36016-38-3,MFCD00002107
Catalog No.:AA0035KL

36016-38-3 | tert-Butyl N-hydroxycarbamate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
98%
in stock  
$8.00   $5.00
- +
25g
98%
in stock  
$9.00   $6.00
- +
100g
98%
in stock  
$23.00   $16.00
- +
500g
95%
in stock  
$101.00   $71.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0035KL
Chemical Name:
tert-Butyl N-hydroxycarbamate
CAS Number:
36016-38-3
Molecular Formula:
C5H11NO3
Molecular Weight:
133.1457
MDL Number:
MFCD00002107
SMILES:
ONC(=O)OC(C)(C)C
Properties
Properties
 
BP:
250.4°C at 760 mmHg  
Form:
Solid  
MP:
53-55 °C(lit.)  
Refractive Index:
1.4120 (estimate)  
Stability:
Moisture Sensitive  
Storage:
Inert atmosphere;2-8℃;Keep in dry area;  

Computed Properties
 
Complexity:
105  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.4  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,2018,vol.83,#15,p.8233-8240

[1]Tetrahedron,2003,vol.59,#4,p.543-553

[2]OrganicLetters,2015,vol.17,#6,p.1513-1516

[3]Synthesis(Germany),2016,vol.48,#18,p.3031-3041

[4]BioorganicandMedicinalChemistryLetters,2006,vol.16,#4,p.978-983

[5]Tetrahedron,2004,vol.60,#11,p.2559-2567

[6]Patent:WO2004/13077,2004,A2,.Locationinpatent:Page39

[7]TetrahedronLetters,1999,vol.40,#17,p.3461-3464

[8]Synthesis,2000,#12,p.1719-1726

[9]Patent:WO2011/159177,2011,A1,.Locationinpatent:Page/Pagecolumn41-42

[10]OrganicandBiomolecularChemistry,2009,vol.7,#21,p.4531-4538

[11]JournalofOrganicChemistry,2018,vol.83,#15,p.8233-8240

[12]Patent:WO2004/108677,2004,A1,.Locationinpatent:Page96-97

[13]Tetrahedron,2009,vol.65,#29-30,p.5805-5816

[14]TetrahedronLetters,1996,vol.37,#22,p.3799-3802

[15]Patent:WO2013/155338,2013,A2,.Locationinpatent:Page/Pagecolumn143

[16]Patent:US2015/329503,2015,A1,.Locationinpatent:Paragraph0643;0644

[17]TetrahedronLetters,2005,vol.46,#9,p.1451-1453

[18]OrganicLetters,2012,vol.14,#2,p.656-659

[19]AngewandteChemie-InternationalEdition,2012,vol.51,#29,p.7318-7322

[20]Patent:US2003/130273,2003,A1,

[21]Patent:US2003/130273,2003,A1,

[22]AngewandteChemie-InternationalEdition,2005,vol.44,#1,p.91-96

[23]Patent:US5300503,1994,A,

[24]OrganicLetters,2009,vol.11,#13,p.2828-2831

[25]JournalofAgriculturalandFoodChemistry,2008,vol.56,#23,p.11376-11391

[26]BioorganicandMedicinalChemistryLetters,2010,vol.20,#15,p.4693-4699

[27]JournalofOrganicChemistry,2011,vol.76,#2,p.358-372

[28]ChemicalCommunications,2011,vol.47,#10,p.2853-2855

[29]Synlett,2011,#14,p.1993-1996

[30]Patent:WO2013/92739,2013,A1,.Locationinpatent:Page/Pagecolumn13;14

[31]Chemistry-AEuropeanJournal,2014,vol.20,#3,p.794-800

[32]BioorganicandMedicinalChemistry,2015,vol.23,#1,p.192-202

[33]JournaloftheAmericanChemicalSociety,2014,vol.136,#38,p.13186-13189

[34]OrganicLetters,2016,vol.18,#21,p.5560-5563

[35]JournalofOrganicChemistry,2017,vol.82,#15,p.8251-8257

[36]Patent:CN103936635,2016,B,.Locationinpatent:Paragraph0332;0333

[37]OrganicandBiomolecularChemistry,2018,vol.16,#14,p.2421-2426

[1]JournalofOrganicChemistry,1986,vol.51,#2,p.167-174

[2]JournaloftheAmericanChemicalSociety,1959,vol.81,p.955

[3]JournalofOrganicChemistry,1972,vol.37,p.3520-3523

[1]Tetrahedron,1998,vol.54,#28,p.8217-8222

[2]JournaloftheAmericanChemicalSociety,2015,vol.137,#2,p.568-571

[3]OrganicLetters,2013,vol.15,#2,p.358-361

[1]JournalofMedicinalChemistry,2010,vol.53,#21,p.7731-7738

Downstream Synthesis Route

[1]JournaloftheChemicalSociety.PerkintransactionsI,1980,p.2781-2786

[2]ComptesRendusdesSeancesdel'AcademiedesSciences,SerieC:SciencesChimiques,1975,vol.281,p.789-792

