ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE
- Product Name
- ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE
- CAS No.
- 69404-00-8
- Chemical Name
- ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE
- Synonyms
- Ethyl-5-nitrobenzofuran-2-carboxilate;ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE;ETHYL 5-NITROBENZO[B]FURAN-2-CARBOXYLATE;Ethyl 5-nitrobenzofuran-2-carboxylate ,97%;5-nitro-2-benzofurancarboxylic acid ethyl ester;5-NITROBENZO[B]FURAN-2-CARBOXYLIC ACID ETHYL ESTER
- CBNumber
- CB0420002
- Molecular Formula
- C11H9NO5
- Formula Weight
- 235.19
- MOL File
- 69404-00-8.mol
ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE Property
- Melting point:
- 150-155 °C
Safety
- Safety Statements
- 24/25
- HS Code
- 29329990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P321Specific treatment (see … on this label).
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P362Take off contaminated clothing and wash before reuse.
N-Bromosuccinimide Price
- Product number
- B125053
- Product name
- Ethyl5-Nitro-1-benzofuran-2-carboxylate
- Packaging
- 50mg
- Price
- $75
- Updated
- 2021/12/16
ETHYL 5-NITROBENZOFURAN-2-CARBOXYLATE Chemical Properties,Usage,Production
Uses
Deriatives of benzofuran-2-carboxylic acid are known for exhibiting various pharmacological activities such as selective adenosine A2A receptor antagonists, anti-inflammatory agents and local anaesthetics. Benzofuran-2-carboxylic acids bearing benzoyl nitrogen such as Ethyl 5-Nitrobenzofuran-2-carboxylate, are used as DNA-binding groups, where the these structural subunits mimic natural antitumor agents such as duocarmycin and netropsin.