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Home Amines 177906-48-8
177906-48-8,MFCD03001719
Catalog No.:AA0037LP

177906-48-8 | N-Boc-trans-1,4-cyclohexanediamine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
500mg
97%
in stock  
$3.00   $2.00
- +
5g
95%
in stock  
$23.00   $16.00
- +
10g
95%
in stock  
$23.00   $16.00
- +
25g
95%
in stock  
$48.00   $34.00
- +
100g
95%
in stock  
$183.00   $128.00
- +
500g
95%
in stock  
$913.00   $639.00
- +
  • 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:
AA0037LP
Chemical Name:
N-Boc-trans-1,4-cyclohexanediamine
CAS Number:
177906-48-8
Molecular Formula:
C11H22N2O2
Molecular Weight:
214.3046
MDL Number:
MFCD03001719
SMILES:
N[C@@H]1CC[C@H](CC1)NC(=O)OC(C)(C)C
Properties
Properties
 
BP:
322°C at 760 mmHg  
Form:
Solid  
MP:
74.5 - 75.5 °C  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
215  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
1.3  

Upstream Synthesis Route

[1]Chemistry-AnAsianJournal,2010,vol.5,#4,p.877-886

[2]Patent:WO2016/160617,2016,A2,.Locationinpatent:Paragraph00401

[3]JournalofOrganicChemistry,1996,vol.61,#25,p.8811-8818

[4]Patent:WO2016/116563,2016,A1,.Locationinpatent:Page/Pagecolumn34-35

[5]Patent:WO2008/57468,2008,A1,.Locationinpatent:Page/Pagecolumn352

[6]Patent:WO2013/134079,2013,A1,.Locationinpatent:Paragraph0176-0177

[7]BioorganicandMedicinalChemistry,2000,vol.8,#6,p.1451-1466

[8]BioorganicandMedicinalChemistryLetters,2004,vol.14,#20,p.5223-5226

[9]Patent:KR2015/83721,2015,A,.Locationinpatent:Page/Pagecolumn18

[10]ChemicalCommunications,2017,vol.53,#6,p.1064-1067

[11]JournalofEnzymeInhibitionandMedicinalChemistry,2017,vol.32,#1,p.865-877

[12]EuropeanJournalofMedicinalChemistry,2018,vol.150,p.655-666

[13]Patent:EP1323710,2003,A1,

[1]Phytochemistry,2003,vol.63,#3,p.315-334

[1]Patent:EP1775298,2007,A1,.Locationinpatent:Page/Pagecolumn33-34

Downstream Synthesis Route

[1]Chemistry-AnAsianJournal,2010,vol.5,p.877-886

[2]Patent:US2020/39979,2020,A1.Locationinpatent:Paragraph0417-0418

[3]Patent:CN110894209,2020,A.Locationinpatent:Paragraph0085;0202;0205;0214

[4]Patent:WO2016/160617,2016,A2.Locationinpatent:Paragraph00401

[5]JournalofOrganicChemistry,1996,vol.61,p.8811-8818

[6]Patent:WO2016/116563,2016,A1.Locationinpatent:Page/Pagecolumn34-35

[7]Patent:WO2008/57468,2008,A1.Locationinpatent:Page/Pagecolumn352

[8]Patent:CN109988172,2019,A.Locationinpatent:Paragraph0030

[9]Patent:WO2013/134079,2013,A1.Locationinpatent:Paragraph0176-0177

[10]BioorganicandMedicinalChemistry,2000,vol.8,p.1451-1466

[11]BioorganicandMedicinalChemistry,2019,vol.27,p.383-393

[12]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.5223-5226

[13]Patent:KR2015/83721,2015,A.Locationinpatent:Page/Pagecolumn18

[14]ChemicalCommunications,2017,vol.53,p.1064-1067

[15]JournalofEnzymeInhibitionandMedicinalChemistry,2017,vol.32,p.865-877

[16]EuropeanJournalofMedicinalChemistry,2018,vol.150,p.655-666

[17]Patent:EP1323710,2003,A1

779-27-1    177906-48-8   
C21H26N2O6 

[1]JournaloftheAmericanChemicalSociety,2007,vol.129,p.10616-10617

[1]Patent:WO2006/20415,2006,A1.Locationinpatent:Page/Pagecolumn105

177906-48-8    7115-91-5   
N-tert-butoxycarbonyl-trans-4-(1-oxo-2-isoindolinyl)cyclohexylamine 

[1]CurrentPatentAssignee:MITSUBISHICHEMICALHOLDINGSCORPORATION-EP1323710,2003,A1

[1]Patent:EP1775298,2007,A1.Locationinpatent:Page/Pagecolumn33-34

Literature
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Additional Info:
SDS
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