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Home Other Building Blocks 1115-59-9
1115-59-9,MFCD00063662
Catalog No.:AA003506

1115-59-9 | L-Alanine ethyl ester HCl

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$19.00   $14.00
- +
25g
98%
in stock  
$25.00   $18.00
- +
100g
98%
in stock  
$74.00   $52.00
- +
500g
98%
in stock  
$150.00   $105.00
- +
  • 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:
AA003506
Chemical Name:
L-Alanine ethyl ester HCl
CAS Number:
1115-59-9
Molecular Formula:
C5H12ClNO2
Molecular Weight:
153.6073
MDL Number:
MFCD00063662
SMILES:
CCOC(=O)[C@@H](N)C.Cl
Properties
Properties
 
Form:
Solid  
MP:
62 °C  
Solubility:
100g/l  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
82.5  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
3  

Upstream Synthesis Route

[1]Patent:US5162307,1992,A,

[1]ChemicalCommunications,2011,vol.47,#26,p.7347-7349

[2]DaltonTransactions,2015,vol.44,#3,p.1170-1177

[3]Tetrahedron,1999,vol.55,#11,p.3337-3354

[4]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2006,vol.45,#8,p.1942-1944

[5]JournaloftheChemicalSociety,PerkinTransactions2:PhysicalOrganicChemistry(1972-1999),1994,#7,p.1455-1462

[6]ACSMedicinalChemistryLetters,2016,vol.7,#12,p.1197-1201

[7]EuropeanJournalofInorganicChemistry,2003,#11,p.2113-2122

[8]JournaloftheChemicalSociety,FaradayTransactions1:PhysicalChemistryinCondensedPhases,1980,vol.76,p.915-922

[9]JournaloftheIndianChemicalSociety,2001,vol.78,#3,p.137-141

[10]EuropeanJournalofMedicinalChemistry,2011,vol.46,#1,p.11-20

[11]Tetrahedron,2008,vol.64,#7,p.1301-1308

[12]ChemistryofNaturalCompounds,1994,vol.30,#2,p.238-244

[13]KhimiyaPrirodnykhSoedinenii,1994,#2,p.261-268

[14]Tetrahedron,1990,vol.46,#15,p.5325-5332

[15]JournalofOrganometallicChemistry,1981,vol.221,#2,p.203-222

[16]HelveticaChimicaActa,1995,vol.78,p.109-121

[17]Tetrahedron,2007,vol.63,#14,p.3031-3041

[18]AdvancedSynthesisandCatalysis,2012,vol.354,#2-3,p.295-300

[19]GreenChemistry,2012,vol.14,#5,p.1350-1356

[20]ChemistryofNaturalCompounds,2012,vol.48,#2,p.194-197

[21]Tetrahedron,2012,vol.68,#49,p.10218-10229,12

[22]Tetrahedron,2012,vol.68,#49,p.10218-10229

[23]Nucleosides,NucleotidesandNucleicAcids,2013,vol.32,#4,p.161-173

[24]Patent:US2016/264611,2016,A1,.Locationinpatent:Paragraph0222;0223;0224

[25]InternationalJournalofPharmaceutics,2018,vol.546,#1-2,p.31-38

[1]Patent:US5801249,1998,A,

[1]EuropeanJournalofMedicinalChemistry,2009,vol.44,#9,p.3765-3770

[1]TetrahedronAsymmetry,1999,vol.10,#3,p.411-427

Downstream Synthesis Route

[1]CanadianJournalofChemistry,1976,vol.54,p.733-737

1115-59-9   
phenylmagnesiumbromide 
  78603-91-5 

[1]JournaloftheChemicalSociety.PerkintransactionsII,1994,p.1455-1462

[2]CollectionofCzechoslovakChemicalCommunications,1968,vol.33,p.1911-1916

52449-98-6    1115-59-9   
(S)-2-((S)-Tetrahydro-furan-2-carbonyl)-amino-propionicacidethylester 
 
(S)-2-((R)-Tetrahydro-furan-2-carbonyl)-amino-propionicacidethylester 

[1]AngewandteChemie,1993,vol.105,p.785-786

[1]TetrahedronLetters,2017,vol.58,p.860-863

[2]Tetrahedron,1983,vol.39,p.3419

[1]ChemicalCommunications,2011,vol.47,p.7347-7349

[2]DaltonTransactions,2015,vol.44,p.1170-1177

[3]EuropeanJournalofMedicinalChemistry,2020,vol.190

[4]Tetrahedron,1999,vol.55,p.3337-3354

[5]ChemicalCommunications,2020,vol.56,p.3373-3376

[6]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2006,vol.45,p.1942-1944

[7]JournaloftheChemicalSociety.PerkintransactionsII,1994,p.1455-1462

[8]ACSMedicinalChemistryLetters,2016,vol.7,p.1197-1201

[9]EuropeanJournalofInorganicChemistry,2003,p.2113-2122

[10]JournaloftheChemicalSociety,FaradayTransactions1:PhysicalChemistryinCondensedPhases,1980,vol.76,p.915-922

[11]JournaloftheIndianChemicalSociety,2001,vol.78,p.137-141

[12]EuropeanJournalofMedicinalChemistry,2011,vol.46,p.11-20

[13]Tetrahedron,2008,vol.64,p.1301-1308

[14]ChemistryofNaturalCompounds,1994,vol.30,p.238-244    KhimiyaPrirodnykhSoedinenii,1994,p.261-268

[15]Tetrahedron,1990,vol.46,p.5325-5332

[16]JournalofOrganometallicChemistry,1981,vol.221,p.203-222

[17]HelveticaChimicaActa,1995,vol.78,p.109-121

[18]Tetrahedron,2007,vol.63,p.3031-3041

[19]AdvancedSynthesisandCatalysis,2012,vol.354,p.295-300

[20]GreenChemistry,2012,vol.14,p.1350-1356

[21]ChemistryofNaturalCompounds,2012,vol.48,p.194-197

[22]Tetrahedron,2012,vol.68,p.10218-10229,12

[23]Nucleosides,nucleotidesandnucleicacids,2013,vol.32,p.161-173

[24]Patent:US2016/264611,2016,A1.Locationinpatent:Paragraph0222;0223;0224

[25]InternationalJournalofPharmaceutics,2018,vol.546,p.31-38

[26]RSCAdvances,2019,vol.9,p.26302-26314

[27]BioorganicChemistry,2020,vol.99

Literature
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SDS
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