1 2 3 4-TETRAHYDROCYCLOPENT(B) INDOLE manufacturers
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| | 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）;1,2,3,4-Tetrahydrocyclopent[b] indole | | CAS: | 2047-91-8 | | MF: | C11H11N | | MW: | 157.21 | | EINECS: | | | Product Categories: | Building Blocks;Heterocyclic Building Blocks;Indoles;Building Blocks;C11;Chemical Synthesis;Heterocyclic Building Blocks | | Mol File: | 2047-91-8.mol |  |
| | 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.) | | InChI | 1S/C11H11N/c1-2-6-10-8(4-1)9-5-3-7-11(9)12-10/h1-2,4,6,12H,3,5,7H2 | | InChIKey | HZDXFZHFEASSBM-UHFFFAOYSA-N | | SMILES | C1Cc2[nH]c3ccccc3c2C1 |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | HS Code | 2933.99.9701 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | 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. |
| | 1 2 3 4-TETRAHYDROCYCLOPENT(B) INDOLE Preparation Products And Raw materials |
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