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4394-85-8,MFCD00006170
Catalog No.:AA0035B1

4394-85-8 | N-Formylmorpholine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25g
≥98%
in stock  
$8.00   $6.00
- +
100g
98%
in stock  
$17.00   $12.00
- +
500g
98%
in stock  
$22.00   $16.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0035B1
Chemical Name:
N-Formylmorpholine
CAS Number:
4394-85-8
Molecular Formula:
C5H9NO2
Molecular Weight:
115.1305
MDL Number:
MFCD00006170
SMILES:
O=CN1CCOCC1
NSC Number:
14833
Properties
Properties
 
BP:
236.5°C at 760 mmHg  
Form:
Liquid  
MP:
23 °C(lit.);  
Refractive Index:
n20/D 1.485(lit.)  
Solubility:
SOLUBLE  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
78.5  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.6  

Upstream Synthesis Route

[1]Synthesis,1987,#11,p.998-1001

[2]JournalofMaterialsChemistry,1998,vol.8,#4,p.833-835

[1]Patent:US2009/170907,2009,A1,.Locationinpatent:Page/Pagecolumn59

[1]Patent:US5569655,1996,A,

[1]Tetrahedron,1998,vol.54,#47,p.14327-14340

[1]OrganicLetters,2018,vol.20,#18,p.5861-5865

Downstream Synthesis Route
693-93-6    4394-85-8   
4-methyl-5-oxazolecarboxaldehyde 

[1]GazzettaChimicaItaliana,1988,vol.118,p.211-232

[1]JournaloftheChemicalSociety.PerkintransactionsI,1990,p.329-331

[1]CollectionofCzechoslovakChemicalCommunications,1987,vol.52,p.1006-1014

[1]Patent:CN109232612,2019,A.Locationinpatent:Paragraph0215;0216;0217

[2]Synthesis,1987,p.998-1001

[1]Dondoni,Alessandro;Fantin,Giancarlo;Fogagnolo,Marco;Medici,Alessandro;Pedrini,Paola[Synthesis,1987,#11,p.998-1001]

Literature

Title: Use of Linear Free Energy Relationships (LFERs) to elucidate the mechanisms of reaction of a γ-methyl-β-alkynyl and an ortho-substituted aryl chloroformate ester.

Journal: International journal of molecular sciences 20120101

Title: Protease-activated drug development.

Journal: Theranostics 20120101

Title: A combined experimental and theoretical quantum chemical studies on 4-morpholinecarboxaldehyde.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20110901

Title: Microwave-assisted synthesis of quinoline, isoquinoline, quinoxaline and quinazoline derivatives as CB2 receptor agonists.

Journal: Bioorganic & medicinal chemistry 20110115

Title: Reduction of VOC emissions by a membrane-based gas absorption process.

Journal: Journal of environmental sciences (China) 20090101

Title: Ethyl (E)-3-(2-hydroxyphenyl)-2-(morpholinocarbonyl)propenoate.

Journal: Acta crystallographica. Section C, Crystal structure communications 20040701

Title: The use of solid-phase supported 1-N-piperazine-4-N-carboxaldehyde in Vilsmeier reactions.

Journal: Journal of combinatorial chemistry 20040101

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SDS
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Tags:4394-85-8 Molecular Formula|4394-85-8 MDL|4394-85-8 SMILES|4394-85-8 N-Formylmorpholine
Catalog No.: AA0035B1
4394-85-8,MFCD00006170
4394-85-8 | N-Formylmorpholine
Pack Size： 25g
Purity： ≥98%
in stock
$8.00 $6.00
Pack Size： 100g
Purity： 98%
in stock
$17.00 $12.00
Pack Size： 500g
Purity： 98%
in stock
$22.00 $16.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0035B1
Chemical Name: N-Formylmorpholine
CAS Number: 4394-85-8
Molecular Formula: C5H9NO2
Molecular Weight: 115.1305
MDL Number: MFCD00006170
SMILES: O=CN1CCOCC1
NSC Number: 14833
Properties
BP: 236.5°C at 760 mmHg  
Form: Liquid  
MP: 23 °C(lit.);  
Refractive Index: n20/D 1.485(lit.)  
Solubility: SOLUBLE  
Stability: Hygroscopic  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 78.5  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.6  
Upstream Synthesis Route
3034-53-5    4394-85-8    10200-59-6 

[1]Synthesis,1987,#11,p.998-1001

[2]JournalofMaterialsChemistry,1998,vol.8,#4,p.833-835

4394-85-8    116045-56-8    1003-32-3 

[1]Patent:US2009/170907,2009,A1,.Locationinpatent:Page/Pagecolumn59

3581-89-3    4394-85-8    13838-78-3 

[1]Patent:US5569655,1996,A,

4394-85-8    136613-57-5    63136-60-7 

[1]Tetrahedron,1998,vol.54,#47,p.14327-14340

110-91-8    4394-85-8    38952-62-4 

[1]OrganicLetters,2018,vol.20,#18,p.5861-5865

Downstream Synthesis Route
693-93-6    4394-85-8   
4-methyl-5-oxazolecarboxaldehyde 

[1]GazzettaChimicaItaliana,1988,vol.118,p.211-232

3034-52-4    4394-85-8    1011-41-2 

[1]JournaloftheChemicalSociety.PerkintransactionsI,1990,p.329-331

4394-85-8    20358-03-6    112446-68-1 

[1]CollectionofCzechoslovakChemicalCommunications,1987,vol.52,p.1006-1014

4394-85-8    79265-30-8    116045-56-8 

[1]Patent:CN109232612,2019,A.Locationinpatent:Paragraph0215;0216;0217

[2]Synthesis,1987,p.998-1001

4394-85-8    108306-53-2    116045-55-7 

[1]Dondoni,Alessandro;Fantin,Giancarlo;Fogagnolo,Marco;Medici,Alessandro;Pedrini,Paola[Synthesis,1987,#11,p.998-1001]

Literature fold

Title: Use of Linear Free Energy Relationships (LFERs) to elucidate the mechanisms of reaction of a γ-methyl-β-alkynyl and an ortho-substituted aryl chloroformate ester.

Journal: International journal of molecular sciences20120101

Title: Protease-activated drug development.

Journal: Theranostics20120101

Title: A combined experimental and theoretical quantum chemical studies on 4-morpholinecarboxaldehyde.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy20110901

Title: Microwave-assisted synthesis of quinoline, isoquinoline, quinoxaline and quinazoline derivatives as CB2 receptor agonists.

Journal: Bioorganic & medicinal chemistry20110115

Title: Reduction of VOC emissions by a membrane-based gas absorption process.

Journal: Journal of environmental sciences (China)20090101

Title: Ethyl (E)-3-(2-hydroxyphenyl)-2-(morpholinocarbonyl)propenoate.

Journal: Acta crystallographica. Section C, Crystal structure communications20040701

Title: The use of solid-phase supported 1-N-piperazine-4-N-carboxaldehyde in Vilsmeier reactions.

Journal: Journal of combinatorial chemistry20040101

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