Description
4-[3-(Acryloyloxy)propoxy]benzoic acid (CAS No. 245349-46-6) is a high-purity benzoic acid derivative designed for advanced research and industrial applications. With the molecular formula C13H14O5 and IUPAC name 4-(3-prop-2-enoyloxypropoxy)benzoic acid, this compound features a reactive acrylate group and a benzoic acid moiety, making it ideal for polymer synthesis, photochemistry, and material science. Its precise structure enables controlled functionalization in crosslinking reactions, surface modifications, and specialty coatings. Packaged under inert conditions to ensure stability, this product is rigorously tested for purity (≥95% by HPLC) and consistency, meeting the demands of pharmaceutical, optoelectronic, and nanotechnology research.
Properties
- CAS Number: 245349-46-6
- Complexity: 292
- IUPAC Name: 4-(3-prop-2-enoyloxypropoxy)benzoic acid
- InChI: InChI=1S/C13H14O5/c1-2-12(14)18-9-3-8-17-11-6-4-10(5-7-11)13(15)16/h2,4-7H,1,3,8-9H2,(H,15,16)
- InChI Key: AHBWYWGJQFTBRO-UHFFFAOYSA-N
- Exact Mass: 250.08412354
- Molecular Formula: C13H14O5
- Molecular Weight: 250.25
- SMILES: C=CC(=O)OCCCOC1=CC=C(C=C1)C(=O)O
- Topological: 72.8
- Monoisotopic Mass: 250.08412354
- Synonyms: 245349-46-6, 4-[3-(Acryloyloxy)propoxy]benzoic acid, 4-(3-(acryloyloxy)propoxy)benzoic acid, 4-(3-prop-2-enoyloxypropoxy)benzoic acid, Benzoic acid, 4-[3-[(1-oxo-2-propen-1-yl)oxy]propoxy]-, SCHEMBL222350, DTXSID40595041, AHBWYWGJQFTBRO-UHFFFAOYSA-N, MFCD09753048, 4-(3-acryloyloxypropyloxy)-benzoic acid, G67641
Application
This acrylate-functionalized benzoic acid derivative serves as a versatile building block in photoactive polymers, liquid crystal displays (LCDs), and self-assembled monolayers (SAMs). It is particularly useful in UV-curable coatings, dental resins, and adhesives due to its crosslinking capability. Researchers also employ it in organic synthesis for introducing carboxylic acid handles in advanced materials.
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