15184-96-0,MFCD00035956
Catalog No.:AA003SHL

15184-96-0 | N,N-Dimethyl-4-nitrobenzylamine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$27.00   $19.00
- +
5g
≥95%
in stock  
$44.00   $31.00
- +
10g
95%
in stock  
$56.00   $39.00
- +
25g
95%
in stock  
$136.00   $95.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003SHL
Chemical Name:
N,N-Dimethyl-4-nitrobenzylamine
CAS Number:
15184-96-0
Molecular Formula:
C9H12N2O2
Molecular Weight:
180.2038
MDL Number:
MFCD00035956
SMILES:
CN(Cc1ccc(cc1)[N+](=O)[O-])C
Properties
Properties
 
BP:
262.4°C at 760 mmHg  
Form:
Liquid  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
169  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2  

Upstream Synthesis Route

[1]MedicinalChemistry,2016,vol.12,#5,p.489-498

[2]EuropeanJournalofMedicinalChemistry,2014,vol.86,p.257-269

[3]ArchivderPharmazie,2014,vol.347,#12,p.936-949

[4]Patent:WO2006/123145,2006,A1,.Locationinpatent:Page/Pagecolumn58

[5]JournaloftheAmericanChemicalSociety,1983,vol.105,#13,p.4136-4142

[6]Patent:KR2018/74094,2018,A,.Locationinpatent:Paragraph0098-0101

[7]BioorganicandMedicinalChemistryLetters,2004,vol.14,#9,p.2061-2065

[1]JournaloftheAmericanChemicalSociety,2009,vol.131,#41,p.15032-15040

[2]Chemistry-AEuropeanJournal,2017,vol.23,#9,p.2005-2009

[3]RSCAdvances,2017,vol.7,#80,p.50729-50738

[4]JournaloftheAmericanChemicalSociety,2010,vol.132,#6,p.1770-1771

[5]AngewandteChemie-InternationalEdition,2013,vol.52,#44,p.11577-11580

[6]Angew.Chem.,2013,vol.125,#44,p.11791-11794,4

[7]Chemistry-AEuropeanJournal,2011,vol.17,#43,p.12186-12192

[8]AngewandteChemie-InternationalEdition,2016,vol.55,#42,p.13326-13329

[9]Angew.Chem.,2016,vol.128,#42,p.13520-13523,4

[10]JournaloftheAmericanChemicalSociety,1964,vol.86,p.3566-3567

[11]Synthesis,1981,#12,p.996-997

[12]TetrahedronLetters,1980,vol.21,#42,p.4061-4064

[13]ChemicalCommunications,2016,vol.52,#82,p.12195-12198

[1]SyntheticCommunications,2000,vol.30,#11,p.2001-2008

[2]Patent:WO2008/77885,2008,A2,.Locationinpatent:Page/Pagecolumn19

[1]JournalofMedicinalChemistry,2009,vol.52,#14,p.4466-4480

[2]ChemischeBerichte,1895,vol.28,p.1141

[3]ArchivderPharmazie,1962,vol.295/67,p.690-697

[4]BulletindelaSocieteChimiquedeFrance,1975,p.679-685

[5]JournaloftheChemicalSociety,1929,p.267

[6]JournaloftheChemicalSociety,1927,p.1904

[7]BioorganicandMedicinalChemistryLetters,2008,vol.18,#12,p.3641-3645

[1]JournalofMedicinalChemistry,2013,vol.56,#7,p.2975-2990

[2]Patent:EP2824108,2015,A1,.Locationinpatent:Paragraph0104

[3]Patent:US2015/166595,2015,A1,.Locationinpatent:Paragraph0222

Downstream Synthesis Route
64-18-6   
(4-nitro-benzyl)-hexamethylenetetraminium;chloride 
  15184-96-0 

[1]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1922,vol.174,p.689

3-chloro-propionicaciddodecylamide 
  15184-96-0   
(2-dodecylcarbamoyl-ethyl)-dimethyl-(4-nitro-benzyl)-ammonium;chloride 

