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625-50-3,MFCD00009029
Catalog No.:AA003SX9

625-50-3 | N-Ethylacetamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$12.00   $8.00
- +
25g
98%
in stock  
$24.00   $17.00
- +
100g
98%
in stock  
$93.00   $65.00
- +
500g
97%
in stock  
$452.00   $317.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003SX9
Chemical Name:
N-Ethylacetamide
CAS Number:
625-50-3
Molecular Formula:
C4H9NO
Molecular Weight:
87.1204
MDL Number:
MFCD00009029
SMILES:
CCNC(=O)C
NSC Number:
406307
Properties
Properties
 
BP:
205.0°C  
Form:
Liquid  
MP:
-32°C  
Refractive Index:
n20/D 1.433(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
51.5  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
1  
XLogP3:
-0.1  

Downstream Synthesis Route

[1]Sukata,Kazuaki[BulletinoftheChemicalSocietyofJapan,1985,vol.58,#3,p.838-843]

[2]Nicholas;Erickson[JournaloftheAmericanChemicalSociety,1926,vol.48,p.2175]Erickson[ChemischeBerichte,1926,vol.59,p.2668]

[3]White;Morrison;Anderson[JournaloftheAmericanChemicalSociety,1924,vol.46,p.967]

[4]White;Morrison;Anderson[JournaloftheAmericanChemicalSociety,1924,vol.46,p.967]Nicholas;Erickson[JournaloftheAmericanChemicalSociety,1926,vol.48,p.2175]

[1]Hantzsch[ChemischeBerichte,1891,vol.24,p.4021]

[2]Locationinpatent:experimentalpartGanguly,NemaiC.;Mondal,Pallab[Synthesis,2010,#21,p.3705-3709]

[1]Franchimont;Dubsky[RecueildesTravauxChimiquesdesPays-Bas,1911,vol.30,p.192][ChemischesZentralblatt,1911,vol.82,#I,p.207]Parketal.[JournaloftheAmericanChemicalSociety,1952,vol.74,p.1010]

[2]Naumov,Yu.A.etal.[JournalofappliedchemistryoftheUSSR,1974,vol.47,p.1945-1947][ZhurnalPrikladnoiKhimii(Sankt-Peterburg,RussianFederation),1974,vol.47,p.1888-1890]

[1]CurrentPatentAssignee:I.G.Farbenind.-FR761932,1934,A[Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.21,p.187][Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.21,p.187]

[2]CurrentPatentAssignee:I.G.FARBENINDUSTRIEAG(historic)-US2166971,1933,A

[3]CurrentPatentAssignee:I.G.FARBENINDUSTRIEAG(historic)-DE599103,1934,C[Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.21,p.189][Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.21,p.189]

[1]CurrentPatentAssignee:FUJIANMEDICALUNIVERSITY-CN110218158,2019,ALocationinpatent:Paragraph0093

[2]Kuroki;Kanesaka;Yamada;Imoto[ChemicalandPharmaceuticalBulletin,1987,vol.35,#10,p.4203-4207]

[3]Jur'ewetal.[ZhurnalObshcheiKhimii,1959,vol.29,p.2594,2595,2596;engl.Ausg.S.2557,2558]

[4]CurrentPatentAssignee:CLARIANTAG-US2011/92722,2011,A1Locationinpatent:Page/Pagecolumn9

Literature

Title: Pentacyclic polyketides from Endiandra kingiana as inhibitors of the Bcl-xL/Bak interaction.

Journal: Phytochemistry 20110801

Title: Fractional Stokes-Einstein-Debye relation and orientational entropy effects in strongly hydrogen-bonded liquid amides.

Journal: Physical chemistry chemical physics : PCCP 20110307

Title: Involvement of basal protein kinase C and extracellular signal-regulated kinase 1/2 activities in constitutive internalization of AMPA receptors in cerebellar Purkinje cells.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience 20060503

Title: Synthesis, antioxidant activity and structure-activity relationships for a new series of 2-(N-acylaminoethyl)indoles with melatonin-like cytoprotective activity.

Journal: Journal of pineal research 20060401

Title: Identification of dielectric and structural relaxations in glass-forming secondary amides.

Journal: The Journal of chemical physics 20050801

Title: Substituent effects on the in situ activation of the double activated cross-linking reaction.

Journal: Nucleic acids symposium series (2004) 20050101

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