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Home Bromides 158407-04-6
158407-04-6,MFCD04115538
Catalog No.:AA001Q3A

158407-04-6 | tert-Butyl 4-(bromomethyl)piperidine-1-carboxylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$6.00   $4.00
- +
250mg
97%
in stock  
$13.00   $9.00
- +
1g
95%
in stock  
$18.00   $13.00
- +
5g
95%
in stock  
$23.00   $16.00
- +
10g
97%
in stock  
$31.00   $22.00
- +
25g
97%
in stock  
$74.00   $52.00
- +
100g
97%
in stock  
$294.00   $206.00
- +
  • 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:
AA001Q3A
Chemical Name:
tert-Butyl 4-(bromomethyl)piperidine-1-carboxylate
CAS Number:
158407-04-6
Molecular Formula:
C11H20BrNO2
Molecular Weight:
278.1860
MDL Number:
MFCD04115538
SMILES:
BrCC1CCN(CC1)C(=O)OC(C)(C)C
Properties
Properties
 
BP:
318.3°C at 760 mmHg  
Form:
Solid  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
217  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
2.6  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,2008,vol.51,#17,p.5176-5197

[1]Patent:WO2016/75661,2016,A1,.Locationinpatent:Page/Pagecolumn30

[2]Patent:WO2006/50506,2006,A1,.Locationinpatent:Page/Pagecolumn120-121

[3]RSCAdvances,2016,vol.6,#52,p.46170-46185

[4]Patent:WO2017/27684,2017,A1,.Locationinpatent:Paragraph00266

[5]BioorganicandMedicinalChemistryLetters,1999,vol.9,#17,p.2615-2620

[6]Patent:WO2006/46031,2006,A1,.Locationinpatent:Page/Pagecolumn82

[7]Patent:US2008/76758,2008,A1,.Locationinpatent:Page/Pagecolumn95-96

[8]Patent:US2004/77646,2004,A1,.Locationinpatent:Page130

[9]Patent:WO2013/80141,2013,A1,.Locationinpatent:Page/Pagecolumn139

[10]Patent:WO2013/190123,2013,A1,.Locationinpatent:Page/Pagecolumn129;130

[11]BioorganicandMedicinalChemistryLetters,2015,vol.25,#6,p.1318-1323

[12]Patent:US2015/183804,2015,A1,.Locationinpatent:Paragraph1080;1081;1082;1083;1084

[13]EuropeanJournalofMedicinalChemistry,2018,vol.145,p.96-112

[1]EuropeanJournalofMedicinalChemistry,2018,vol.145,p.96-112

[1]BioorganicandMedicinalChemistryLetters,1999,vol.9,#17,p.2615-2620

Downstream Synthesis Route

[1]Patent:WO2016/75661,2016,A1.Locationinpatent:Page/Pagecolumn30

[2]Patent:WO2006/50506,2006,A1.Locationinpatent:Page/Pagecolumn120-121

[3]RSCAdvances,2016,vol.6,p.46170-46185

[4]OrganicLetters,2020,vol.22,p.4000-4005

[5]Patent:WO2017/27684,2017,A1.Locationinpatent:Paragraph00266

[6]BioorganicandMedicinalChemistryLetters,1999,vol.9,p.2615-2620

[7]Patent:WO2006/46031,2006,A1.Locationinpatent:Page/Pagecolumn82

[8]Patent:US2008/76758,2008,A1.Locationinpatent:Page/Pagecolumn95-96

[9]Patent:US2004/77646,2004,A1.Locationinpatent:Page130

[10]Patent:WO2013/80141,2013,A1.Locationinpatent:Page/Pagecolumn139

[11]Patent:WO2013/190123,2013,A1.Locationinpatent:Page/Pagecolumn129;130

[12]BioorganicandMedicinalChemistryLetters,2015,vol.25,p.1318-1323

[13]Patent:US2015/183804,2015,A1.Locationinpatent:Paragraph1080;1081;1082;1083;1084

[14]EuropeanJournalofMedicinalChemistry,2018,vol.145,p.96-112

[15]Patent:CN109970740,2019,A

[1]Patent:WO2008/133955,2008,A1.Locationinpatent:Page/Pagecolumn114

[1]JournalofMedicinalChemistry,2008,vol.51,p.5176-5197

[1]JournalofMedicinalChemistry,2016,vol.59,p.5221-5237

[2]Patent:WO2009/44162,2009,A1.Locationinpatent:Page/Pagecolumn237

[1]Patent:WO2010/80864,2010,A1.Locationinpatent:Page/Pagecolumn134

Literature
Quotation Request
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Additional Info:
SDS
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