CAS 610-04-8

3-Formylsalicylic acid

Description:

3-Formylsalicylic acid, with the CAS number 610-04-8, is an organic compound that features both an aldehyde and a carboxylic acid functional group, making it a member of the salicylic acid derivatives. It is characterized by its aromatic structure, which includes a hydroxyl group and a formyl group positioned at the 3 and 1 positions of the benzene ring, respectively. This compound typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and ethanol. Its chemical properties allow it to participate in various reactions, including condensation and esterification, making it useful in organic synthesis and medicinal chemistry. Additionally, 3-formylsalicylic acid may exhibit biological activity, which has drawn interest for potential applications in pharmaceuticals. The compound's reactivity and functional groups contribute to its versatility in chemical reactions, making it a valuable intermediate in the synthesis of more complex molecules.

Formula: C₈H₆O₄

InChI: InChI=1S/C8H6O4/c9-4-5-2-1-3-6(7(5)10)8(11)12/h1-4,10H,(H,11,12)

InChI key: InChIKey=YOEUNKPREOJHBW-UHFFFAOYSA-N

SMILES: C(O)(=O)C1=C(O)C(C=O)=CC=C1

Synonyms:

• 2-Hydroxyisophthalaldehydic acid
• 3-Aldehydesalicylic acid
• 3-Carboxy-2-hydroxybenzaldehyde
• 3-Carboxysalicylaldehyde
• 3-Formylsalicylic Acid
• Benzoic acid, 3-formyl-2-hydroxy-
• Isophthalaldehydic acid, 2-hydroxy-
• NSC 55753
• 3-Formyl-2-hydroxybenzoic acid
• 3-Formyl-2-hydroxybenzoic acid

3-FORMYLSALICYLIC ACID, 97

CAS: 610-04-8

Formula: C₈H₆O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 166.1308

Ref: IN-DA00EIIZ

3-Formyl-2-hydroxybenzoic acid

CAS: 610-04-8

3-Formyl-2-hydroxybenzoic acid

Purity: 98%

Molecular weight: 166.13g/mol

Ref: 54-OR510243

3-Formyl-2-hydroxybenzoic acid

CAS: 610-04-8

Purity: 98%

Molecular weight: 166.1320038

Ref: 10-F788252

3-Formyl-2-hydroxybenzoic acid

CAS: 610-04-8

3-Formyl-2-hydroxybenzoic acid is a compound that belongs to the class of 5-nitrosalicylic acid derivatives. It is used as an intermediate in organic synthesis. 3-Formyl-2-hydroxybenzoic acid can be synthesized by reacting ethylene diamine with sodium carbonate and hydrochloric acid. The product can be purified by precipitating it from solution with excess sodium carbonate and then filtering off any insoluble impurities. 3-Formyl-2-hydroxybenzoic acid has been shown to have a matrix effect on the hydrogen bonding interactions between nitrogen atoms and other molecules, which may be due to its ability to act as a hydrogen bond donor or acceptor. This chemical's surface methodology has also been studied using gravimetric analysis, which is useful for determining the amount of 3-formyl-2-hydroxybenzoic acid present in a sample.

Formula: C₈H₆O₄

Purity: Min. 95%

Molecular weight: 166.1 g/mol

Ref: 3D-AAA61004

3-Formylsalicylic Acid

CAS: 610-04-8

3-Formylsalicylic acid acts as a non-competitive inhibitor of estrone sulfatase, with IC50 and Ki values of 150 nM and 120 nM, respectively, inhibiting the enzyme responsible for converting estrone sulfate into estrone. Additionally, this compound is utilized in the synthesis of Schiff bases.

Formula: C₈H₆O₄

Color and Shape: Solid

Molecular weight: 166.132

Ref: TM-T85182