Home Other Building Blocks 1,2,3,4-Tetrahydrocarbazole

1,2,3,4-Tetrahydrocarbazole

CAS No.:
942-01-8
Catalog Number:
AG003DA7
Molecular Formula:
C12H13N
Molecular Weight:
171.2383
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$19
- +
5g
95%
In Stock USA
United States
$38
- +
25g
95%
In Stock USA
United States
$90
- +
100g
95%
In Stock USA
United States
$207
- +
Product Description
Catalog Number:
AG003DA7
Chemical Name:
1,2,3,4-Tetrahydrocarbazole
CAS Number:
942-01-8
Molecular Formula:
C12H13N
Molecular Weight:
171.2383
MDL Number:
MFCD00004959
IUPAC Name:
2,3,4,9-tetrahydro-1H-carbazole
InChI:
InChI=1S/C12H13N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1,3,5,7,13H,2,4,6,8H2
InChI Key:
XKLNOVWDVMWTOB-UHFFFAOYSA-N
SMILES:
C1CCc2c(C1)[nH]c1c2cccc1
EC Number:
213-385-7
UNII:
8ZLK0TSX93
NSC Number:
17329
Properties
Complexity:
190  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
171.105g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
171.243g/mol
Monoisotopic Mass:
171.105g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
15.8A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
3.3  
Literature
Title Journal
Enantioselective synthesis of spiro cyclopentane-1,3'-indoles and 2,3,4,9-tetrahydro-1H-carbazoles by iridium-catalyzed allylic dearomatization and stereospecific migration. Angewandte Chemie (International ed. in English) 20120213
Synthesis of 9-substituted 2,3,4,9-tetrahydro-1H-carbazole derivatives and evaluation of their anti-prion activity in TSE-infected cells. European journal of medicinal chemistry 20111101
An entry to the azocino[4,3-b]indole framework through a dehydrogenative activation of 1,2,3,4-tetrahydrocarbazoles mediated by DDQ: formal synthesis of (±)-uleine. The Journal of organic chemistry 20110107
Potent and highly selective DP1 antagonists with 2,3,4,9-tetrahydro-1H-carbazole as pharmacophore. Bioorganic & medicinal chemistry letters 20101215
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
One-pot synthesis of new substituted 1,2,3,4-tetrahydrocarbazoles via Petasis reaction. Journal of combinatorial chemistry 20100913
An enantioselective approach to highly substituted tetrahydrocarbazoles through hydrogen bonding-catalyzed cascade reactions. Organic letters 20100305
Derivatization of bioactive carbazoles by the biphenyl-degrading bacterium Ralstonia sp. strain SBUG 290. Applied microbiology and biotechnology 20090501
Synthesis and in-vitro antitumor activities of some mannich bases of 9-alkyl-1,2,3,4-tetrahydrocarbazole-1-ones. Archiv der Pharmazie 20090301
Indole and its alkyl-substituted derivatives protect erythrocyte and DNA against radical-induced oxidation. Journal of biochemical and molecular toxicology 20090101
2,3,4,9-Tetra-hydro-1H-carbazole. Acta crystallographica. Section E, Structure reports online 20081201
The energetics of tetrahydrocarbazole aromatization over Pd(111): a computational analysis. The Journal of chemical physics 20080314
Binding of methoxy-substituted N1-benzenesulfonylindole analogs at human 5-HT6 serotonin receptors. Bioorganic & medicinal chemistry letters 20060715
Design and synthesis of 2,3,4,9-tetrahydro-1H-carbazole and 1,2,3,4-tetrahydro-cyclopenta[b]indole derivatives as non-nucleoside inhibitors of hepatitis C virus NS5B RNA-dependent RNA polymerase. Bioorganic & medicinal chemistry letters 20060501
Synthesis and SAR of substituted tetrahydrocarbazole derivatives as new NPY-1 antagonists. Bioorganic & medicinal chemistry letters 20060315
1,2,3,4-tetrahydrocarbazoles as 5-HT6 serotonin receptor ligands. Bioorganic & medicinal chemistry letters 20040419
Properties