[1]Patent:US2317999,1940,

[1]RSCAdvances,2015,vol.5,p.47125-47130

[2]JournalofMedicinalChemistry,2013,vol.56,p.2975-2990

[3]Patent:WO2006/123145,2006,A1.Locationinpatent:Page/Pagecolumn58

[4]EuropeanJournalofMedicinalChemistry,2014,vol.86,p.257-269

[5]ArchivderPharmazie,2014,vol.347,p.936-949

[6]MedicinalChemistry,2016,vol.12,p.489-498

[7]Patent:CN109265453,2019,A.Locationinpatent:Paragraph0081;0087-0089

[8]Patent:KR2018/74094,2018,A.Locationinpatent:Paragraph0104-0109

[9]CollectionofCzechoslovakChemicalCommunications,1990,vol.55,p.282-295

[10]JournaloftheChemicalSociety,1935,p.871

[11]JournaloftheChemicalSociety,1927,p.1904

[12]Patent:US6166006,2000,A

[13]Patent:WO2008/77885,2008,A2.Locationinpatent:Page/Pagecolumn19

[14]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.3641-3645

[15]JournalofMedicinalChemistry,2009,vol.52,p.4466-4480

[16]Patent:US2006/58341,2006,A1.Locationinpatent:Page/Pagecolumn30

[17]Patent:EP2824108,2015,A1.Locationinpatent:Paragraph0105

[18]Patent:US2015/166595,2015,A1.Locationinpatent:Paragraph0223

[19]MedChemComm,2019,vol.10,p.465-477

[20]ChemicalandPharmaceuticalBulletin,2019,vol.67,p.351-360

[1]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1922,vol.174,p.689

[1]JournaloftheAmericanChemicalSociety,2009,vol.131,p.15032-15040

[2]Chemistry-AEuropeanJournal,2017,vol.23,p.2005-2009

[3]RSCAdvances,2017,vol.7,p.50729-50738

[4]JournaloftheAmericanChemicalSociety,2010,vol.132,p.1770-1771

[5]AngewandteChemie-InternationalEdition,2013,vol.52,p.11577-11580    Angew.Chem.,2013,vol.125,p.11791-11794,4

[6]Chemistry-AEuropeanJournal,2011,vol.17,p.12186-12192

[7]AngewandteChemie-InternationalEdition,2016,vol.55,p.13326-13329    Angew.Chem.,2016,vol.128,p.13520-13523,4

[8]JournaloftheAmericanChemicalSociety,1964,vol.86,p.3566-3567

[9]Synthesis,1981,p.996-997

[10]TetrahedronLetters,1980,vol.21,p.4061-4064

[11]ChemicalCommunications,2016,vol.52,p.12195-12198

Literature
Quotation Request
Company Name:
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Additional Info:
SDS
Tags:15184-96-0 Molecular Formula|15184-96-0 MDL|15184-96-0 SMILES|15184-96-0 N,N-Dimethyl-4-nitrobenzylamine
Catalog No.: AA003SHL
15184-96-0,MFCD00035956
15184-96-0 | N,N-Dimethyl-4-nitrobenzylamine
Pack Size: 1g
Purity: 98%
in stock
$27.00 $19.00
Pack Size: 5g
Purity: ≥95%
in stock
$44.00 $31.00
Pack Size: 10g
Purity: 95%
in stock
$56.00 $39.00
Pack Size: 25g
Purity: 95%
in stock
$136.00 $95.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003SHL
Chemical Name: N,N-Dimethyl-4-nitrobenzylamine
CAS Number: 15184-96-0
Molecular Formula: C9H12N2O2
Molecular Weight: 180.2038
MDL Number: MFCD00035956
SMILES: CN(Cc1ccc(cc1)[N+](=O)[O-])C
Properties
BP: 262.4°C at 760 mmHg  
Form: Liquid  
Storage: Keep in dry area;2-8℃;  
Complexity: 169  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2  
Upstream Synthesis Route
124-40-3    100-11-8    15184-96-0 

