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86-79-3,MFCD00004962
Catalog No.:AA003HCM
86-79-3 | 2-Hydroxycarbazole, 97%
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1g
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5g
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  • Technical Information
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  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003HCM
Chemical Name:
2-Hydroxycarbazole, 97%
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
Computed 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  

Synonyms
 
2-hydroxycarbazole 
2-Hydroxycarbazole 
BRN 0135859 
GWPGDZPXOZATKL-UHFFFAOYSA-N 
7-hydroxycarbazole 
2-hydroxy carbazole 
PubChem9945 
PubChem9949 
2-hydroxy-9H-carbazol 
2-Hydroxy-9H-carbazole 
AC1L3QFH 
AC1Q78YU 
9H-Carbazol-2-ol 
Oprea1_146166 
5-21-04-00005 (Beilstein Handbook Reference) 
SCHEMBL150279 
CHEMBL1170901 
CTK3J2805 
GWPGDZPXOZATKL-UHFFFAOYSA- 
DTXSID50235340 
HMS1719L15 
ZINC2132858 
SBB056583 
86-79-3 
STL554147 
AKOS001079611 
MCULE-8116402305 
RTR-038063 
AS-15921 
BC221375 
CJ-32846 
LS-51852 
R349 
DB-021202 
Carbazol-2-ol 
TR-038063 
CS-0046240 
FT-0082176 
FT-0602043 
ST50308430 
A841830 
I14-51461 
InChI=1/C12H9NO/c14-8-5-6-10-9-3-1-2-4-11(9)13-12(10)7-8/h1-7,13-14H 
2-Hydroxycarbazol 
C12H9NO 
2-Carbazolol 
C12-H9-N-O 
CID93551 
CCRIS 5301 
EINECS 201-699-7 
MFCD00004962 
2-Hydroxycarbazole, 97% 
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: Kinesin spindle protein (KSP) inhibitors with 2,3-fused indole scaffolds.

Journal: Journal of medicinal chemistry 20100708

Title: Inhibitory effect of hydroxyindoles and their analogues on human melanoma tyrosinase.

Journal: Zeitschrift fur Naturforschung. C, Journal of biosciences 20100101

Title: Substrate specificity and structural characteristics of the novel Rieske nonheme iron aromatic ring-hydroxylating oxygenases NidAB and NidA3B3 from Mycobacterium vanbaalenii PYR-1.

Journal: mBio 20100101

Title: First synthesis of dimethyl-1H-isochromeno[3,4-b]carbazoles.

Journal: Natural product communications 20090701

Title: Synthesis and activity of carbazole derivatives against Mycobacterium tuberculosis.

Journal: ChemMedChem 20060801

Title: Hydroxylation of carbazoles by Aspergillus flavus VKM F-1024.

Journal: FEMS microbiology letters 20040601

Title: Photochemistry of 2-acyloxycarbazoles. A potential tool in the synthesis of carbazole alkaloids.

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20040401

Title: Distinct pharmacology of 2-hydroxycarbazole-induced Ca2+ release in the sea urchin egg.

Journal: The Journal of pharmacology and experimental therapeutics 20010801

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