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19311-91-2,MFCD00010816
Catalog No.:AA00358F

19311-91-2 | N,N-Diethylsalicylamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$10.00   $7.00
- +
5g
95%
in stock  
$19.00   $13.00
- +
25g
95%
in stock  
$68.00   $47.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00358F
Chemical Name:
N,N-Diethylsalicylamide
CAS Number:
19311-91-2
Molecular Formula:
C11H15NO2
Molecular Weight:
193.2423
MDL Number:
MFCD00010816
SMILES:
CCN(C(=O)c1ccccc1O)CC
Properties
Properties
 
BP:
382.6°C at 760 mmHg  
Form:
Solid  
MP:
93-97 °C(lit.)  
Refractive Index:
1.5080 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
190  
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:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.2  

Upstream Synthesis Route

[1]OrganicLetters,2012,vol.14,#16,p.4210-4213

[2]JournaloftheAmericanChemicalSociety,2016,vol.138,#29,p.9166-9171

[3]JournalofOrganicChemistry,1982,vol.47,#1,p.34-46

[4]JournalofOrganicChemistry,1987,vol.52,#4,p.674-676

[5]Tetrahedron,1992,vol.48,#23,p.4863-4878

[1]AnnalesdeChimie(Cachan,France),1938,vol.<11>10,p.559,597

[2]JournalofOrganicChemistryUSSR(EnglishTranslation),1982,vol.18,#6,p.1115-1119

[3]ZhurnalOrganicheskoiKhimii,1982,vol.18,#6,p.1287-1291

[4]Patent:WO2005/61484,2005,A1,.Locationinpatent:Page/Pagecolumn45-46

[5]JournalofSurfactantsandDetergents,2013,vol.16,#4,p.581-585

[1]OrganicLetters,2010,vol.12,#9,p.2024-2027

[1]Tetrahedron,1996,vol.52,#43,p.13623-13640

[2]TetrahedronLetters,1983,vol.24,#42,p.4515-4518

[3]HelveticaChimicaActa,1989,vol.72,#8,p.1649-1657

[1]AngewandteChemie-InternationalEdition,2014,vol.53,#34,p.9026-9029

[2]Angew.Chem.,2014,vol.126,#34,p.9172-9175,4

[3]JournalofOrganicChemistry,1983,vol.48,#11,p.1935-1937

[4]EuropeanJournalofOrganicChemistry,2018,vol.2018,#4,p.440-446

[5]Synlett,2009,#17,p.2777-2782

[6]JournalofOrganicChemistryUSSR(EnglishTranslation),1982,vol.18,#6,p.1115-1119

[7]ZhurnalOrganicheskoiKhimii,1982,vol.18,#6,p.1287-1291

Downstream Synthesis Route

[1]AnnalesdeChimie(Cachan,France),1938,vol.<11>10,p.559,597

[1]AnnalidiChimica,1955,vol.45,p.205,213

[2]JournalofPharmaceuticalSciences,1990,vol.79,p.651-651

[1]JournalofPharmacyandPharmacology,1958,vol.10,p.96,100

[1]JournaloftheChemicalSociety.PerkintransactionsII,1989,p.199-208

[2]JournaloftheAmericanChemicalSociety,1947,vol.69,p.2913

[1]JournalofPharmacyandPharmacology,1958,vol.10,p.96,100

Literature

Title: Copper-catalyzed guanidinylation of aryl iodides: the formation of N,N'-disubstituted guanidines.

Journal: Organic letters 20100319

Title: Copper-catalyzed amination of (bromophenyl)ethanolamine for a concise synthesis of aniline-containing analogues of NMDA NR2B antagonist ifenprodil.

Journal: Organic & biomolecular chemistry 20100307

Title: Mild and efficient copper-catalyzed amination of aryl bromides with primary alkylamines.

