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Home Deuterated Building Blocks 60886-80-8
60886-80-8,MFCD00013315
Catalog No.:AA003BF2

60886-80-8 | (1S)-(-)-Camphorsulfonylimine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$14.00   $10.00
- +
25g
98%
in stock  
$64.00   $45.00
- +
  • 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:
AA003BF2
Chemical Name:
(1S)-(-)-Camphorsulfonylimine
CAS Number:
60886-80-8
Molecular Formula:
C10H15NO2S
Molecular Weight:
213.2966
MDL Number:
MFCD00013315
SMILES:
O=S1(=O)N=C2[C@]3(C1)CC[C@H](C2)C3(C)C
Properties
Properties
 
BP:
337.2°C at 760 mmHg  
Form:
Solid  
MP:
236-238°C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
430  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
XLogP3:
1.1  

Upstream Synthesis Route

[1]OrganicLetters,2018,vol.20,#11,p.3286-3290

[2]JournaloftheAmericanChemicalSociety,1938,vol.60,p.2794

[3]SyntheticCommunications,1995,vol.25,#21,p.3323-3327

[4]JournalofOrganicChemistry,2004,vol.69,#26,p.9269-9284

[5]OrganicLetters,2000,vol.2,#26,p.4157-4160

[6]LiebigsAnnalenderChemie,1989,p.739-750

[7]TetrahedronLetters,2013,vol.54,#32,p.4247-4249

[8]OrganicSyntheses,1990,vol.69,p.158-158

[9]BeilsteinJournalofOrganicChemistry,2017,vol.13,p.1230-1238

[1]LiebigsAnnalenderChemie,1989,p.739-750

[2]ChemicalCommunications,1998,#15,p.1549-1550

[3]JournaloftheAmericanChemicalSociety,1988,vol.110,p.8477

[4]OrganicPreparationsandProceduresInternational,2008,vol.40,#2,p.209-213

[5]TetrahedronLetters,2013,vol.54,#32,p.4247-4249

[6]OrganicSyntheses,1990,vol.69,p.158-158

[1]JournalofOrganicChemistry,2004,vol.69,#26,p.9269-9284

[2]OrganicLetters,2000,vol.2,#26,p.4157-4160

[3]JournaloftheAmericanChemicalSociety,1988,vol.110,p.8477

[4]LiebigsAnnalenderChemie,1989,p.739-750

[5]OrganicSyntheses,1990,vol.69,p.158-158

[1]Phosphorus,SulfurandSiliconandtheRelatedElements,2017,vol.192,#5,p.485-489

[1]Patent:US2009/118542,2009,A1,.Locationinpatent:Page/Pagecolumn6

Downstream Synthesis Route

[1]OrganicLetters,2018,vol.20,p.3286-3290

[2]JournaloftheAmericanChemicalSociety,1938,vol.60,p.2794

[3]SyntheticCommunications,1995,vol.25,p.3323-3327

[4]JournalofOrganicChemistry,2004,vol.69,p.9269-9284

[5]OrganicLetters,2000,vol.2,p.4157-4160

[6]LiebigsAnnalenderChemie,1989,p.739-750

[7]TetrahedronLetters,2013,vol.54,p.4247-4249

[8]OrganicSyntheses,1990,vol.69,p.158-158

[9]BeilsteinJournalofOrganicChemistry,2017,vol.13,p.1230-1238

[1]TetrahedronLetters,1988,vol.29,p.6087-6090

[1]LiebigsAnnalenderChemie,1989,p.739-750

[2]ChemicalCommunications,1998,p.1549-1550

[3]JournaloftheAmericanChemicalSociety,1988,vol.110,p.8477

[4]OrganicPreparationsandProceduresInternational,2008,vol.40,p.209-213

[5]TetrahedronLetters,2013,vol.54,p.4247-4249

[6]OrganicSyntheses,1990,vol.69,p.158-158

[1]TetrahedronLetters,1992,vol.33,p.161-164

[2]JournalofOrganicChemistry,1992,vol.57,p.7274-7285

[3]JournalofOrganicChemistry,1990,vol.55,p.3715-3717

[4]OrganicSyntheses,1996,vol.73,p.159-159

[1]JournaloftheChemicalSociety.PerkintransactionsI,1988,p.1753-1758

[2]JournalofOrganicChemistry,1991,vol.56,p.1143-1145

[3]TetrahedronLetters,2010,vol.51,p.6871-6873

[4]BeilsteinJournalofOrganicChemistry,2017,vol.13,p.1230-1238

[5]OrganicSyntheses,1996,vol.73,p.159-159

Literature
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