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Home Imidazoles 19141-85-6
19141-85-6,MFCD20617036
Catalog No.:AA001IIB

19141-85-6 | 4-Ethyl-1H-imidazole

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
96%
in stock  
$70.00   $49.00
- +
1g
96%
in stock  
$163.00   $114.00
- +
5g
96%
in stock  
$549.00   $384.00
- +
10g
96%
in stock  
$1,084.00   $759.00
- +
25g
96%
in stock  
$2,692.00   $1,884.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA001IIB
Chemical Name:
4-Ethyl-1H-imidazole
CAS Number:
19141-85-6
Molecular Formula:
C5H8N2
Molecular Weight:
96.1304
MDL Number:
MFCD20617036
SMILES:
CCc1cnc[nH]1
Properties
Computed Properties
 
Complexity:
54  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
0.8  

Downstream Synthesis Route
19141-85-6    98-88-4   
furan-2,3,5(4H)-trionepyridine(1:1) 
  132962-63-1 

[1]Windaus;Langenbeck[ChemischeBerichte,1922,vol.55,p.3708]

[1]Windaus;Langenbeck[ChemischeBerichte,1922,vol.55,p.3708]

4-ethyl-4-tosyl-2-oxazoline 
  19141-85-6 

[1]Horne,DavidA.;Yakushijin,Kenichi;Buechi,George[Heterocycles,1994,vol.39,#1,p.139-154]

5-ethyl-4-tosyl-2-oxazoline 
  19141-85-6 

[1]Horne,DavidA.;Yakushijin,Kenichi;Buechi,George[Heterocycles,1994,vol.39,#1,p.139-154]

Literature

Title: The catalytic aspartate is protonated in the Michaelis complex formed between trypsin and an in vitro evolved substrate-like inhibitor: a refined mechanism of serine protease action.

Journal: The Journal of biological chemistry 20110204

Title: Iron porphyrins with different imidazole ligands. A theoretical comparative study.

Journal: The journal of physical chemistry. A 20100909

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SDS
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