Basic information Safety Supplier Related

1 2 3 4-TETRAHYDROCYCLOPENT(B) INDOLE

Basic information Safety Supplier Related

1 2 3 4-TETRAHYDROCYCLOPENT(B) INDOLE Basic information

Product Name:
1 2 3 4-TETRAHYDROCYCLOPENT(B) INDOLE
Synonyms:
  • TETRAHYDROCYCLOPENT(B)INDOLE
  • 2,3-Trimethyleneindole
  • NSC 112674
  • 1,2,3,4-Tetrahydrocyclopent[b] indole 96%
  • 1,2,3,4-Tetrahydro cyclopenta indole
  • 1,2,3,4-Tetrahydrocyclopent[b] indole(NSC 112674)
CAS:
2047-91-8
MF:
C11H11N
MW:
157.21
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Indoles
  • Building Blocks
  • C11
  • Chemical Synthesis
  • Heterocyclic Building Blocks
Mol File:
2047-91-8.mol
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1 2 3 4-TETRAHYDROCYCLOPENT(B) INDOLE Chemical Properties

Melting point:
100.5-105.5 °C(lit.)
Boiling point:
160-162 °C(Press: 1 Torr)
Density 
1.200±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Chloroform, Methanol
form 
powder to crystaline
pka
17.83±0.20(Predicted)
color 
Light yellow to Brown
λmax
230nm(EtOH aq.)(lit.)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2933.99.9701
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1 2 3 4-TETRAHYDROCYCLOPENT(B) INDOLE Usage And Synthesis

Uses

• ;Reactant for thionium species-mediated functionalization at the 2α-position of indoles1• ;Reactant for preparation of tetramethylpiperidine-1-oxoammonium salts as oxidants2

Uses

1,2,3,4-Tetrahydrocyclopent[b]indole is used in the synthesis of BACE inhibitors. Also used to synthesize benzazocinecarboxylic acids as potential antiinflammatory agents.

Uses

  • Reactant for thionium species-mediated functionalization at the 2α-position of indoles
  • Reactant for preparation of tetramethylpiperidine-1-oxoammonium salts as oxidants

General Description

1,2,3,4-Tetrahydrocyclopent[b] indole undergoes reduction in the presence of Pd/C and hydrogen gas to yield 1,2,3,3a,4,8b-hexahydrocyclopent[b]indole.

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