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132160-50-0

132160-50-0 | 9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy-

CAS No: 132160-50-0 Catalog No: AG0010BX MDL No:

Product Description

Catalog Number:
AG0010BX
Chemical Name:
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy-
CAS Number:
132160-50-0
Molecular Formula:
C15H13NO3
Molecular Weight:
255.2686
IUPAC Name:
2,7-dimethoxy-9H-carbazole-3-carbaldehyde
InChI:
InChI=1S/C15H13NO3/c1-18-10-3-4-11-12-5-9(8-17)15(19-2)7-14(12)16-13(11)6-10/h3-8,16H,1-2H3
InChI Key:
KSAHTWWUVLYPSK-UHFFFAOYSA-N
SMILES:
COc1ccc2c(c1)[nH]c1c2cc(c(c1)OC)C=O

Properties

Complexity:
335  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
255.09g/mol
Formal Charge:
0
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
255.273g/mol
Monoisotopic Mass:
255.09g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
51.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.8  

Literature

Title Journal
Bioactive carbazole alkaloids from Clausena wallichii roots. Journal of natural products 20120427
Induction of cell cycle arrest by the carbazole alkaloid Clauszoline-I from Clausena vestita D. D. Tao via inhibition of the PKCδ phosphorylation. European journal of medicinal chemistry 20120101
Glycozolidal. Acta crystallographica. Section E, Structure reports online 20110701
Claurailas A-D, cytotoxic carbazole alkaloids from the roots of Clausena harmandiana. Journal of natural products 20110225
Determination of a pyranocoumarin and three carbazole compounds in Clausena excavata by RP-HPLC. Journal of chromatographic science 20100701
Synthesis and activity of carbazole derivatives against Mycobacterium tuberculosis. ChemMedChem 20060801
Anti-HIV-1 constituents from Clausena excavata: Part II. Carbazoles and a pyranocoumarin. Phytotherapy research : PTR 20050801

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