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Home Other Building Blocks 39994-75-7
39994-75-7,MFCD00037677
Catalog No.:AA0037FP

39994-75-7 | L-Threonine methyl ester, HCl

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$11.00   $8.00
- +
5g
97%
in stock  
$18.00   $13.00
- +
10g
97%
in stock  
$23.00   $16.00
- +
25g
97%
in stock  
$55.00   $39.00
- +
100g
98%
in stock  
$188.00   $132.00
- +
500g
98%
in stock  
$693.00   $485.00
- +
  • 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:
AA0037FP
Chemical Name:
L-Threonine methyl ester, HCl
CAS Number:
39994-75-7
Molecular Formula:
C5H12ClNO3
Molecular Weight:
169.6067
MDL Number:
MFCD00037677
SMILES:
COC(=O)[C@H]([C@H](O)C)N.Cl
Properties
Properties
 
Form:
Solid  
MP:
64 °C  
Stability:
Moisture Sensitive & Hygroscopic  
Storage:
Room Temperature;Light sensitive;Inert atmosphere;  

Computed Properties
 
Complexity:
104  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
2  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
3  

Upstream Synthesis Route

[1]ChemicalandPharmaceuticalBulletin,1985,vol.33,#4,p.1342-1350

[1]Patent:CN106631900,2017,A,.Locationinpatent:Paragraph0015

[2]JournaloftheChemicalSociety-PerkinTransactions1,1999,#24,p.3697-3703

[3]JustusLiebigsAnnalenderChemie,1962,vol.656,p.190-204

[4]JournalofOrganicChemistry,1985,vol.50,#23,p.4515-4523

[5]Patent:WO2010/17060,2010,A1,.Locationinpatent:Page/Pagecolumn44-45

[1]JournalofMedicinalChemistry,1995,vol.38,#15,p.2851-2859

[2]Synthesis,1999,#10,p.1739-1746

[3]SyntheticCommunications,2000,vol.30,#20,p.3685-3691

[4]BioorganicChemistry,2008,vol.36,#1,p.4-15

[5]Synlett,2009,#8,p.1227-1232

[6]BulletindesSocietesChimiquesBelges,1989,vol.98,#3,p.191-202

[7]TetrahedronAsymmetry,1996,vol.7,#1,p.293-299

[8]Polymer,2010,vol.51,#12,p.2479-2485

[9]JournalofOrganicChemistry,2002,vol.67,#5,p.1536-1547

[10]BioorganicandMedicinalChemistry,2007,vol.15,#14,p.4775-4799

[11]BioorganicandMedicinalChemistry,2007,vol.15,#18,p.6273-6290

[12]BioorganicandMedicinalChemistry,2008,vol.16,#4,p.1764-1774

[13]MedicinalChemistryResearch,2018,vol.27,#1,p.285-307

[14]OrganicandBiomolecularChemistry,2006,vol.4,#15,p.2888-2897

[15]Tetrahedron,2014,vol.70,#34,p.5082-5092

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

[17]JournalofOrganicChemistry,2003,vol.68,#26,p.9899-9906

[18]JournaloftheAmericanChemicalSociety,1992,vol.114,#26,p.10249-10258

[19]SyntheticCommunications,2010,vol.40,#8,p.1161-1179

[20]JournalofOrganicChemistry,1982,vol.47,#20,p.3850-3854

[21]JournalofOrganicChemistry,1985,vol.50,#23,p.4515-4523

[22]AngewandteChemie,1994,vol.106,#6,p.693-695

[23]TetrahedronLetters,1995,vol.36,#4,p.497-500

[24]Tetrahedron,1997,vol.53,#18,p.6473-6484

[25]JournalofOrganicChemistry,1997,vol.62,#21,p.7364-7375

[26]Tetrahedron,1999,vol.55,#42,p.12301-12308

[27]Patent:US2005/182262,2005,A1,.Locationinpatent:Page/Pagecolumn2

[28]Chemistry-AnAsianJournal,2009,vol.4,#2,p.328-335

[29]BioorganicandMedicinalChemistry,2010,vol.18,#6,p.2135-2140

[30]AsianJournalofChemistry,2012,vol.24,#3,p.1227-1236

[31]JournalofMedicinalChemistry,2012,vol.55,#22,p.9946-9957

[32]JournalofNaturalProducts,2013,vol.76,#7,p.1388-1391

[33]JournalofOrganicChemistry,2016,vol.81,#1,p.215-228

[34]Patent:CN106631900,2017,A,.Locationinpatent:Paragraph0015

[35]Patent:CN106674254,2017,A,.Locationinpatent:Paragraph0163-0167

[36]JournaloftheAmericanChemicalSociety,2017,vol.139,#38,p.13420-13428

[1]JournalofOrganicChemistry,1992,vol.57,#16,p.4331-4333

[2]JournaloftheAmericanChemicalSociety,1994,vol.116,#13,p.5607-5618

[1]BioorganicandMedicinalChemistryLetters,2013,vol.23,#8,p.2362-2367

Downstream Synthesis Route

[1]JournalofOrganicChemistry,2002,vol.67,p.1536-1547

[2]HelveticaChimicaActa,1957,vol.40,p.1531,1544

[3]JournalofOrganicChemistry,1997,vol.62,p.7364-7375

[4]JournalofOrganicChemistry,2003,vol.68,p.10046-10057

[5]JournaloftheAmericanChemicalSociety,2007,vol.129,p.6017-6021

[6]BioorganicandMedicinalChemistry,2011,vol.19,p.852-860

[7]JournalofNaturalProducts,2013,vol.76,p.1388-1391

[8]JournalofOrganicChemistry,2019,vol.84,p.10257-10279

[9]Tetrahedron,2019,vol.75

[1]HelveticaChimicaActa,1957,vol.40,p.1531,1544

[1]Patent:CN106631900,2017,A.Locationinpatent:Paragraph0015

[2]JournaloftheChemicalSociety.PerkintransactionsI,1999,p.3697-3703

[3]JustusLiebigsAnnalenderChemie,1962,vol.656,p.190-204

[4]JournalofOrganicChemistry,1985,vol.50,p.4515-4523

[5]Patent:WO2010/17060,2010,A1.Locationinpatent:Page/Pagecolumn44-45

[1]LiebigsAnnalenderChemie,1990,p.569-579

39994-75-7   
methyl4-phenylbutanimidatehydrochloride 
 
(4S,5R)-2-(3-phenylpropyl)-4-carbomethoxy-5-methyl-2-oxazoline 

[1]Tetrahedron,1994,vol.50,p.5083-5090

Literature

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology 20090101

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SDS
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