[1]OrganicLetters,2013,vol.15,p.3014-3017

[2]JournalofOrganicChemistry,1972,vol.37,p.3520-3523

[3]OrganicLetters,2007,vol.9,p.3821-3824

[4]Patent:US2006/3967,2006,A1.Locationinpatent:Page/Pagecolumn6-7

[5]Patent:WO2013/92739,2013,A1.Locationinpatent:Page/Pagecolumn14

[6]OrganicLetters,2014,vol.16,p.3328-3331

[7]Chemistry-AEuropeanJournal,2017,vol.23,p.563-567

[1]ComptesRendusdesSeancesdel'AcademiedesSciences,SerieC:SciencesChimiques,1975,vol.281,p.789-792

[1]ComptesRendusdesSeancesdel'AcademiedesSciences,SerieC:SciencesChimiques,1975,vol.281,p.789-792

629-09-4    36016-38-3   
tert-butyl((6-iodohexyl)oxy)carbamate 

[1]TetrahedronLetters,2000,vol.41,p.1531-1533

[2]AngewandteChemie-InternationalEdition,2018,vol.57,p.1532-1536    Angew.Chem.,2018,vol.130,p.1548-1552,5

[3]TetrahedronLetters,2012,vol.53,p.5475-5478

Literature

Title: tert-Butyl (phenylsulfonyl)alkyl-N-hydroxycarbamates: the first class of N-(Boc) nitrone equivalents.

Journal: Organic letters 20051110

Title: Direct evidence for a ruthenium(IV) oxo complex-mediated oxidation of a hydroxamic acid in the presence of phosphine oxide donors.

Journal: Chemical communications (Cambridge, England) 20010921

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SDS
Related Products of 36016-38-3
Tags:36016-38-3 Molecular Formula|36016-38-3 MDL|36016-38-3 SMILES|36016-38-3 tert-Butyl N-hydroxycarbamate
Catalog No.: AA0035KL
36016-38-3,MFCD00002107
36016-38-3 | tert-Butyl N-hydroxycarbamate
Pack Size: 10g
Purity: 98%
in stock
$8.00 $5.00
Pack Size: 25g
Purity: 98%
in stock
$9.00 $6.00
Pack Size: 100g
Purity: 98%
in stock
$23.00 $16.00
Pack Size: 500g
Purity: 95%
in stock
$101.00 $71.00
Quantity
- +
Add to Card
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Technical Information
Catalog Number: AA0035KL
Chemical Name: tert-Butyl N-hydroxycarbamate
CAS Number: 36016-38-3
Molecular Formula: C5H11NO3
Molecular Weight: 133.1457
MDL Number: MFCD00002107
SMILES: ONC(=O)OC(C)(C)C
Properties
BP: 250.4°C at 760 mmHg  
Form: Solid  
MP: 53-55 °C(lit.)  
Refractive Index: 1.4120 (estimate)  
Stability: Moisture Sensitive  
Storage: Inert atmosphere;2-8℃;Keep in dry area;  
Complexity: 105  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.4  
Upstream Synthesis Route
36016-38-3    56267-50-6 

