+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
72080-83-2,MFCD02094510
Catalog No.:AA008QVF

72080-83-2 | Benzyl 2-aminoethylcarbamate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$12.00   $8.00
- +
5g
97%
in stock  
$26.00   $18.00
- +
25g
95%
in stock  
$108.00   $76.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA008QVF
Chemical Name:
Benzyl 2-aminoethylcarbamate
CAS Number:
72080-83-2
Molecular Formula:
C10H14N2O2
Molecular Weight:
194.2304
MDL Number:
MFCD02094510
SMILES:
NCCNC(=O)OCc1ccccc1
Properties
Computed Properties
 
Complexity:
168  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.7  

Upstream Synthesis Route

[1]ChemicalCommunications,2017,vol.53,#52,p.7088-7091

[2]NewJournalofChemistry,2013,vol.37,#7,p.1895-1905

[3]ACSMedicinalChemistryLetters,2014,vol.5,#5,p.550-555

[4]Chemistry-AEuropeanJournal,2011,vol.17,#19,p.5251-5255

[5]Synthesis,1984,#12,p.1032-1033

[6]Patent:CN104557704,2017,B,.Locationinpatent:Paragraph0052;0053;0054

[7]AngewandteChemie,InternationalEdition,2012,vol.51,#40,p.10060-10063,4

[8]AngewandteChemie,2012,vol.124,#40,p.10207-10210,4

[9]AngewandteChemie-InternationalEdition,2012,vol.51,#40,p.10060-10063

[10]Angew.Chem.,2012,vol.124,#40,p.10207-10210,4

[11]HelveticaChimicaActa,1982,vol.65,#6,p.1853-1867

[12]ChemistryLetters,2007,vol.36,#10,p.1220-1221

[13]RussianJournalofBioorganicChemistry,1994,vol.20,#7,p.397-405

[14]BioorganicheskayaKhimiya,1994,vol.20,#7,p.740-750

[15]JournalofOrganicChemistry,2007,vol.72,#22,p.8280-8289

[16]Patent:WO2013/124286,2013,A1,.Locationinpatent:Page/Pagecolumn65

[17]Patent:US2018/99940,2018,A1,.Locationinpatent:Paragraph0658-0664

[18]Patent:CN103450164,2017,B,.Locationinpatent:Paragraph0049;0053;0054

[1]BulletinoftheKoreanChemicalSociety,2010,vol.31,#10,p.2854-2860

[2]MedicinalChemistryResearch,2016,vol.25,#5,p.824-833

[3]JournalofChemicalResearch,Miniprint,1992,#12,p.3117-3132

[4]EuropeanJournalofMedicinalChemistry,2011,vol.46,#12,p.5769-5777

[1]Patent:US2010/41748,2010,A1,.Locationinpatent:Page/Pagecolumn115

[1]Patent:WO2015/81282,2015,A1,.Locationinpatent:Paragraph00714;00715

[1]Patent:US2008/318957,2008,A1,.Locationinpatent:Page/Pagecolumn57;58

[2]ChemicalCommunications,2011,vol.47,#33,p.9330-9332

[3]OrganicLetters,2012,vol.14,#17,p.4450-4453

[4]Patent:WO2016/102562,2016,A1,.Locationinpatent:Page/Pagecolumn52

Downstream Synthesis Route

[1]Lawson;LeaferJr.;Tewes;Rao[Hoppe-Seyler'sZeitschriftfurPhysiologischeChemie,1968,vol.349,#2,p.251-262]

[2]Noguchi,J.etal.[IsraelJournalofChemistry,1974,vol.12,p.87-101]

[1]JournalofMedicinalChemistry,1985,vol.28,p.1568-1574

[1]JournalofOrganicChemistry,1981,vol.46,p.2455-2465

[2]TetrahedronLetters,2007,vol.48,p.8318-8322

[3]BulletinoftheChemicalSocietyofJapan,1998,vol.71,p.699-709

[4]JournalofCombinatorialChemistry,2010,vol.12,p.248-254

[1]ChemicalCommunications,2017,vol.53,p.7088-7091

[2]Patent:WO2019/127607,2019,A1.Locationinpatent:Page/Pagecolumn12;217

[3]NewJournalofChemistry,2013,vol.37,p.1895-1905

[4]ACSMedicinalChemistryLetters,2014,vol.5,p.550-555

[5]Chemistry-AEuropeanJournal,2011,vol.17,p.5251-5255

[6]Synthesis,1984,p.1032-1033

[7]Patent:CN104557704,2017,B.Locationinpatent:Paragraph0052;0053;0054

[8]AngewandteChemie-InternationalEdition,2012,vol.51,p.10060-10063,4    AngewandteChemie,2012,vol.124,p.10207-10210,4

