52558-24-4,MFCD17215355
Catalog No.:AA00DKE7

52558-24-4 | N-tert-Butyloxycarbonyl-(S)-isoserine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
98%
in stock  
$12.00   $8.00
- +
250mg
98%
in stock  
$22.00   $16.00
- +
1g
98%
in stock  
$66.00   $46.00
- +
5g
95%
in stock  
$170.00   $119.00
- +
10g
95%
in stock  
$329.00 $230.00
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00DKE7
Chemical Name:
N-tert-Butyloxycarbonyl-(S)-isoserine
CAS Number:
52558-24-4
Molecular Formula:
C8H15NO5
Molecular Weight:
205.2084
MDL Number:
MFCD17215355
SMILES:
O[C@H](C(=O)O)CNC(=O)OC(C)(C)C
Properties
Computed Properties
 
Complexity:
220  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.1  

Synonyms
 
  
Upstream Synthesis Route

[1]JournalofEnzymeInhibitionandMedicinalChemistry,2012,vol.27,#2,p.302-310

[2]JournalofOrganicChemistry,2018,vol.83,#9,p.4973-4980

[3]Patent:CN108341752,2018,A,.Locationinpatent:Paragraph0507;0508;0509;0510

[4]Patent:WO2010/132757,2010,A2,.Locationinpatent:Page/Pagecolumn98-99

[5]Patent:WO2011/44503,2011,A1,.Locationinpatent:Page/Pagecolumn67

[6]Patent:WO2011/44538,2011,A1,.Locationinpatent:Page/Pagecolumn94

[7]Patent:WO2009/67692,2009,A1,.Locationinpatent:Page/Pagecolumn60-61

[8]Patent:WO2010/42851,2010,A1,.Locationinpatent:Page/Pagecolumn55-56

[9]Patent:WO2010/132777,2010,A2,.Locationinpatent:Page/Pagecolumn63-64

[10]Patent:WO2013/169704,2013,A2,.Locationinpatent:Paragraph0261

[11]Chemicalandpharmaceuticalbulletin,2002,vol.50,#2,p.239-252

[12]Patent:WO2011/44498,2011,A1,.Locationinpatent:Page/Pagecolumn69-70

[13]JournalofEnzymeInhibitionandMedicinalChemistry,2013,vol.28,#4,p.717-726

[1]Patent:WO2010/42850,2010,A1,.Locationinpatent:Page/Pagecolumn55-56

[1]Synlett,2002,#12,p.2101-2103

[1]Synlett,2002,#12,p.2101-2103

Downstream Synthesis Route

[1]Synlett,2002,p.2101-2103

52558-24-4   
((R)-2-Mercapto-2-{(S)-1-(S)-2-(4-methoxy-phenyl)-1-methylcarbamoyl-ethylcarbamoyl-3-methyl-butylcarbamoyl}-ethyl)-carbamicacidtert-butylester 

[1]Chemicalandpharmaceuticalbulletin,2002,vol.50,p.239-252

[1]Chemicalandpharmaceuticalbulletin,2002,vol.50,p.239-252

52558-24-4   
Methanesulfonicacid(S)-2-tert-butoxycarbonylamino-1-{(S)-1-(S)-2-(4-methoxy-phenyl)-1-methylcarbamoyl-ethylcarbamoyl-3-methyl-butylcarbamoyl}-ethylester 

