Home Amines 21911-84-2
21911-84-2,MFCD00089334
Catalog No.:AA00BD61

21911-84-2 | 3-Phenylamino-propionic acid methyl ester

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1g
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5g
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$170.00   $119.00
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10g
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$278.00   $195.00
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25g
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00BD61
Chemical Name:
3-Phenylamino-propionic acid methyl ester
CAS Number:
21911-84-2
Molecular Formula:
C10H13NO2
Molecular Weight:
179.2157
MDL Number:
MFCD00089334
SMILES:
COC(=O)CCNc1ccccc1
NSC Number:
144467
Properties
Computed Properties
 
Complexity:
153  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
5  
XLogP3:
2.3  

Upstream Synthesis Route

[1]TetrahedronLetters,2006,vol.47,#48,p.8583-8586

[2]OrganicLetters,2011,vol.13,#15,p.4008-4011

[1]SyntheticCommunications,2009,vol.39,#6,p.1109-1119

[2]RSCAdvances,2016,vol.6,#98,p.95951-95956

[3]MonatsheftefurChemie,2008,vol.139,#9,p.1041-1047

[4]InorganicChemistryCommunications,2015,vol.53,p.92-96

[5]Tetrahedron,2013,vol.69,#6,p.1712-1716

[6]Tetrahedron,2010,vol.66,#5,p.1091-1097

[7]CatalysisLetters,2018,vol.148,#9,p.2918-2928

[8]AsianJournalofChemistry,2011,vol.23,#9,p.3792-3794

[9]ComptesRendusChimie,2011,vol.14,#12,p.1059-1064

[10]MonatsheftefurChemie,2012,vol.143,#1,p.109-112

[11]TetrahedronLetters,2006,vol.47,#13,p.2125-2127

[12]JournaloftheChineseChemicalSociety,2010,vol.57,#6,p.1221-1226

[13]JournaloftheIranianChemicalSociety,2011,vol.8,#3,p.775-781

[14]IndianJournalofHeterocyclicChemistry,2010,vol.20,#2,p.169-170

[15]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2005,vol.44,#4,p.838-841

[16]TetrahedronLetters,2016,vol.57,#46,p.5026-5032

[17]RSCAdvances,2015,vol.5,#51,p.40950-40952

[18]TetrahedronLetters,2006,vol.47,#48,p.8583-8586

[19]Synthesis,2008,#24,p.3931-3936

[20]OrganicProcessResearchandDevelopment,2008,vol.12,#6,p.1078-1088

[21]SyntheticCommunications,2013,vol.43,#2,p.191-197,7

[22]OrganicProcessResearchandDevelopment,2008,vol.12,#1,p.41-57

[23]OrganicPreparationsandProceduresInternational,2013,vol.45,#1,p.28-43

[24]SyntheticCommunications,2010,vol.40,#19,p.2830-2836

[25]JournalofOrganicChemistry,2016,vol.81,#10,p.4048-4057

[26]OrganicLetters,2016,vol.18,#23,p.6140-6143

[27]JournalofOrganometallicChemistry,2003,vol.665,#1-2,p.250-257

[28]Tetrahedron,2010,vol.66,#29,p.5373-5377

[29]Synlett,1998,#9,p.975-976

[30]ChemicalCommunications,2010,vol.46,#43,p.8234-8236

[31]JournalofOrganicChemistry,2009,vol.74,#16,p.6260-6265

[32]Tetrahedron,2004,vol.60,#2,p.383-387

[33]Tetrahedron,2006,vol.62,#4,p.672-677

[34]Tetrahedron,2007,vol.63,#4,p.904-909

[35]Patent:US2008/9482,2008,A1,.Locationinpatent:Page/Pagecolumn121

[36]ResearchonChemicalIntermediates,2011,vol.37,#8,p.883-890

[37]JournaloftheAmericanChemicalSociety,1949,vol.71,p.2532,2537

[38]JournaloftheAmericanChemicalSociety,1949,vol.71,p.1901,1905

[39],1967,vol.3,p.520-526

[40]ZhurnalOrganicheskoiKhimii,1967,vol.3,p.542-550

[41]Synthesis,1981,#5,p.375-376

[42]EuropeanJournalofMedicinalChemistry,1993,vol.28,#11,p.837-852

[43]JournaloftheAmericanChemicalSociety,2006,vol.128,#5,p.1446-1447

[44]Tetrahedron,2007,vol.63,#29,p.6764-6773

[45]TetrahedronLetters,2007,vol.48,#49,p.8735-8738

[46]OrganicandBiomolecularChemistry,2009,vol.7,#11,p.2452-2457

[47]Synlett,2010,#3,p.379-382

[48]TetrahedronLetters,2010,vol.51,#33,p.4455-4458

[49]ComptesRendusChimie,2011,vol.14,#11,p.973-977

[50]ACSCatalysis,2013,vol.3,#12,p.2891-2904

[51]Organometallics,2013,vol.32,#23,p.6986-6995

[52]ProcessBiochemistry,2016,vol.51,#10,p.1420-1433

[1]Tetrahedron,2011,vol.67,#1,p.167-172

[1]Tetrahedron,2014,vol.70,#14,p.2449-2454

[2]JournalofOrganicChemistry,2009,vol.74,#16,p.6260-6265

[1]OrganicandBiomolecularChemistry,2015,vol.13,#16,p.4637-4641

Downstream Synthesis Route

[1]Patent:US2470094,1945,

[1]JournaloftheAmericanChemicalSociety,1959,vol.81,p.5957,5959

[1]Arzneimittel-Forschung/DrugResearch,1973,vol.23,p.290-295

[1]Arzneimittel-Forschung/DrugResearch,1973,vol.23,p.290-295

[1]Arzneimittel-Forschung/DrugResearch,1973,vol.23,p.290-295

Literature
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SDS
Tags:21911-84-2 Molecular Formula|21911-84-2 MDL|21911-84-2 SMILES|21911-84-2 3-Phenylamino-propionic acid methyl ester