[9]HelveticaChimicaActa,1982,vol.65,p.1853-1867

[10]ChemistryLetters,2007,vol.36,p.1220-1221

[11]RussianJournalofBioorganicChemistry,1994,vol.20,p.397-405    BioorganicheskayaKhimiya,1994,vol.20,p.740-750

[12]JournalofOrganicChemistry,2007,vol.72,p.8280-8289

[13]Patent:WO2013/124286,2013,A1.Locationinpatent:Page/Pagecolumn65

[14]Patent:US2018/99940,2018,A1.Locationinpatent:Paragraph0658-0664

[15]Patent:CN103450164,2017,B.Locationinpatent:Paragraph0049;0053;0054

[16]Patent:WO2019/67979,2019,A1.Locationinpatent:Page/Pagecolumn84-85

[1]BulletinoftheKoreanChemicalSociety,2010,vol.31,p.2854-2860

[2]MedicinalChemistryResearch,2016,vol.25,p.824-833

[3]JournalofChemicalResearch,Miniprint,1992,p.3117-3132

[4]EuropeanJournalofMedicinalChemistry,2011,vol.46,p.5769-5777

Literature
Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 72080-83-2
18807-71-1

18807-71-1

 121505-94-0

121505-94-0

 160256-75-7

160256-75-7

 2503-29-9

2503-29-9

 277328-34-4

277328-34-4

 302557-32-0

302557-32-0
Building Blocks
More >
Tags:72080-83-2 Molecular Formula|72080-83-2 MDL|72080-83-2 SMILES|72080-83-2 Benzyl 2-aminoethylcarbamate
Catalog No.: AA008QVF
72080-83-2,MFCD02094510
72080-83-2 | Benzyl 2-aminoethylcarbamate
Pack Size： 1g
Purity： 97%
in stock
$12.00 $8.00
Pack Size： 5g
Purity： 97%
in stock
$26.00 $18.00
Pack Size： 25g
Purity： 95%
in stock
$108.00 $76.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA008QVF
Chemical Name: Benzyl 2-aminoethylcarbamate
CAS Number: 72080-83-2
Molecular Formula: C10H14N2O2
Molecular Weight: 194.2304
MDL Number: MFCD02094510
SMILES: NCCNC(=O)OCc1ccccc1
Properties
Complexity: 168  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.7  
Upstream Synthesis Route
501-53-1    107-15-3    72080-83-2 

[1]ChemicalCommunications,2017,vol.53,#52,p.7088-7091

[2]NewJournalofChemistry,2013,vol.37,#7,p.1895-1905

[3]ACSMedicinalChemistryLetters,2014,vol.5,#5,p.550-555

[4]Chemistry-AEuropeanJournal,2011,vol.17,#19,p.5251-5255

[5]Synthesis,1984,#12,p.1032-1033

[6]Patent:CN104557704,2017,B,.Locationinpatent:Paragraph0052;0053;0054

[7]AngewandteChemie,InternationalEdition,2012,vol.51,#40,p.10060-10063,4

[8]AngewandteChemie,2012,vol.124,#40,p.10207-10210,4

[9]AngewandteChemie-InternationalEdition,2012,vol.51,#40,p.10060-10063

[10]Angew.Chem.,2012,vol.124,#40,p.10207-10210,4

[11]HelveticaChimicaActa,1982,vol.65,#6,p.1853-1867

[12]ChemistryLetters,2007,vol.36,#10,p.1220-1221

[13]RussianJournalofBioorganicChemistry,1994,vol.20,#7,p.397-405

[14]BioorganicheskayaKhimiya,1994,vol.20,#7,p.740-750

[15]JournalofOrganicChemistry,2007,vol.72,#22,p.8280-8289

[16]Patent:WO2013/124286,2013,A1,.Locationinpatent:Page/Pagecolumn65

[17]Patent:US2018/99940,2018,A1,.Locationinpatent:Paragraph0658-0664

[18]Patent:CN103450164,2017,B,.Locationinpatent:Paragraph0049;0053;0054

146552-66-1    72080-83-2 

[1]BulletinoftheKoreanChemicalSociety,2010,vol.31,#10,p.2854-2860

[2]MedicinalChemistryResearch,2016,vol.25,#5,p.824-833

[3]JournalofChemicalResearch,Miniprint,1992,#12,p.3117-3132

[4]EuropeanJournalofMedicinalChemistry,2011,vol.46,#12,p.5769-5777

83019-89-0    501-53-1    72080-83-2 

[1]Patent:US2010/41748,2010,A1,.Locationinpatent:Page/Pagecolumn115

18807-71-1    72080-83-2 

[1]Patent:WO2015/81282,2015,A1,.Locationinpatent:Paragraph00714;00715

13139-17-8    107-15-3    72080-83-2 

[1]Patent:US2008/318957,2008,A1,.Locationinpatent:Page/Pagecolumn57;58

[2]ChemicalCommunications,2011,vol.47,#33,p.9330-9332

[3]OrganicLetters,2012,vol.14,#17,p.4450-4453

[4]Patent:WO2016/102562,2016,A1,.Locationinpatent:Page/Pagecolumn52

Downstream Synthesis Route
18807-67-5    72080-83-2 

[1]Lawson;LeaferJr.;Tewes;Rao[Hoppe-Seyler'sZeitschriftfurPhysiologischeChemie,1968,vol.349,#2,p.251-262]

