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Home Amines 7764-95-6
7764-95-6,MFCD26383924
Catalog No.:AA003ODH

7764-95-6 | (R)-2-((tert-Butoxycarbonyl)amino)propanoic acid hydrate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$8.00   $6.00
- +
10g
98%
in stock  
$11.00   $8.00
- +
50g
95%
in stock  
$18.00   $13.00
- +
500g
98%
in stock  
$153.00   $107.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003ODH
Chemical Name:
(R)-2-((tert-Butoxycarbonyl)amino)propanoic acid hydrate
CAS Number:
7764-95-6
Molecular Formula:
C8H15NO4
Molecular Weight:
189.2090
MDL Number:
MFCD26383924
SMILES:
C[C@H](C(=O)O)NC(=O)OC(C)(C)C
Properties
Properties
 
BP:
320.9 °C at 760 mmHg  
Form:
Solid  
MP:
81-84 °C  
Refractive Index:
26 ° (C=2, AcOH)  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
207  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
4  
XLogP3:
0.9  

Downstream Synthesis Route
338-69-2    24424-99-5   
Boc-(R)-Ala 

[1]CurrentPatentAssignee:HAISCOPHARMACEUTICALGROUPCO.,LTD.-EP3656782,2020,A1Locationinpatent:Paragraph0228

[2]CurrentPatentAssignee:NORTH&SOUTHBROTHERPHARMACYINVESTMENTCOMPANYLTD;SHENZHENDONGYANGGUANGINDUSTRIALDEVELOPMENTCOLTD-WO2019/144864,2019,A1Locationinpatent:Paragraph00227;00283

[3]CurrentPatentAssignee:NANCHANGUNIVERSITY-CN108148017,2018,ALocationinpatent:Paragraph0037;0038

[4]Schwyzer;Do;Eberle;Fauchere[HelveticaChimicaActa,1981,vol.64,#7,p.2078-2083]

[5]Gao,Min;He,Junhua;Xu,Weidong;Lai,Xiaoping;Liu,Fen;Tu,Guogang[Pharmazie,2018,vol.73,#3,p.123-127]

[6]Kokan,Zoran;Perić,Berislav;Vazdar,Mario;Marinić,Željko;Vikić-Topić,Dražen;Meštrović,Ernest;Kirin,SrećkoI.[ChemicalCommunications,2017,vol.53,#12,p.1945-1948]

[7]Wolf;Pfander[HelveticaChimicaActa,1986,vol.69,#6,p.1498-1504]

[8]Gao,Guangzheng;Sanda,Fumio;Masuda,Toshio[Macromolecules,2003,vol.36,#11,p.3938-3943]

[9]Mayer;Wimmer;Dillon-Carter;Partilla;Burchardt;Mihovilovic;Baumann;Sitte[BritishJournalofPharmacology,2016,p.2657-2668]

[10]CurrentPatentAssignee:SHENZHENDONGYANGGUANGINDUSTRIALDEVELOPMENTCOLTD-CN108341752,2018,ALocationinpatent:Paragraph0317;0319;0320;0321

[11]Lucet,Denis;LeGall,Thierry;Mioskowski,Charles;Ploux,Olivier;Marquet,Andree[TetrahedronAsymmetry,1996,vol.7,#4,p.985-988]

[12]Pastor,IsidroM.;Vaestilae,Patrik;Adolfsson,Hans[Chemistry-AEuropeanJournal,2003,vol.9,#17,p.4031-4045]

[13]Jakopin,Žiga;Roškar,Robert;Dolenc,MarijaSollner[TetrahedronLetters,2007,vol.48,#8,p.1465-1468]

[14]Locationinpatent:experimentalpartYan,Jincan;Wang,Lei[Synthesis,2008,#13,p.2065-2072]

[15]Locationinpatent:experimentalpartSchwarz,Stefan;Csuk,René[BioorganicandMedicinalChemistry,2010,vol.18,#21,p.7458-7474]

[16]CurrentPatentAssignee:AUTIFONYTHERAPEUTICSLIMITED-WO2011/69951,2011,A1Locationinpatent:Page/Pagecolumn50

