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Home Deuterated Building Blocks 170384-29-9
170384-29-9,MFCD10698678
Catalog No.:AA0037V5

170384-29-9 | (2-Oxopropyl)carbamic acid tert-butyl ester

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$6.00   $4.00
- +
250mg
97%
in stock  
$7.00   $5.00
- +
1g
97%
in stock  
$9.00   $6.00
- +
5g
97%
in stock  
$19.00   $13.00
- +
10g
97%
in stock  
$29.00   $20.00
- +
25g
97%
in stock  
$63.00   $44.00
- +
100g
97%
in stock  
$189.00   $132.00
- +
  • 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:
AA0037V5
Chemical Name:
(2-Oxopropyl)carbamic acid tert-butyl ester
CAS Number:
170384-29-9
Molecular Formula:
C8H15NO3
Molecular Weight:
173.2096
MDL Number:
MFCD10698678
SMILES:
CC(=O)CNC(=O)OC(C)(C)C
NSC Number:
617629
Properties
Computed Properties
 
Complexity:
181  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
0.7  

Upstream Synthesis Route

[1]Patent:US2006/4046,2006,A1,.Locationinpatent:Page/Pagecolumn22

[1]OrganicLetters,2011,vol.13,#11,p.2932-2935

[2]JournaloftheChemicalSociety.PerkinTransactions1,2001,#16,p.1916-1928

[3]RussianChemicalBulletin,2005,vol.54,#6,p.1535-1536

[4]Synthesis(Germany),2015,vol.47,#18,p.2756-2766

[5]Patent:WO2006/104356,2006,A1,.Locationinpatent:Page/Pagecolumn27

[6]HelveticaChimicaActa,1980,vol.63,#7,p.1915-1919

[7]Synthesis,2006,#6,p.952-958

[1]TetrahedronLetters,2002,vol.43,#46,p.8223-8226

[2]Patent:US2006/4046,2006,A1,.Locationinpatent:Page/Pagecolumn22

[3]HelveticaChimicaActa,1995,vol.78,#3,p.703-714

[1]BioorganicandMedicinalChemistryLetters,2018,vol.28,#12,p.2180-2183

[1]JournalofOrganicChemistry,1996,vol.61,#15,p.4999-5003

[2]JournalofOrganicChemistry,2009,vol.74,#5,p.1932-1938

Downstream Synthesis Route

[1]HelveticaChimicaActa,1980,vol.63,p.1915-1919

[1]OrganicLetters,2011,vol.13,p.2932-2935

[2]JournaloftheChemicalSociety.PerkinTransactions1(2001),2001,p.1916-1928

[3]RussianChemicalBulletin,2005,vol.54,p.1535-1536

[4]Synthesis,2015,vol.47,p.2756-2766

[5]Patent:WO2006/104356,2006,A1.Locationinpatent:Page/Pagecolumn27

[6]HelveticaChimicaActa,1980,vol.63,p.1915-1919

[7]Synthesis,2006,p.952-958

[1]TetrahedronLetters,2002,vol.43,p.8223-8226

[2]Patent:US2006/4046,2006,A1.Locationinpatent:Page/Pagecolumn22

[3]HelveticaChimicaActa,1995,vol.78,p.703-714

506-87-6    170384-29-9   
rac-tert-butyl<(4-methyl-2,5-dioxoimidazolidin-4-yl)methyl>carbamate 

[1]HelveticaChimicaActa,1995,vol.78,p.703-714

4746-97-8    170384-29-9   
2-Hydroxy-2-(8-oxo-1,4-dioxa-spiro4.5dec-7-yl)-propyl-carbamicacidtert-butylester 

[1]JournalofOrganicChemistry,1996,vol.61,p.4999-5003

Literature
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SDS
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