[2]Noguchi,J.etal.[IsraelJournalofChemistry,1974,vol.12,p.87-101]

75092-39-6    72080-83-2    97614-96-5 

[1]JournalofMedicinalChemistry,1985,vol.28,p.1568-1574

24424-99-5    72080-83-2    77153-05-0 

[1]JournalofOrganicChemistry,1981,vol.46,p.2455-2465

[2]TetrahedronLetters,2007,vol.48,p.8318-8322

[3]BulletinoftheChemicalSocietyofJapan,1998,vol.71,p.699-709

[4]JournalofCombinatorialChemistry,2010,vol.12,p.248-254

501-53-1    107-15-3    72080-83-2 

[1]ChemicalCommunications,2017,vol.53,p.7088-7091

[2]Patent:WO2019/127607,2019,A1.Locationinpatent:Page/Pagecolumn12;217

[3]NewJournalofChemistry,2013,vol.37,p.1895-1905

[4]ACSMedicinalChemistryLetters,2014,vol.5,p.550-555

[5]Chemistry-AEuropeanJournal,2011,vol.17,p.5251-5255

[6]Synthesis,1984,p.1032-1033

[7]Patent:CN104557704,2017,B.Locationinpatent:Paragraph0052;0053;0054

[8]AngewandteChemie-InternationalEdition,2012,vol.51,p.10060-10063,4    AngewandteChemie,2012,vol.124,p.10207-10210,4

[9]HelveticaChimicaActa,1982,vol.65,p.1853-1867

[10]ChemistryLetters,2007,vol.36,p.1220-1221

[11]RussianJournalofBioorganicChemistry,1994,vol.20,p.397-405    BioorganicheskayaKhimiya,1994,vol.20,p.740-750

[12]JournalofOrganicChemistry,2007,vol.72,p.8280-8289

[13]Patent:WO2013/124286,2013,A1.Locationinpatent:Page/Pagecolumn65

[14]Patent:US2018/99940,2018,A1.Locationinpatent:Paragraph0658-0664

[15]Patent:CN103450164,2017,B.Locationinpatent:Paragraph0049;0053;0054

[16]Patent:WO2019/67979,2019,A1.Locationinpatent:Page/Pagecolumn84-85

146552-66-1    72080-83-2 

[1]BulletinoftheKoreanChemicalSociety,2010,vol.31,p.2854-2860

[2]MedicinalChemistryResearch,2016,vol.25,p.824-833

[3]JournalofChemicalResearch,Miniprint,1992,p.3117-3132

[4]EuropeanJournalofMedicinalChemistry,2011,vol.46,p.5769-5777

Related Products of of 72080-83-2
18807-71-1
18807-71-1
121505-94-0
121505-94-0
160256-75-7
160256-75-7
2503-29-9
2503-29-9
277328-34-4
277328-34-4
302557-32-0
302557-32-0
Building Blocks More >
117027-46-0
117027-46-0
BOC-D-3,3-DIPHENYLALANINE
AA008R68 | MFCD00191187
10552-74-6
10552-74-6
NITROTHAL-ISOPROPYL
AA008RI0 | MFCD00055456
113211-36-2
113211-36-2
O-(2-[3-(Trifluoromethyl)phenoxy]ethyl)hydroxylamine HCl
AA008RO4 | MFCD01114594
1002034-26-5
1002034-26-5
1-(Difluoromethyl)-3-nitro-1h-pyrazole
AA008RX5 | MFCD04967410
104774-88-1
104774-88-1
4-(3-Fluoro-phenyl)-piperidine
AA008S4I | MFCD05189920
1045332-30-6
1045332-30-6
4-(Pyridin-4-yl)phenyl boronic acid
AA008SDE | MFCD17170043
104873-71-4
104873-71-4
1,2:4,5-Biscyclohexylidene-DL-myo-inositol
AA008SL3 | MFCD00152059
1110772-09-2
1110772-09-2
(1R,3S)-3-(Aminomethyl)cyclopentanol
AA008SQQ | MFCD11052502
1185318-69-7
1185318-69-7
3-BROMOTOLUENE-D7
AA008SWU | MFCD06658865
10574-37-5
10574-37-5
2,3-DIMETHYL-2-PENTENE
AA008T5O | MFCD00027048
Submit
© 2017 AA BLOCKS, INC. All rights reserved.