2c(c1)cccc2
Properties
Computed Properties
 
Complexity:
272  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
3.2  

Downstream Synthesis Route

[1]Blicke;Feldkamp[JournaloftheAmericanChemicalSociety,1944,vol.66,p.1087,1090]

[2]Chiba,Shunsuke;Zhang,Line;Lee,Jian-Yuan[JournaloftheAmericanChemicalSociety,2010,vol.132,#21,p.7266-7267]

[3]Weng,Jian-Quan;Deng,Qiao-Man;Wu,Liang;Xu,Kai;Wu,Hao;Liu,Ren-Rong;Gao,Jian-Rong;Jia,Yi-Xia[OrganicLetters,2014,vol.16,#3,p.776-779]

[4]Shirai,Tomohiko;Ito,Hajime;Yamamoto,Yasunori[AngewandteChemie-InternationalEdition,2014,vol.53,#10,p.2658-2661][Angew.Chem.,2014,vol.126,#10,p.2696-2699,4]

[5]Enders,Dieter;Stöckel,BiancaA.;Rembiak,Andreas[ChemicalCommunications,2014,vol.50,#34,p.4489-4491]

[6]CurrentPatentAssignee:BIOMARINPHARMACEUTICALINC-WO2015/42397,2015,A1Locationinpatent:Paragraph000854

[7]Li,Bowen;Aliyu,MuinatA.;Gao,Zhenhua;Li,Tiejun;Dong,Wei;Li,Junchen;Shi,Enxue;Tang,Wenjun[OrganicLetters,2020,vol.22,#13,p.4974-4978]

[1]AdvancedSynthesisandCatalysis,2006,vol.348,p.2183-2190

14289-45-3   
potassiumphenyltrifluoborate 
  644-13-3 

[1]Li,Mingzong;Wang,Cong;Ge,Haibo[OrganicLetters,2011,vol.13,#8,p.2062-2064]

14289-45-3    4783-68-0   
naphthalen-2-yl(2-(pyridin-2-yloxy)phenyl)methanone 

[1]AdvancedSynthesisandCatalysis,2013,vol.355,p.1517-1522

[1]Chemistry-AEuropeanJournal,2014,vol.20,p.245-252

[2]JournalofOrganicChemistry,2019,vol.84,p.10962-10977

Literature

Title: alpha-Ketocarboxylic acid-based inhibitors of protein tyrosine phosphatases.

Journal: Bioorganic & medicinal chemistry letters 20010723

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