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942-01-8,MFCD00004959
Catalog No.:AA003D7F

942-01-8 | 1,2,3,4-Tetrahydrocarbazole

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5g
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$6.00   $4.00
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10g
98%
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$7.00   $5.00
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25g
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$16.00   $11.00
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100g
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  • Technical Information
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003D7F
Chemical Name:
1,2,3,4-Tetrahydrocarbazole
CAS Number:
942-01-8
Molecular Formula:
C12H13N
Molecular Weight:
171.2383
MDL Number:
MFCD00004959
SMILES:
C1CCc2c(C1)[nH]c1c2cccc1
NSC Number:
17329
Properties
Properties
 
BP:
325-330°C at 760 mmHg  
Form:
Solid  
MP:
118-120 °C  
Refractive Index:
1.6544 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
190  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Donor Count:
1  
Undefined Atom Stereocenter Count:
1  
XLogP3:
3.3  

Literature

Title: Enantioselective synthesis of spiro cyclopentane-1,3'-indoles and 2,3,4,9-tetrahydro-1H-carbazoles by iridium-catalyzed allylic dearomatization and stereospecific migration.

Journal: Angewandte Chemie (International ed. in English) 20120213

Title: Synthesis of 9-substituted 2,3,4,9-tetrahydro-1H-carbazole derivatives and evaluation of their anti-prion activity in TSE-infected cells.

Journal: European journal of medicinal chemistry 20111101

Title: 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.

Journal: The Journal of organic chemistry 20110107

Title: Potent and highly selective DP1 antagonists with 2,3,4,9-tetrahydro-1H-carbazole as pharmacophore.

Journal: Bioorganic & medicinal chemistry letters 20101215

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: One-pot synthesis of new substituted 1,2,3,4-tetrahydrocarbazoles via Petasis reaction.

Journal: Journal of combinatorial chemistry 20100913

Title: An enantioselective approach to highly substituted tetrahydrocarbazoles through hydrogen bonding-catalyzed cascade reactions.

Journal: Organic letters 20100305

Title: Derivatization of bioactive carbazoles by the biphenyl-degrading bacterium Ralstonia sp. strain SBUG 290.

Journal: Applied microbiology and biotechnology 20090501

Title: Synthesis and in-vitro antitumor activities of some mannich bases of 9-alkyl-1,2,3,4-tetrahydrocarbazole-1-ones.

Journal: Archiv der Pharmazie 20090301

Title: Indole and its alkyl-substituted derivatives protect erythrocyte and DNA against radical-induced oxidation.

Journal: Journal of biochemical and molecular toxicology 20090101

Title: 2,3,4,9-Tetra-hydro-1H-carbazole.

Journal: Acta crystallographica. Section E, Structure reports online 20081201

Title: The energetics of tetrahydrocarbazole aromatization over Pd(111): a computational analysis.

Journal: The Journal of chemical physics 20080314

Title: Binding of methoxy-substituted N1-benzenesulfonylindole analogs at human 5-HT6 serotonin receptors.

Journal: Bioorganic & medicinal chemistry letters 20060715

Title: 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.

Journal: Bioorganic & medicinal chemistry letters 20060501

Title: Synthesis and SAR of substituted tetrahydrocarbazole derivatives as new NPY-1 antagonists.

Journal: Bioorganic & medicinal chemistry letters 20060315

Title: 1,2,3,4-tetrahydrocarbazoles as 5-HT6 serotonin receptor ligands.

Journal: Bioorganic & medicinal chemistry letters 20040419

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