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Home Deuterated Building Blocks 6368-20-3
6368-20-3,MFCD26792600
Catalog No.:AA003OE1

6368-20-3 | Boc-D-Serine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$6.00   $4.00
- +
10g
98%
in stock  
$9.00   $7.00
- +
25g
98%
in stock  
$16.00   $11.00
- +
100g
98%
in stock  
$50.00   $35.00
- +
500g
98%(HPLC)
in stock  
$239.00   $167.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003OE1
Chemical Name:
Boc-D-Serine
CAS Number:
6368-20-3
Molecular Formula:
C8H15NO5
Molecular Weight:
205.2084
MDL Number:
MFCD26792600
SMILES:
OC[C@H](C(=O)O)NC(=O)OC(C)(C)C
Properties
Properties
 
BP:
385.1°C at 760 mmHg  
Form:
Solid  
MP:
91-95 °C(lit.)  
Refractive Index:
1.4540 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
220  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
5  
XLogP3:
-0.1  

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1994,vol.116,p.8402-8403

[2]JournaloftheAmericanChemicalSociety,2008,vol.130,p.2351-2364

[3]AdvancedSynthesisandCatalysis,2016,vol.358,p.34-40

[4]Patent:CN104030943,2016,B.Locationinpatent:Paragraph0095;0096

[5]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.1114-1120

[6]MedicinalChemistry,2014,vol.10,p.609-618

[7]ChineseChemicalLetters,2012,vol.23,p.661-664

[8]Patent:US2014/323738,2014,A1.Locationinpatent:Paragraph0042

[9]Patent:CN106957239,2017,A.Locationinpatent:Paragraph0036-0039

[10]Patent:US2003/166616,2003,A1

[11]Patent:EP1338592,2003,A1

[12]Patent:US2011/34731,2011,A1.Locationinpatent:Page/Pagecolumn7

[13]EuropeanJournalofMedicinalChemistry,2018,vol.143,p.1489-1509

[14]TetrahedronLetters,1989,vol.30,p.7021-7024

[15]TetrahedronLetters,1989,vol.30,p.3027-3028

[16]JournalofOrganicChemistry,1987,vol.52,p.2361-2364

[17]TetrahedronLetters,1993,vol.34,p.6705-6708

[18]Tetrahedron,1995,vol.51,p.8121-8134

[19]TetrahedronLetters,1995,vol.36,p.6235-6238

[20]Synthesis,1998,p.1707-1709

[21]Bioorganicandmedicinalchemistryletters,2003,vol.13,p.237-240

[22]OrganicLetters,2003,vol.5,p.4253-4256

[23]JournalofOrganicChemistry,2005,vol.70,p.2430-2438

[24]JournalofOrganicChemistry,2009,vol.74,p.4149-4157

[25]Patent:US2004/14816,2004,A1.Locationinpatent:Page/Pagecolumn11

[26]Tetrahedron,2010,vol.66,p.5384-5395

[27]NatureChemistry,2010,vol.2,p.280-285

[28]OrganicandBiomolecularChemistry,2011,vol.9,p.1356-1365

[29]Patent:WO2011/95995,2011,A1.Locationinpatent:Page/Pagecolumn10-11

[30]Patent:WO2011/99033,2011,A1.Locationinpatent:Page/Pagecolumn42

[31]Patent:WO2012/1710,2012,A1.Locationinpatent:Page/Pagecolumn10-12;18

[32]Patent:WO2012/46245,2012,A1.Locationinpatent:Page/Pagecolumn7

[33]ChemMedChem,2012,vol.7,p.1230-1236

[34]Patent:US2013/35508,2013,A1.Locationinpatent:Paragraph0031

[35]Patent:US2013/102811,2013,A1.Locationinpatent:Paragraph0041

[36]Patent:WO2014/155264,2014,A1.Locationinpatent:Page/Pagecolumn11-12

[37]ACSMedicinalChemistryLetters,2015,vol.6,p.537-542

[38]JournalofMedicinalChemistry,2015,vol.58,p.4204-4219

[39]Patent:WO2016/44770,2016,A1.Locationinpatent:Page/Pagecolumn732;733

[40]JournalofPeptideScience,2017,vol.23,p.202-214

[41]OrganicSyntheses,1992,vol.70,p.18-18

[42]Patent:WO2018/60781,2018,A1.Locationinpatent:Page/Pagecolumn16-17

[43]JournalofOrganicChemistry,2018,vol.83,p.7085-7101

[44]Patent:CN109180532,2019,A.Locationinpatent:Paragraph0016;0017

[1]Hashimoto,Makoto;Yoshida,Takuma;Tachrim,ZetryanaPuteri;Sakihama,Yasuko;Hashidoko,Yasuyuki;Hatanaka,Yasumaru;Kanaoka,Yuichi[Heterocycles,2017,vol.95,#1,p.462-473]

Literature
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