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Home Other Building Blocks 21887-64-9
21887-64-9,MFCD00076970
Catalog No.:AA007OWH

21887-64-9 | Boc-Orn-OH

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$6.00   $4.00
- +
5g
97%
in stock  
$19.00   $14.00
- +
10g
97%
in stock  
$37.00   $26.00
- +
25g
97%
in stock  
$51.00   $36.00
- +
100g
97%
in stock  
$200.00   $140.00
- +
  • 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:
AA007OWH
Chemical Name:
Boc-Orn-OH
CAS Number:
21887-64-9
Molecular Formula:
C10H20N2O4
Molecular Weight:
232.2768
MDL Number:
MFCD00076970
SMILES:
NCCC[C@@H](C(=O)O)NC(=O)OC(C)(C)C
Properties
Computed Properties
 
Complexity:
248  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
7  
XLogP3:
-1.9  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,1996,vol.39,#23,p.4531-4536

[2]OrganicProcessResearchandDevelopment,2007,vol.11,#3,p.406-413

[3]OrganicandBiomolecularChemistry,2006,vol.4,#20,p.3769-3777

[4]BioorganicandMedicinalChemistry,2006,vol.14,#9,p.3185-3198

[5]JournalofOrganicChemistry,2011,vol.76,#5,p.1228-1238

[6]JournalfuerPraktischeChemie(Leipzig),1969,vol.311,p.3-8

[7]BioorganicandMedicinalChemistryLetters,2000,vol.10,#10,p.1077-1080

[8]JournaloftheAmericanChemicalSociety,2004,vol.126,#34,p.10598-10602

[9]Organicletters,2001,vol.3,#21,p.3229-3232

[10]EuropeanJournalofOrganicChemistry,2008,#31,p.5308-5314

[11]Patent:WO2011/143497,2011,A1,.Locationinpatent:Page/Pagecolumn48

[12]OrganicandBiomolecularChemistry,2015,vol.13,#15,p.4570-4580

[13]Synthesis(Germany),2017,vol.49,#8,p.1857-1866

[1]Patent:US6262047,2001,B1,

[1]JournaloftheAmericanChemicalSociety,2018,vol.140,#23,p.7116-7126

[1]Patent:WO2008/14811,2008,A1,.Locationinpatent:Page/Pagecolumn14-15

[1]AminoAcids,2010,vol.38,#4,p.1155-1164

Downstream Synthesis Route

[1]Semple;Rowley;Brunck;Ha-Uong;Minami;Owens;Tamura;Goldman;Siev;Ardecky;Carpenter;Ge;Richard;Nolan;Hakanson;Tulinsky;Nutt;Ripka[JournalofMedicinalChemistry,1996,vol.39,#23,p.4531-4536]

[2]Galaffu,Nicola;Man,SiudPui;Wilkes,RobinD.;Wilson,JohnR.H.[OrganicProcessResearchandDevelopment,2007,vol.11,#3,p.406-413]

[3]Jones,MatthewA.;Hislop,AndrewD.;Snaith,JohnS.[OrganicandBiomolecularChemistry,2006,vol.4,#20,p.3769-3777]

[4]Litzinger,ElizabethA.;Martasek,Pavel;Roman,LindaJ.;Silverman,RichardB.[BioorganicandMedicinalChemistry,2006,vol.14,#9,p.3185-3198]

[5]Jacobsen,yvind;Maekawa,Hiroaki;Ge,Nien-Hui;Goerbitz,CarlHenrik;Rongved,Pal;Ottersen,OlePetter;Amiry-Moghaddam,Mahmood;Klaveness,Jo[JournalofOrganicChemistry,2011,vol.76,#5,p.1228-1238]

[6]Arold,H.;Haller,K.[JournalfurpraktischeChemie(Leipzig1954),1969,vol.311,p.3-8]

[7]Maurer,TristanS.;Pan,Jianping;Booth,BrianP.;Kalman,ThomasI.;Fung,Ho-Leung[BioorganicandMedicinalChemistryLetters,2000,vol.10,#10,p.1077-1080]

[8]Link,A.James;Vink,MandyK.S.;Tirrell,DavidA.[JournaloftheAmericanChemicalSociety,2004,vol.126,#34,p.10598-10602]

[9]Wender;Jessop;Pattabiraman;Pelkey;VanDeusen[Organicletters,2001,vol.3,#21,p.3229-3232]

[10]Locationinpatent:experimentalpartIsaad,AlexandraLeChevalier;Barbetti,Francesca;Rovero,Paolo;D'Ursi,AnnaMaria;Chelli,Mario;Chorev,Michael;Papini,AnnaMaria[EuropeanJournalofOrganicChemistry,2008,#31,p.5308-5314]

[11]CurrentPatentAssignee:Novartis(w/oSandoz);NOVARTISAG-WO2011/143497,2011,A1Locationinpatent:Page/Pagecolumn48

[12]Isidro-Llobet,Albert;HadjeGeorgiou,Kathy;Galloway,WarrenR.J.D.;Giacomini,Elisa;Hansen,MetteR.;Méndez-Abt,Gabriela;Tan,YawSing;Carro,Laura;Sore,HannahF.;Spring,DavidR.[OrganicandBiomolecularChemistry,2015,vol.13,#15,p.4570-4580]

[13]Cramer,Jonathan;Klebe,Gerhard[Synthesis,2017,vol.49,#8,p.1857-1866]

[14]CurrentPatentAssignee:DESIGNTHERAPEUTICS-WO2021/158707,2021,A1Locationinpatent:Paragraph00844;001290;001291;001292

[1]JournalofMedicinalChemistry,1996,vol.39,p.4531-4536

[2]Patent:WO2016/118877,2016,A1.Locationinpatent:Paragraph00208

2106-49-2    21887-64-9   
(S)-2-tert-Butoxycarbonylamino-5-(2-chloro-6-nitro-phenylamino)-pentanoicacid 

[1]JournalofMedicinalChemistry,1998,vol.41,p.2636-2642

10576-12-2    21887-64-9   
Nα-Boc-Nω-hydroxy-N5-(1-iminoethyl)-L-ornithine 

[1]JournaloftheAmericanChemicalSociety,1999,vol.121,p.903-916

15761-39-4    127095-92-5    21887-64-9   
2-(acetyl-<i>tert</i>-butoxycarbonyl-amino)-3-phenyl-propionicacid 
 
Boc-L-Trp,Boc-D-Arg(Tos)-PAMresin 
 
Ac-Phe-Orn-Pro-D-Cha-Trp-D-Arg 

[1]JournalofMedicinalChemistry,1999,vol.42,p.1965-1974

Literature
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SDS
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