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关于此项目
经验公式(希尔记法):
C8H11N
化学文摘社编号:
分子量:
121.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
108853
Assay:
98%
Form:
solid
Quality Level
assay
98%
form
solid
mp
53-57 °C (lit.)
storage temp.
2-8°C
SMILES string
C1CCc2[nH]ccc2C1
InChI
1S/C8H11N/c1-2-4-8-7(3-1)5-6-9-8/h5-6,9H,1-4H2
InChI key
KQBVVLOYXDVATK-UHFFFAOYSA-N
General description
4,5,6,7-Tetrahydroindoles, due to their easy aromatization, are good intermediates to synthesize indoles. 4,5,6,7-Tetrahydroindole on condensation with cyanoacetate leads to 1-ethylthio-2-cyano-4,5,6,7-tetrahydrocyclohexa-[c]-3H-pyrrolizin-3-one.
Application
4,5,6,7-Tetrahydroindole was used as reactant in:
- synthesis of ethyl 3-(4,5,6,7-tetrahydroindol-2-yl)-2-propynoate
- preparation of BODIPY dyes
- N-alkylation with chloromethyloxirane
- preparation of hydroindolepropynoate by chemo- and regioselective solvent-free ethynylation
- palladium- and copper-free cross-coupling of halopropynoates
- preparation of carbonylalkenyl indoles via coupling with dicarbonyl compounds
- 1:2 annelation of 4,5,6,7-tetrahydroindole with 1-benzoyl-2-phenylacetylene
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Sobenina, L. N.; et al.
Khim. Geterotsikl. Soedin., 39, 1113-1113 (2003)
Pyrrole-2-dithiocarboxylates: Synthesis of 2-(1-Alkylthio-2-cyanoethenyl) pyrroles.
Sobenina LN, et al.
Tetrahedron, 51(14), 4223-4230 (1995)
Arcadi, A.; et al.
Advanced Synthesis & Catalysis, 348, 331-331 (2006)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 324906-1G | 04061826732427 |
