Home Indole and Oxindoles 272-49-1
272-49-1,MFCD00971977
Catalog No.:AA0033U5

272-49-1 | 4-Azaindole

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1g
98%
in stock  
$13.00   $9.00
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5g
95%
in stock  
$30.00   $21.00
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10g
95%
in stock  
$54.00   $38.00
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  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0033U5
Chemical Name:
4-Azaindole
CAS Number:
272-49-1
Molecular Formula:
C7H6N2
Molecular Weight:
118.1359
MDL Number:
MFCD00971977
SMILES:
c1cnc2c(c1)[nH]cc2
Properties
Properties
 
BP:
273.8°C at 760 mmHg  
Form:
Solid  
MP:
126-127 °C  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
103  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
XLogP3:
1.1  

Literature

Title: Inhibitors of HIV-1 attachment. Part 10. The discovery and structure-activity relationships of 4-azaindole cores.

Journal: Bioorganic & medicinal chemistry letters 20130101

Title: Spectroscopic study of the ground and excited state prototropic equilibria of 4-azaindole.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20121101

Title: Blue fluorescent amino acids as in vivo building blocks for proteins.

Journal: Chembiochem : a European journal of chemical biology 20100215

Title: Synthesis and antiproliferative activity of pyrrolo[3,2-b]pyridine derivatives against melanoma.

Journal: Bioorganic & medicinal chemistry letters 20100101

Title: Synthesis of 4- and 6-azaindoles via the Fischer reaction.

Journal: Organic letters 20091119

Title: Discovery of 4-azaindoles as novel inhibitors of c-Met kinase.

Journal: Bioorganic & medicinal chemistry letters 20090515

Title: Synthesis of C3-substituted 4-azaindoles: an easy access to 4-azamelatonin and protected 4-azatryptophan.

Journal: The Journal of organic chemistry 20080919

Title: Excited state tautomerization of azaindole.

Journal: Organic & biomolecular chemistry 20051021

Title: Preparation of 4-azaindole and 7-azaindole dimers with a bisalkoxyalkyl spacer in order to preferentially target melatonin MT1 receptors over melatonin MT2 receptors.

Journal: European journal of medicinal chemistry 20040601

Title: Unexpected ring transformation to pyrrolo[3.2-b]pyridine derivatives. Fused azolium salts. 22.

Journal: The Journal of organic chemistry 20030711

Title: Novel potent 5-HT(1F) receptor agonists: structure-activity studies of a series of substituted N-[3-(1-methyl-4-piperidinyl)-1H-pyrrolo[3,2-b]pyridin-5-yl]amides.

Journal: Journal of medicinal chemistry 20030703

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