Home Indole and Oxindoles 5814-93-7
5814-93-7,MFCD00152109
Catalog No.:AA00EBCM

5814-93-7 | 3-(1H-Indol-3-yl)propanamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$66.00   $46.00
- +
1g
97%
in stock  
$140.00   $98.00
- +
5g
97%
in stock  
$610.00   $427.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00EBCM
Chemical Name:
3-(1H-Indol-3-yl)propanamide
CAS Number:
5814-93-7
Molecular Formula:
C11H12N2O
Molecular Weight:
188.2258
MDL Number:
MFCD00152109
SMILES:
NC(=O)CCc1c[nH]c2c1cccc2
NSC Number:
523262
Properties
Properties
 
BP:
487.6°C at 760 mmHg  
Form:
Solid  
MP:
169-170 °C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
217  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
1.1  

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: A novel endogenous indole protects rodent mitochondria and extends rotifer lifespan.

Journal: PloS one 20100101

Title: A novel indole-3-propanamide exerts its immunosuppressive activity by inhibiting JAK3 in T cells.

Journal: The Journal of pharmacology and experimental therapeutics 20091101

Title: A new Erythrinan alkaloid from the seed of Erythrina addisoniae.

Journal: Archives of pharmacal research 20090301

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Title: New N-pyridinyl(methyl)-N1-substituted-3-indolepropanamides acting as topical and systemic anti-inflammatory agents.

Journal: Journal of enzyme inhibition and medicinal chemistry 20030401

Title: Synthesis and analytical evaluation by voltammetric studies of some new indole-3-propionamide derivatives.

Journal: Farmaco (Societa chimica italiana : 1989) 20011101

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SDS
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