Journal: Organic letters 20030320

Quotation Request
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SDS
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Tags:19311-91-2 Molecular Formula|19311-91-2 MDL|19311-91-2 SMILES|19311-91-2 N,N-Diethylsalicylamide
Catalog No.: AA00358F
19311-91-2,MFCD00010816
19311-91-2 | N,N-Diethylsalicylamide
Pack Size： 1g
Purity： 95%
in stock
$10.00 $7.00
Pack Size： 5g
Purity： 95%
in stock
$19.00 $13.00
Pack Size： 25g
Purity： 95%
in stock
$68.00 $47.00
Quantity
- +
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Technical Information
Catalog Number: AA00358F
Chemical Name: N,N-Diethylsalicylamide
CAS Number: 19311-91-2
Molecular Formula: C11H15NO2
Molecular Weight: 193.2423
MDL Number: MFCD00010816
SMILES: CCN(C(=O)c1ccccc1O)CC
Properties
BP: 382.6°C at 760 mmHg  
Form: Solid  
MP: 93-97 °C(lit.)  
Refractive Index: 1.5080 (estimate)  
Storage: Keep in dry area;Room Temperature;  
Complexity: 190  
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: 2  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.2  
Upstream Synthesis Route
1696-17-9    19311-91-2 

[1]OrganicLetters,2012,vol.14,#16,p.4210-4213

[2]JournaloftheAmericanChemicalSociety,2016,vol.138,#29,p.9166-9171

[3]JournalofOrganicChemistry,1982,vol.47,#1,p.34-46

[4]JournalofOrganicChemistry,1987,vol.52,#4,p.674-676

[5]Tetrahedron,1992,vol.48,#23,p.4863-4878

109-89-7    1441-87-8    19311-91-2 

[1]AnnalesdeChimie(Cachan,France),1938,vol.<11>10,p.559,597

[2]JournalofOrganicChemistryUSSR(EnglishTranslation),1982,vol.18,#6,p.1115-1119

[3]ZhurnalOrganicheskoiKhimii,1982,vol.18,#6,p.1287-1291

[4]Patent:WO2005/61484,2005,A1,.Locationinpatent:Page/Pagecolumn45-46

[5]JournalofSurfactantsandDetergents,2013,vol.16,#4,p.581-585

444-30-4    109-89-7    19311-91-2 

[1]OrganicLetters,2010,vol.12,#9,p.2024-2027

51674-10-3    19311-91-2 

[1]Tetrahedron,1996,vol.52,#43,p.13623-13640

[2]TetrahedronLetters,1983,vol.24,#42,p.4515-4518

[3]HelveticaChimicaActa,1989,vol.72,#8,p.1649-1657

65009-00-9    19311-91-2 

[1]AngewandteChemie-InternationalEdition,2014,vol.53,#34,p.9026-9029

[2]Angew.Chem.,2014,vol.126,#34,p.9172-9175,4

[3]JournalofOrganicChemistry,1983,vol.48,#11,p.1935-1937

[4]EuropeanJournalofOrganicChemistry,2018,vol.2018,#4,p.440-446

[5]Synlett,2009,#17,p.2777-2782

[6]JournalofOrganicChemistryUSSR(EnglishTranslation),1982,vol.18,#6,p.1115-1119

[7]ZhurnalOrganicheskoiKhimii,1982,vol.18,#6,p.1287-1291

Downstream Synthesis Route
19311-91-2    925-90-6    610-99-1 

[1]AnnalesdeChimie(Cachan,France),1938,vol.<11>10,p.559,597

91731-53-2    19311-91-2 

[1]AnnalidiChimica,1955,vol.45,p.205,213

[2]JournalofPharmaceuticalSciences,1990,vol.79,p.651-651

19311-91-2    556-52-5    101777-18-8 

[1]JournalofPharmacyandPharmacology,1958,vol.10,p.96,100

118-55-8    109-89-7    19311-91-2 

[1]JournaloftheChemicalSociety.PerkintransactionsII,1989,p.199-208

[2]JournaloftheAmericanChemicalSociety,1947,vol.69,p.2913

19311-91-2    2210-79-9    102372-99-6 

[1]JournalofPharmacyandPharmacology,1958,vol.10,p.96,100

Literature fold

Title: Copper-catalyzed guanidinylation of aryl iodides: the formation of N,N'-disubstituted guanidines.

Journal: Organic letters20100319

Title: Copper-catalyzed amination of (bromophenyl)ethanolamine for a concise synthesis of aniline-containing analogues of NMDA NR2B antagonist ifenprodil.

Journal: Organic & biomolecular chemistry20100307

Title: Mild and efficient copper-catalyzed amination of aryl bromides with primary alkylamines.

Journal: Organic letters20030320

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