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627-64-5,MFCD00025527
Catalog No.:AA003QMA

627-64-5 | Fumaramide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$35.00   $25.00
- +
5g
96%
in stock  
$79.00   $55.00
- +
10g
>96.0%(N)
in stock  
$85.00   $60.00
- +
25g
>96.0%(N)
in stock  
$127.00   $89.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003QMA
Chemical Name:
Fumaramide
CAS Number:
627-64-5
Molecular Formula:
C4H6N2O2
Molecular Weight:
114.1026
MDL Number:
MFCD00025527
SMILES:
NC(=O)/C=C/C(=O)N
NSC Number:
16608
Properties
Properties
 
BP:
213.59°C (rough estimate)  
Form:
Solid  
MP:
290 °C (dec.)(lit.)  
Refractive Index:
1.4487 (estimate)  
Storage:
Room Temperature;Light sensitive;Keep in dry area;  

Computed Properties
 
Complexity:
123  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
1  
Formal Charge:
0  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-1.7  

Downstream Synthesis Route

[1]SiebertbeiZiegler;Schenck;Krockow[JustusLiebigsAnnalenderChemie,1942,vol.551,p.49]

[2]Mowry;Butler[OrganicSyntheses,1950,vol.30,p.46]deWolf;vandeStraete[BulletindelaClassedesSciences,AcademieRoyaledeBelgique,1935,vol.<5>21,p.218][ChemischesZentralblatt,1935,vol.106,#II,p.2658]deWolf;vandeStraete[BulletindesSocietesChimiquesBelges,1935,vol.44,p.294][BulletindelaClassedesSciences,AcademieRoyaledeBelgique,1935,vol.<5>21,p.224]Blomquist;Winslow[JournalofOrganicChemistry,1945,vol.10,p.149,157]

[3]CurrentPatentAssignee:GOODYEARTIRE&RUBBERCO-US2438019,1946,A

[4]CurrentPatentAssignee:GOODYEARTIRE&RUBBERCO-US2438019,1946,A

[5]Keiser;Kessler[AmericanChemicalJournal,1911,vol.46,p.526]

[6]McMaster;Langreck[JournaloftheAmericanChemicalSociety,1918,vol.40,p.970]

[7]CurrentPatentAssignee:DUPONTDENEMOURSINC-US2121551,1936,A

Literature

Title: A generic basis for some simple light-operated mechanical molecular machines.

Journal: Journal of the American Chemical Society 20041006

Title: DNA-templated organic synthesis and selection of a library of macrocycles.

Journal: Science (New York, N.Y.) 20040910

Title: A ribozyme with michaelase activity: synthesis of the substrate precursors.

Journal: Bioorganic & medicinal chemistry 20030117

Title: Plausible molecular mechanism for activation by fumarate and electron transfer of the dopamine beta-mono-oxygenase reaction.

Journal: The Biochemical journal 20021001

Title: Solution and solid-state models of peptide CH...O hydrogen bonds.

Journal: Journal of the American Chemical Society 20020925

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SDS
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Tags:627-64-5 Molecular Formula|627-64-5 MDL|627-64-5 SMILES|627-64-5 Fumaramide
Catalog No.: AA003QMA
627-64-5,MFCD00025527
627-64-5 | Fumaramide
Pack Size： 1g
Purity： 97%
in stock
$35.00 $25.00
Pack Size： 5g
Purity： 96%
in stock
$79.00 $55.00
Pack Size： 10g
Purity： >96.0%(N)
in stock
$85.00 $60.00
Pack Size： 25g
Purity： >96.0%(N)
in stock
$127.00 $89.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA003QMA
Chemical Name: Fumaramide
CAS Number: 627-64-5
Molecular Formula: C4H6N2O2
Molecular Weight: 114.1026
MDL Number: MFCD00025527
SMILES: NC(=O)/C=C/C(=O)N
NSC Number: 16608
Properties
BP: 213.59°C (rough estimate)  
Form: Solid  
MP: 290 °C (dec.)(lit.)  
Refractive Index: 1.4487 (estimate)  
Storage: Room Temperature;Light sensitive;Keep in dry area;  
Complexity: 123  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 1  
Formal Charge: 0  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -1.7  
Downstream Synthesis Route
627-64-5    764-42-1 

[1]SiebertbeiZiegler;Schenck;Krockow[JustusLiebigsAnnalenderChemie,1942,vol.551,p.49]

[2]Mowry;Butler[OrganicSyntheses,1950,vol.30,p.46]deWolf;vandeStraete[BulletindelaClassedesSciences,AcademieRoyaledeBelgique,1935,vol.<5>21,p.218][ChemischesZentralblatt,1935,vol.106,#II,p.2658]deWolf;vandeStraete[BulletindesSocietesChimiquesBelges,1935,vol.44,p.294][BulletindelaClassedesSciences,AcademieRoyaledeBelgique,1935,vol.<5>21,p.224]Blomquist;Winslow[JournalofOrganicChemistry,1945,vol.10,p.149,157]

[3]CurrentPatentAssignee:GOODYEARTIRE&RUBBERCO-US2438019,1946,A

[4]CurrentPatentAssignee:GOODYEARTIRE&RUBBERCO-US2438019,1946,A

[5]Keiser;Kessler[AmericanChemicalJournal,1911,vol.46,p.526]

[6]McMaster;Langreck[JournaloftheAmericanChemicalSociety,1918,vol.40,p.970]

[7]CurrentPatentAssignee:DUPONTDENEMOURSINC-US2121551,1936,A

Literature fold

Title: A generic basis for some simple light-operated mechanical molecular machines.

Journal: Journal of the American Chemical Society20041006

Title: DNA-templated organic synthesis and selection of a library of macrocycles.

Journal: Science (New York, N.Y.)20040910

Title: A ribozyme with michaelase activity: synthesis of the substrate precursors.

Journal: Bioorganic & medicinal chemistry20030117

Title: Plausible molecular mechanism for activation by fumarate and electron transfer of the dopamine beta-mono-oxygenase reaction.

Journal: The Biochemical journal20021001

Title: Solution and solid-state models of peptide CH...O hydrogen bonds.

Journal: Journal of the American Chemical Society20020925

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