[1]MedicinalChemistry,2016,vol.12,#5,p.489-498

[2]EuropeanJournalofMedicinalChemistry,2014,vol.86,p.257-269

[3]ArchivderPharmazie,2014,vol.347,#12,p.936-949

[4]Patent:WO2006/123145,2006,A1,.Locationinpatent:Page/Pagecolumn58

[5]JournaloftheAmericanChemicalSociety,1983,vol.105,#13,p.4136-4142

[6]Patent:KR2018/74094,2018,A,.Locationinpatent:Paragraph0098-0101

[7]BioorganicandMedicinalChemistryLetters,2004,vol.14,#9,p.2061-2065

7291-01-2    15184-96-0 

[1]JournaloftheAmericanChemicalSociety,2009,vol.131,#41,p.15032-15040

[2]Chemistry-AEuropeanJournal,2017,vol.23,#9,p.2005-2009

[3]RSCAdvances,2017,vol.7,#80,p.50729-50738

[4]JournaloftheAmericanChemicalSociety,2010,vol.132,#6,p.1770-1771

[5]AngewandteChemie-InternationalEdition,2013,vol.52,#44,p.11577-11580

[6]Angew.Chem.,2013,vol.125,#44,p.11791-11794,4

[7]Chemistry-AEuropeanJournal,2011,vol.17,#43,p.12186-12192

[8]AngewandteChemie-InternationalEdition,2016,vol.55,#42,p.13326-13329

[9]Angew.Chem.,2016,vol.128,#42,p.13520-13523,4

[10]JournaloftheAmericanChemicalSociety,1964,vol.86,p.3566-3567

[11]Synthesis,1981,#12,p.996-997

[12]TetrahedronLetters,1980,vol.21,#42,p.4061-4064

[13]ChemicalCommunications,2016,vol.52,#82,p.12195-12198

555-16-8    124-40-3    15184-96-0 

[1]SyntheticCommunications,2000,vol.30,#11,p.2001-2008

[2]Patent:WO2008/77885,2008,A2,.Locationinpatent:Page/Pagecolumn19

100-14-1    124-40-3    15184-96-0 

[1]JournalofMedicinalChemistry,2009,vol.52,#14,p.4466-4480

[2]ChemischeBerichte,1895,vol.28,p.1141

[3]ArchivderPharmazie,1962,vol.295/67,p.690-697

[4]BulletindelaSocieteChimiquedeFrance,1975,p.679-685

[5]JournaloftheChemicalSociety,1929,p.267

[6]JournaloftheChemicalSociety,1927,p.1904

[7]BioorganicandMedicinalChemistryLetters,2008,vol.18,#12,p.3641-3645

506-59-2    100-11-8    15184-96-0 

[1]JournalofMedicinalChemistry,2013,vol.56,#7,p.2975-2990

[2]Patent:EP2824108,2015,A1,.Locationinpatent:Paragraph0104

[3]Patent:US2015/166595,2015,A1,.Locationinpatent:Paragraph0222

Downstream Synthesis Route
64-18-6   
(4-nitro-benzyl)-hexamethylenetetraminium;chloride 
  15184-96-0 

[1]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1922,vol.174,p.689

3-chloro-propionicaciddodecylamide 
  15184-96-0   
(2-dodecylcarbamoyl-ethyl)-dimethyl-(4-nitro-benzyl)-ammonium;chloride 

[1]Patent:US2317999,1940,

15184-96-0    6406-74-2 

[1]RSCAdvances,2015,vol.5,p.47125-47130

[2]JournalofMedicinalChemistry,2013,vol.56,p.2975-2990

[3]Patent:WO2006/123145,2006,A1.Locationinpatent:Page/Pagecolumn58

[4]EuropeanJournalofMedicinalChemistry,2014,vol.86,p.257-269

[5]ArchivderPharmazie,2014,vol.347,p.936-949

[6]MedicinalChemistry,2016,vol.12,p.489-498

[7]Patent:CN109265453,2019,A.Locationinpatent:Paragraph0081;0087-0089

[8]Patent:KR2018/74094,2018,A.Locationinpatent:Paragraph0104-0109

[9]CollectionofCzechoslovakChemicalCommunications,1990,vol.55,p.282-295

[10]JournaloftheChemicalSociety,1935,p.871

[11]JournaloftheChemicalSociety,1927,p.1904

[12]Patent:US6166006,2000,A

[13]Patent:WO2008/77885,2008,A2.Locationinpatent:Page/Pagecolumn19

[14]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.3641-3645

[15]JournalofMedicinalChemistry,2009,vol.52,p.4466-4480

[16]Patent:US2006/58341,2006,A1.Locationinpatent:Page/Pagecolumn30

[17]Patent:EP2824108,2015,A1.Locationinpatent:Paragraph0105

[18]Patent:US2015/166595,2015,A1.Locationinpatent:Paragraph0223

[19]MedChemComm,2019,vol.10,p.465-477

[20]ChemicalandPharmaceuticalBulletin,2019,vol.67,p.351-360

64-18-6    100-97-0    100-14-1    15184-96-0 

[1]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1922,vol.174,p.689

7291-01-2    15184-96-0 

[1]JournaloftheAmericanChemicalSociety,2009,vol.131,p.15032-15040

[2]Chemistry-AEuropeanJournal,2017,vol.23,p.2005-2009

[3]RSCAdvances,2017,vol.7,p.50729-50738

[4]JournaloftheAmericanChemicalSociety,2010,vol.132,p.1770-1771

[5]AngewandteChemie-InternationalEdition,2013,vol.52,p.11577-11580    Angew.Chem.,2013,vol.125,p.11791-11794,4

[6]Chemistry-AEuropeanJournal,2011,vol.17,p.12186-12192

[7]AngewandteChemie-InternationalEdition,2016,vol.55,p.13326-13329    Angew.Chem.,2016,vol.128,p.13520-13523,4

[8]JournaloftheAmericanChemicalSociety,1964,vol.86,p.3566-3567

[9]Synthesis,1981,p.996-997

[10]TetrahedronLetters,1980,vol.21,p.4061-4064

[11]ChemicalCommunications,2016,vol.52,p.12195-12198

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