Home Other Building Blocks 2-Hydroxycarbazole

2-Hydroxycarbazole

CAS No.:
86-79-3
Catalog Number:
AG003HFE
Molecular Formula:
C12H9NO
Molecular Weight:
183.2060
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$60
- +
5g
95%
In Stock USA
United States
$121
- +
Product Description
Catalog Number:
AG003HFE
Chemical Name:
2-Hydroxycarbazole
CAS Number:
86-79-3
Molecular Formula:
C12H9NO
Molecular Weight:
183.2060
MDL Number:
MFCD00004962
IUPAC Name:
9H-carbazol-2-ol
InChI:
InChI=1S/C12H9NO/c14-8-5-6-10-9-3-1-2-4-11(9)13-12(10)7-8/h1-7,13-14H
InChI Key:
GWPGDZPXOZATKL-UHFFFAOYSA-N
SMILES:
Oc1ccc2c(c1)[nH]c1c2cccc1
EC Number:
201-699-7
Properties
Complexity:
218  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
183.068g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
183.21g/mol
Monoisotopic Mass:
183.068g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
36A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.5  
Literature
Title Journal
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Kinesin spindle protein (KSP) inhibitors with 2,3-fused indole scaffolds. Journal of medicinal chemistry 20100708
Inhibitory effect of hydroxyindoles and their analogues on human melanoma tyrosinase. Zeitschrift fur Naturforschung. C, Journal of biosciences 20100101
Substrate specificity and structural characteristics of the novel Rieske nonheme iron aromatic ring-hydroxylating oxygenases NidAB and NidA3B3 from Mycobacterium vanbaalenii PYR-1. mBio 20100101
First synthesis of dimethyl-1H-isochromeno[3,4-b]carbazoles. Natural product communications 20090701
Synthesis and activity of carbazole derivatives against Mycobacterium tuberculosis. ChemMedChem 20060801
Hydroxylation of carbazoles by Aspergillus flavus VKM F-1024. FEMS microbiology letters 20040601
Photochemistry of 2-acyloxycarbazoles. A potential tool in the synthesis of carbazole alkaloids. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20040401
Distinct pharmacology of 2-hydroxycarbazole-induced Ca2+ release in the sea urchin egg. The Journal of pharmacology and experimental therapeutics 20010801
Properties