[17]Csuk,Rene;Schwarz,Stefan;Siewert,Bianka;Kluge,Ralph;Stroehl,Dieter[ZeitschriftfurNaturforschung,B:ChemicalSciences,2012,vol.67,#7,p.731-746]

[18]CurrentPatentAssignee:Novartis(w/oSandoz);NOVARTISAG-WO2013/8162,2013,A1Locationinpatent:Page/Pagecolumn93

[19]CurrentPatentAssignee:ABBVIEINC-WO2016/44770,2016,A1Locationinpatent:Page/Pagecolumn698

[20]CurrentPatentAssignee:RUYUANYAOAUTONOMOUSCOUNTYDAZHONGDRUGTRADING-CN105503826,2016,ALocationinpatent:Paragraph0046;0047;0048

[21]Pidugu,VijayaRao;Yarla,NagendraSastry;Pedada,SrinivasaRao;Kalle,ArunasreeM.;Satya,A.Krishna[BioorganicandMedicinalChemistry,2016,vol.24,#21,p.5611-5617]

[22]CurrentPatentAssignee:YANG,XUECONG;ZHAO,LEI;LIU,JIANG;HUANG,XINQUAN-CN106543253,2017,ALocationinpatent:Paragraph0092-0095

[23]CurrentPatentAssignee:LANZHOUUNIVERSITY-CN108690005,2018,ALocationinpatent:Paragraph0026;0027

[24]deCastro,PedroP.;Siqueira,RaoniP.;Conforte,Luiza;Franco,ChrisH.J.;Bressan,GustavoC.;Amarante,GiovanniW.[JournaloftheBrazilianChemicalSociety,2020,vol.31,#1,p.193-200]

[1]Haviv;Fitzpatrick;Nichols;Swenson;Mort;Bush;Diaz;Nguyen;Holst;Cybulski;etal.[Journalofmedicinalchemistry,1993,vol.36,#7,p.928-933]

[1]CurrentPatentAssignee:ABBVIEINC-US2016/75692,2016,A1Locationinpatent:Paragraph0695

[2]CurrentPatentAssignee:MERCK&COINC-WO2009/58298,2009,A1Locationinpatent:Page/Pagecolumn145

[3]CurrentPatentAssignee:MERCK&COINC-WO2009/58299,2009,A1Locationinpatent:Page/Pagecolumn60-61

[4]CurrentPatentAssignee:MERCK&COINC-WO2010/111058,2010,A1Locationinpatent:Page/Pagecolumn64

[5]CurrentPatentAssignee:MERCK&COINC-WO2010/111059,2010,A1Locationinpatent:Page/Pagecolumn49

[6]CurrentPatentAssignee:MERCK&COINC-EP2411001,2018,B1Locationinpatent:Paragraph0118

[1]CurrentPatentAssignee:GOVERNMENTOFTHEUNITEDSTATES;UNIVERSITYOFMIAMI-US2014/179604,2014,A1Locationinpatent:Paragraph0192;0401-0405

13734-41-3    13139-16-7    13139-15-6    15761-38-3    7536-55-2   
Boc-(R)-Ala 
  13726-85-7    13734-34-4    15260-10-3    34306-42-8    13836-37-8    93288-03-0    23680-31-1    73821-95-1    47689-67-8    6404-28-0    144183-31-3   
N-tert-butoxycarbonyl-N'-(2-chlorobenzyloxycarbonyl)-L-ornithine 
 
Dat-D-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Orn-Val-Leu-Abu-Gln-Leu-Ser-Ala-Arg-Orn-Leu-Leu-Gln-Asp-Ile-Nle-Asp-Arg-Amc-NH2 

[1]CurrentPatentAssignee:UNIVERSITYOFMIAMI;GOVERNMENTOFTHEUNITEDSTATES-US2014/179604,2014,A1Locationinpatent:Paragraph0192;0270-0272

Literature

Title: Microspheres consisting of optically active helical substituted polyacetylenes: preparation via suspension polymerization and their chiral recognition/release properties.

Journal: Macromolecular rapid communications 20111215

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Tags:7764-95-6 Molecular Formula|7764-95-6 MDL|7764-95-6 SMILES|7764-95-6 (R)-2-((tert-Butoxycarbonyl)amino)propanoic acid hydrate