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136027-17-3,MFCD28098092
Catalog No.:AA009JMW

136027-17-3 | (2-Sulfamoyl-ethyl)-carbamic acid benzyl ester

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Purity
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250mg
98%
in stock  
$7.00   $5.00
- +
1g
98%
in stock  
$9.00   $7.00
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5g
98%
in stock  
$22.00   $15.00
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  • 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:
AA009JMW
Chemical Name:
(2-Sulfamoyl-ethyl)-carbamic acid benzyl ester
CAS Number:
136027-17-3
Molecular Formula:
C10H14N2O4S
Molecular Weight:
258.2942
MDL Number:
MFCD28098092
SMILES:
O=C(NCCS(=O)(=O)N)OCc1ccccc1
Properties
Computed Properties
 
Complexity:
331  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
6  
XLogP3:
0.1  

Upstream Synthesis Route

[1]Patent:CN106008283,2016,A,.Locationinpatent:Paragraph0028;0029;0030

[2]Patent:EP2484678,2012,A1,.Locationinpatent:Page/Pagecolumn14

[3]Patent:US2012/208833,2012,A1,.Locationinpatent:Page/Pagecolumn10

[4]AminoAcids,2012,vol.43,#1,p.423-429

[5]JournaloftheAmericanChemicalSociety,2006,vol.128,#6,p.1995-2004

[6]Synthesis,2006,#3,p.455-460

[7]Patent:US2003/216392,2003,A1,

[8]OrganicLetters,2009,vol.11,#17,p.3922-3925

[9]ScienceChinaChemistry,2012,vol.55,#12,p.2548-2553

[10]Synthesis(Germany),2015,vol.47,#20,p.3186-3190

[11]Patent:WO2017/60874,2017,A1,.Locationinpatent:Paragraph00700;00724

[1]JournaloftheAmericanChemicalSociety,2006,vol.128,#6,p.1995-2004

[2]Patent:EP2484678,2012,A1,

[3]Patent:US2012/208833,2012,A1,

[4]Patent:US2013/237700,2013,A1,.Locationinpatent:Paragraph0026

[1]Synthesis,2006,#3,p.455-460

[2]JournalofPeptideScience,2010,vol.16,#1,p.1-5

[1]Synthesis,2006,#3,p.455-460

[2]JournaloftheAmericanChemicalSociety,2006,vol.128,#6,p.1995-2004

[3]AminoAcids,2012,vol.43,#1,p.423-429

[4]Patent:EP2484678,2012,A1,

[5]Patent:US2012/208833,2012,A1,

[6]ScienceChinaChemistry,2012,vol.55,#12,p.2548-2553

[7]Patent:CN106008283,2016,A,

[1]JournalofOrganicChemistry,2014,vol.79,#6,p.2688-2693

Downstream Synthesis Route

[1]JournaloftheChemicalSociety,1941,p.76

[2]JournaloftheAmericanChemicalSociety,2006,vol.128,p.1995-2004

sodium-saltof/the/2-benzyloxycarbonylamino-ethane-sulfonicacid-(1) 
  136027-17-3 

[1]JournaloftheChemicalSociety,1941,p.76

[1]Synthesis,2006,p.455-460

[2]JournalofPeptideScience,2010,vol.16,p.1-5

[1]Patent:CN106008283,2016,A.Locationinpatent:Paragraph0028;0029;0030

[2]Patent:EP2484678,2012,A1.Locationinpatent:Page/Pagecolumn14

[3]Patent:US2012/208833,2012,A1.Locationinpatent:Page/Pagecolumn10

[4]AminoAcids,2012,vol.43,p.423-429

[5]JournaloftheAmericanChemicalSociety,2006,vol.128,p.1995-2004

[6]Synthesis,2006,p.455-460

[7]Patent:US2003/216392,2003,A1

[8]OrganicLetters,2009,vol.11,p.3922-3925

[9]ScienceChinaChemistry,2012,vol.55,p.2548-2553

[10]Synthesis,2015,vol.47,p.3186-3190

[11]Patent:WO2017/60874,2017,A1.Locationinpatent:Paragraph00700;00724

[1]Synthesis,2006,p.455-460

[2]AminoAcids,2012,vol.43,p.423-429

Literature
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SDS
Tags:136027-17-3 Molecular Formula|136027-17-3 MDL|136027-17-3 SMILES|136027-17-3 (2-Sulfamoyl-ethyl)-carbamic acid benzyl ester