16732-70-0
16732-70-0
Chemical Structure
2-(Ethoxycarbonyl)-5-bromo-indole
- CAS No.: 16732-70-0
- Formula:C11H10BrNO2
- Molecular Weight:268.11
IUPAC Name: Ethyl 5-bromo-1H-indole-2-carboxylate
InChIKey: LWRLKENDQISGEU-UHFFFAOYSA-N
SMILES: O=C(C(N1)=CC2=C1C=CC(Br)=C2)OCC
Biological Activity: Ethyl 5-bromo-1H-indole-2-carboxylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2-(Ethoxycarbonyl)-5-bromo-indole | 99.92% | Ethyl 5-bromo-1H-indole-2-carboxylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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eIF4A3-IN-8 | 99.93% | eIF4A3-IN-8 serves as a negative control targeting eukaryotic initiation factor 4A3 (eIF4A3), with an IC50 > 100 μM; it exhibits no significant activity. | ||||||||||||||||||||
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Ethyl indole-2-carboxylate | 2-Carbethoxyindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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Indole-2-carboxylic acid (Standard) | 99.78% | Indole-2-carboxylic acid (Standard) is the analytical standard of Indole-2-carboxylic acid. This product is intended for research and analytical applications. Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current. | ||||||||||||||||||||
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Indole-2-carboxylic acid-13C | Indole-2-carboxylic acid-13C is the 13C-labeled Indole-2-carboxylic acid. Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. Indole-2-carboxylic acid (I2CA) specifically and competitively inhibits the potentiation by glycine of NMDA-gated current. | |||||||||||||||||||||
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Ethyl 6-bromo-1H-indole-3-carboxylate | 97.48% | Ethyl 6-bromo-1H-indole-3-carboxylate is a marine-derived natural product with anti-tumor activity. Ethyl 6-bromo-1H-indole-3-carboxylate was isolated from the sponge Iotrochota purpurea collected in Indonesia. The structure of Ethyl 6-bromo-1H-indole-3-carboxylate was confirmed by spectroscopic methods and accurate mass measurements. | ||||||||||||||||||||
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5-Bromo-1H-indole-2-carboxylic acid | 99.67% | 5-Bromo-1H-indole-2-carboxylic acid is an indole-derived organic compound substituted with bromine and carboxyl groups. 5-Bromo-1H-indole-2-carboxylic serves as an important intermediate for the synthesis of other active compounds. | ||||||||||||||||||||
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Ethyl 1H-indole-3-carboxylate (Standard) | ≥98% | Ethyl 1H-indole-3-carboxylate (Standard) is the analytical standard of Ethyl 1H-indole-3-carboxylate. This product is intended for research and analytical applications. | ||||||||||||||||||||
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6-Chloroindole-2-carboxylic acid | 99.95% | 6-Chloroindole-2-carboxylic acid (Compound 10g) is a derivative of 2-carboxyindole. 6-Chloroindole-2-carboxylic acid can bind to the hepatitis C virus NS3 protease/NS4A cofactor complex, and its KD value for the ns4a-ns3p protein is 0.4 mM. | ||||||||||||||||||||
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Methyl 2-(6-bromo-1H-indol-3-yl)acetate | 99.37% | Methyl 2-(6-bromo-1H-indol-3-yl)acetate is a natural product derived from marine sources, specifically isolated from Pseudosuberites hyalinus. | ||||||||||||||||||||
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Methyl 6-bromo-1H-indole-3-carboxylate | 98.18% | Methyl 6-bromo-1H-indole-3-carboxylate is a marine-derived natural product with anti-tumor activity. Methyl 6-bromo-1H-indole-3-carboxylate exhibits growth inhibitory effects against Staphylococcus epidermidis. Methyl 6-bromo-1H-indole-3-carboxylate can be used in research related to Staphylococcus epidermidis infection and cancer. | ||||||||||||||||||||
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