structure of 2-(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid

2-(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid

CAS No.: 1000414-37-8
M. Wt: 194.18400
M. Fa: C10H10O4
InChI Key: XGXRWHAYNFAHBM-UHFFFAOYSA-N
Appearance: light yellow solid

Names and Identifiers of 1000414-37-8

CAS Number

1000414-37-8

MDL Number

MFCD13184245

IUPAC Name

2-(6-hydroxy-2,3-dihydro-1-benzofuran-3-yl)acetic acid

InChI

InChI=1S/C10H10O4/c11-7-1-2-8-6(3-10(12)13)5-14-9(8)4-7/h1-2,4,6,11H,3,5H2,(H,12,13)

InChIKey

XGXRWHAYNFAHBM-UHFFFAOYSA-N

Canonical SMILES

C1C(C2=C(O1)C=C(C=C2)O)CC(=O)O

UNSPSC Code

12352100

Physical and chemical properties of 1000414-37-8

Exact Mass

194.05800

LogP

1.34290

Molecular Formula

C10H10O4

Molecular Weight

194.18400

PSA

66.76000

Storage condition

2-8°C

Safety Information of 1000414-37-8

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000414-37-8

This compound has a wide range of applications:

  • Medicinal Chemistry: It is investigated for potential therapeutic effects in treating various diseases.
  • Material Science: Used as a building block for synthesizing more complex molecules.
  • Biological Research: Studied for its antimicrobial and anticancer properties.

Biological Activity of 1000414-37-8

Research indicates that 2-(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid exhibits potential biological activities, including:

  • Antimicrobial properties: It has been studied for its ability to inhibit the growth of various microorganisms.
  • Anticancer effects: Preliminary studies suggest it may have cytotoxic effects against certain cancer cell lines.

The biological activity is attributed to its interaction with specific molecular targets, facilitated by the hydroxyl group and the benzofuran ring, which can influence enzyme activity and receptor binding.

Retrosynthesis analysis of 1000414-37-8

  • Route#1

    Cas:69716-04-7
    Cas:1000414-37-8