[1]Chemicalandpharmaceuticalbulletin,2002,vol.50,p.239-252

21715-90-2    52558-24-4   
C17H22N2O7 

[1]Patent:WO2009/67692,2009,A1.Locationinpatent:Page/Pagecolumn61-62

[2]Patent:WO2009/67692,2009,A1.Locationinpatent:Page/Pagecolumn71

Literature
Quotation Request
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Additional Info:
SDS
Tags:52558-24-4 Molecular Formula|52558-24-4 MDL|52558-24-4 SMILES|52558-24-4 N-tert-Butyloxycarbonyl-(S)-isoserine
Catalog No.: AA00DKE7
52558-24-4,MFCD17215355
52558-24-4 | N-tert-Butyloxycarbonyl-(S)-isoserine
Pack Size: 100mg
Purity: 98%
in stock
$12.00 $8.00
Pack Size: 250mg
Purity: 98%
in stock
$22.00 $16.00
Pack Size: 1g
Purity: 98%
in stock
$66.00 $46.00
Pack Size: 5g
Purity: 95%
in stock
$170.00 $119.00
Pack Size: 10g
Purity: 95%
in stock
$329.00 $230.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00DKE7
Chemical Name: N-tert-Butyloxycarbonyl-(S)-isoserine
CAS Number: 52558-24-4
Molecular Formula: C8H15NO5
Molecular Weight: 205.2084
MDL Number: MFCD17215355
SMILES: O[C@H](C(=O)O)CNC(=O)OC(C)(C)C
Properties
Complexity: 220  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.1  
35:   
Upstream Synthesis Route
565-71-9    24424-99-5    52558-24-4 

[1]JournalofEnzymeInhibitionandMedicinalChemistry,2012,vol.27,#2,p.302-310

[2]JournalofOrganicChemistry,2018,vol.83,#9,p.4973-4980

[3]Patent:CN108341752,2018,A,.Locationinpatent:Paragraph0507;0508;0509;0510

[4]Patent:WO2010/132757,2010,A2,.Locationinpatent:Page/Pagecolumn98-99

[5]Patent:WO2011/44503,2011,A1,.Locationinpatent:Page/Pagecolumn67

[6]Patent:WO2011/44538,2011,A1,.Locationinpatent:Page/Pagecolumn94

[7]Patent:WO2009/67692,2009,A1,.Locationinpatent:Page/Pagecolumn60-61

[8]Patent:WO2010/42851,2010,A1,.Locationinpatent:Page/Pagecolumn55-56

[9]Patent:WO2010/132777,2010,A2,.Locationinpatent:Page/Pagecolumn63-64

[10]Patent:WO2013/169704,2013,A2,.Locationinpatent:Paragraph0261

[11]Chemicalandpharmaceuticalbulletin,2002,vol.50,#2,p.239-252

[12]Patent:WO2011/44498,2011,A1,.Locationinpatent:Page/Pagecolumn69-70

[13]JournalofEnzymeInhibitionandMedicinalChemistry,2013,vol.28,#4,p.717-726

565-71-9    24424-99-5    56-40-6    52558-24-4 

[1]Patent:WO2010/42850,2010,A1,.Locationinpatent:Page/Pagecolumn55-56

169688-48-6    52558-24-4 

[1]Synlett,2002,#12,p.2101-2103

24424-99-5    52558-24-4 

[1]Synlett,2002,#12,p.2101-2103

Downstream Synthesis Route
24424-99-5    52558-24-4 

[1]Synlett,2002,p.2101-2103

52558-24-4   
((R)-2-Mercapto-2-{(S)-1-(S)-2-(4-methoxy-phenyl)-1-methylcarbamoyl-ethylcarbamoyl-3-methyl-butylcarbamoyl}-ethyl)-carbamicacidtert-butylester 

[1]Chemicalandpharmaceuticalbulletin,2002,vol.50,p.239-252

52558-24-4    458531-95-8 

[1]Chemicalandpharmaceuticalbulletin,2002,vol.50,p.239-252

52558-24-4   
Methanesulfonicacid(S)-2-tert-butoxycarbonylamino-1-{(S)-1-(S)-2-(4-methoxy-phenyl)-1-methylcarbamoyl-ethylcarbamoyl-3-methyl-butylcarbamoyl}-ethylester 

[1]Chemicalandpharmaceuticalbulletin,2002,vol.50,p.239-252

21715-90-2    52558-24-4   
C17H22N2O7 

[1]Patent:WO2009/67692,2009,A1.Locationinpatent:Page/Pagecolumn61-62

[2]Patent:WO2009/67692,2009,A1.Locationinpatent:Page/Pagecolumn71

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