Ethyl 2-chloro-5-nitrobenzoate is an organic compound characterized by its ester functional group, which is derived from benzoic acid. It features a chloro substituent and a nitro group on the aromatic ring, specifically at the 2 and 5 positions, respectively. This compound typically appears as a yellow to light brown solid or liquid, depending on its purity and form. It is known for its moderate solubility in organic solvents such as ethanol and dichloromethane, while being less soluble in water due to its hydrophobic aromatic structure. Ethyl 2-chloro-5-nitrobenzoate is often utilized in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals, owing to its reactivity and ability to undergo nucleophilic substitution reactions. Safety considerations include handling it with care, as it may pose risks such as skin and eye irritation, and it should be stored in a cool, dry place away from incompatible substances.

ethyl 2-chloro-5-nitrobenzoate

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The crystalline structure of ethyl 2-chloro-5-nitrobenzoate is a five-membered ring with two nitro groups. It is an organic compound that is used in the synthesis of other compounds. Ethyl 2-chloro-5-nitrobenzoate has a molecule weight of 154.06 g/mol, with a melting point of 64 °C and boiling point of 176 °C. The crystal structure is oriented and it has a dihedral angle of 90°. This compound has been shown to form hydrogen bonds with the carboxylate group and nitro groups, as well as being able to form a carboxylate group by removing the chlorine atom from the chloroethyl group, which can be replaced by another substituent. Ethyl 2-chloro-5-nitrobenzoate also has centroid coordinates (-0.6, -1.2).

CAS 16588-17-3: ethyl 2-chloro-5-nitrobenzoate

Ethyl2-chloro-5-nitrobenzoate

Ref: 3D-FE149868

Ethyl 2-Chloro-5-nitrobenzoate

Ref: 10-F066837

Benzoic acid, 2-chloro-5-nitro-, ethyl ester

Ref: IN-DA001WDU

Ethyl 2-chloro-5-nitrobenzoate

Ref: 54-OR21154