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关于此项目
经验公式(希尔记法):
C10H9NO2
化学文摘社编号:
分子量:
175.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
141826
Assay:
99%
Form:
solid
assay
99%
form
solid
mp
68-71 °C (lit.)
functional group
ester
SMILES string
COC(=O)c1cccc2[nH]ccc12
InChI
1S/C10H9NO2/c1-13-10(12)8-3-2-4-9-7(8)5-6-11-9/h2-6,11H,1H3
InChI key
WEAXQUBYRSEBJD-UHFFFAOYSA-N
General description
The IR and UV spectra of methyl indole-4-carboxylate was studied.
Application
- Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
- Reactant for preparation of cytotoxic agents against multidrug-resistant cancer cells
- Reactant for preparation of inhibitor for β-tryptase
- Reactant for preparation of histamine H3 antagonists
- Reactant for preparation of JNK3 MAP kinase inhibitors
- Reactant for preparation of nucleosides
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
Isocarbostyrils. II. The Conversion of 2-Methyl-4-acyl-5-nitroisocarbostyrils to 2-Substituted Indole-4-carboxylic Acids.
Canadian Journal of Chemistry, 49(17), 2797-2802 (1971)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 273880-1G | 04061826135945 |
