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109183-71-3,MFCD02684452
Catalog No.:AA0034H9

109183-71-3 | Boc-L-cyclohexylglycine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$7.00   $5.00
- +
5g
97%
in stock  
$9.00   $7.00
- +
10g
97%
in stock  
$13.00   $9.00
- +
25g
97%
in stock  
$21.00   $15.00
- +
100g
97%
in stock  
$66.00   $47.00
- +
500g
97%
in stock  
$328.00   $230.00
- +
  • 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:
AA0034H9
Chemical Name:
Boc-L-cyclohexylglycine
CAS Number:
109183-71-3
Molecular Formula:
C13H23NO4
Molecular Weight:
257.3260
MDL Number:
MFCD02684452
SMILES:
O=C(OC(C)(C)C)N[C@@H](C1CCCCC1)C(=O)O
Properties
Properties
 
BP:
407.9°C at 760 mmHg  
Form:
Solid  
MP:
83°C(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
303  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
5  
XLogP3:
2.9  

Upstream Synthesis Route

[1]Bioorganicandmedicinalchemistryletters,2004,vol.14,#1,p.275-278

[2]BioorganicandMedicinalChemistryLetters,2009,vol.19,#4,p.1105-1109

[3]Patent:US6353006,2002,B1,.Locationinpatent:Pagecolumn111

[1]JournalofMedicinalChemistry,2017,vol.60,#13,p.5816-5825

[2]JournalofMedicinalChemistry,1993,vol.36,#1,p.166-172

[3]Patent:WO2004/22534,2004,A1,.Locationinpatent:Page54

[4]Bioorganicandmedicinalchemistryletters,2004,vol.14,#1,p.275-278

[5]BioorganicandMedicinalChemistryLetters,2011,vol.21,#6,p.1832-1837

[6]BioorganicandMedicinalChemistryLetters,2013,vol.23,#23,p.6325-6330

[7]JournalofOrganicChemistry,2015,vol.80,#15,p.7770-7778

[1]Patent:US5338726,1994,A,

[1]ChemicalandPharmaceuticalBulletin,1981,vol.29,#6,p.1644-1654

[2]JournalofMedicinalChemistry,1971,vol.14,p.899-903

[1]Patent:WO2011/144585,2011,A1,.Locationinpatent:Page/Pagecolumn136-137

Downstream Synthesis Route

[1]ChemicalandPharmaceuticalBulletin,1981,vol.29,p.1644-1654

[2]JournalofMedicinalChemistry,1971,vol.14,p.899-903

[1]JournalofMedicinalChemistry,2017,vol.60,p.5816-5825

[2]Patent:WO2018/226837,2018,A1.Locationinpatent:Paragraph00148

[3]JournalofMedicinalChemistry,1993,vol.36,p.166-172

[4]Patent:WO2004/22534,2004,A1.Locationinpatent:Page54

[5]Bioorganicandmedicinalchemistryletters,2004,vol.14,p.275-278

[6]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.1832-1837

[7]BioorganicandMedicinalChemistryLetters,2013,vol.23,p.6325-6330

[8]JournalofOrganicChemistry,2015,vol.80,p.7770-7778

[1]TetrahedronLetters,1994,vol.35,p.237-240

13734-41-3    72784-43-1    108-24-7    109183-71-3    652160-92-4   
1-(2S,4R)-1-(S)-2-((S)-2-Acetylamino-2-cyclohexyl-acetylamino)-3-methyl-butyryl-4-(2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carbonyl-amino}-cyclopropanecarboxylicacid 

[1]JournalofMedicinalChemistry,2004,vol.47,p.123-132

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.5007-5011

Literature
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SDS
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