CAS 58588-59-3

Benzoic acid, 3-chloro-4-formyl-

Description:

Benzoic acid, 3-chloro-4-formyl- (CAS 58588-59-3) is an aromatic carboxylic acid characterized by the presence of a benzoic acid moiety with a chloro substituent at the meta position and a formyl group at the para position relative to the carboxylic acid group. This compound typically appears as a white to off-white solid and is soluble in organic solvents, reflecting its aromatic structure. The presence of the chloro and formyl groups introduces reactivity, making it useful in various chemical syntheses, particularly in the production of pharmaceuticals and agrochemicals. Its functional groups allow for electrophilic substitution reactions and can participate in condensation reactions. The compound's properties, such as melting point and boiling point, are influenced by its molecular structure and the interactions between its functional groups. As with many chlorinated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns. Overall, benzoic acid, 3-chloro-4-formyl- is a versatile intermediate in organic synthesis.

Formula: C₈H₅ClO₃

Synonyms:

• 3-Chloro-4-formylbenzoic acid
• Benzoic acid, 3-chloro-4-formyl-

3-Chloro-4-formylbenzoic acid

CAS: 58588-59-3

Formula: C₈H₅ClO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 184.5765

Ref: IN-DA00EL47

3-Chloro-4-formylbenzoic acid

CAS: 58588-59-3

3-Chloro-4-formylbenzoic acid

Purity: 98%

Molecular weight: 184.58g/mol

Ref: 54-OR960323

3-CHLORO-4-FORMYLBENZOIC ACID

CAS: 58588-59-3

Formula: C₈H₅ClO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 184.58

Ref: 10-F390209

3-chloro-4-formylbenzoic acid

CAS: 58588-59-3

3-chloro-4-formylbenzoic acid is an aldehyde that can be used as a synthetic intermediate in the production of other molecules. It can be synthesized from 3-chlorobenzoic acid and formaldehyde in one step by heating the two together. This reaction produces the desired product in high yield, with a stereochemical purity of about 98%. The substituent on the chloro group has no effect on this reaction. The diastereoselectivity of this synthesis is also high, with nearly all products being racemic mixtures.

Formula: C₈H₅ClO₃

Purity: Min. 95%

Molecular weight: 184.6 g/mol

Ref: 3D-ICA58859