[1]JournalofOrganicChemistry,2018,vol.83,#15,p.8233-8240

24424-99-5    36016-38-3 

[1]Tetrahedron,2003,vol.59,#4,p.543-553

[2]OrganicLetters,2015,vol.17,#6,p.1513-1516

[3]Synthesis(Germany),2016,vol.48,#18,p.3031-3041

[4]BioorganicandMedicinalChemistryLetters,2006,vol.16,#4,p.978-983

[5]Tetrahedron,2004,vol.60,#11,p.2559-2567

[6]Patent:WO2004/13077,2004,A2,.Locationinpatent:Page39

[7]TetrahedronLetters,1999,vol.40,#17,p.3461-3464

[8]Synthesis,2000,#12,p.1719-1726

[9]Patent:WO2011/159177,2011,A1,.Locationinpatent:Page/Pagecolumn41-42

[10]OrganicandBiomolecularChemistry,2009,vol.7,#21,p.4531-4538

[11]JournalofOrganicChemistry,2018,vol.83,#15,p.8233-8240

[12]Patent:WO2004/108677,2004,A1,.Locationinpatent:Page96-97

[13]Tetrahedron,2009,vol.65,#29-30,p.5805-5816

[14]TetrahedronLetters,1996,vol.37,#22,p.3799-3802

[15]Patent:WO2013/155338,2013,A2,.Locationinpatent:Page/Pagecolumn143

[16]Patent:US2015/329503,2015,A1,.Locationinpatent:Paragraph0643;0644

[17]TetrahedronLetters,2005,vol.46,#9,p.1451-1453

[18]OrganicLetters,2012,vol.14,#2,p.656-659

[19]AngewandteChemie-InternationalEdition,2012,vol.51,#29,p.7318-7322

[20]Patent:US2003/130273,2003,A1,

[21]Patent:US2003/130273,2003,A1,

[22]AngewandteChemie-InternationalEdition,2005,vol.44,#1,p.91-96

[23]Patent:US5300503,1994,A,

[24]OrganicLetters,2009,vol.11,#13,p.2828-2831

[25]JournalofAgriculturalandFoodChemistry,2008,vol.56,#23,p.11376-11391

[26]BioorganicandMedicinalChemistryLetters,2010,vol.20,#15,p.4693-4699

[27]JournalofOrganicChemistry,2011,vol.76,#2,p.358-372

[28]ChemicalCommunications,2011,vol.47,#10,p.2853-2855

[29]Synlett,2011,#14,p.1993-1996

[30]Patent:WO2013/92739,2013,A1,.Locationinpatent:Page/Pagecolumn13;14

[31]Chemistry-AEuropeanJournal,2014,vol.20,#3,p.794-800

[32]BioorganicandMedicinalChemistry,2015,vol.23,#1,p.192-202

[33]JournaloftheAmericanChemicalSociety,2014,vol.136,#38,p.13186-13189

[34]OrganicLetters,2016,vol.18,#21,p.5560-5563

[35]JournalofOrganicChemistry,2017,vol.82,#15,p.8251-8257

[36]Patent:CN103936635,2016,B,.Locationinpatent:Paragraph0332;0333

[37]OrganicandBiomolecularChemistry,2018,vol.16,#14,p.2421-2426

1070-19-5    36016-38-3 

[1]JournalofOrganicChemistry,1986,vol.51,#2,p.167-174

[2]JournaloftheAmericanChemicalSociety,1959,vol.81,p.955

[3]JournalofOrganicChemistry,1972,vol.37,p.3520-3523

24424-99-5    5470-11-1    36016-38-3 

[1]Tetrahedron,1998,vol.54,#28,p.8217-8222

[2]JournaloftheAmericanChemicalSociety,2015,vol.137,#2,p.568-571

[3]OrganicLetters,2013,vol.15,#2,p.358-361

24424-95-1    36016-38-3 

[1]JournalofMedicinalChemistry,2010,vol.53,#21,p.7731-7738

Downstream Synthesis Route
36016-38-3    1483-73-4    58377-40-5 

[1]JournaloftheChemicalSociety.PerkintransactionsI,1980,p.2781-2786

[2]ComptesRendusdesSeancesdel'AcademiedesSciences,SerieC:SciencesChimiques,1975,vol.281,p.789-792

36016-38-3    122-04-3    35657-41-1 

[1]OrganicLetters,2013,vol.15,p.3014-3017

[2]JournalofOrganicChemistry,1972,vol.37,p.3520-3523

[3]OrganicLetters,2007,vol.9,p.3821-3824

[4]Patent:US2006/3967,2006,A1.Locationinpatent:Page/Pagecolumn6-7

[5]Patent:WO2013/92739,2013,A1.Locationinpatent:Page/Pagecolumn14

[6]OrganicLetters,2014,vol.16,p.3328-3331

[7]Chemistry-AEuropeanJournal,2017,vol.23,p.563-567

36016-38-3    74-88-4    19689-97-5 

[1]ComptesRendusdesSeancesdel'AcademiedesSciences,SerieC:SciencesChimiques,1975,vol.281,p.789-792

36016-38-3    74-88-4    58377-44-9 

[1]ComptesRendusdesSeancesdel'AcademiedesSciences,SerieC:SciencesChimiques,1975,vol.281,p.789-792

629-09-4    36016-38-3   
tert-butyl((6-iodohexyl)oxy)carbamate 

[1]TetrahedronLetters,2000,vol.41,p.1531-1533

[2]AngewandteChemie-InternationalEdition,2018,vol.57,p.1532-1536    Angew.Chem.,2018,vol.130,p.1548-1552,5

[3]TetrahedronLetters,2012,vol.53,p.5475-5478

Literature fold

Title: tert-Butyl (phenylsulfonyl)alkyl-N-hydroxycarbamates: the first class of N-(Boc) nitrone equivalents.

Journal: Organic letters20051110

Title: Direct evidence for a ruthenium(IV) oxo complex-mediated oxidation of a hydroxamic acid in the presence of phosphine oxide donors.

Journal: Chemical communications (Cambridge, England)20010921

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