13922-41-3
Chemical Structure
1-Naphthaleneboronic acid
- CAS No.: 13922-41-3
- Formula:C10H9BO2
- Molecular Weight:171.99
IUPAC Name: naphthalen-1-ylboronic acid
InChIKey: HUMMCEUVDBVXTQ-UHFFFAOYSA-N
SMILES: OB(O)C1=C(C=CC=C2)C2=CC=C1
Biological Activity: 1-Naphthaleneboronic acid is a biochemical reagent that can serve as a starting material or reaction reagent for chemical synthesis. 1-Naphthaleneboronic acid mainly introduces its naphthalene ring into other scaffolds through Suzuki-Miyaura cross-coupling or Friedel-Crafts alkylation reactions, thereby synthesizing target products with specific functions such as fluorescence imaging, photodynamic therapy targeting, or affinity adsorption. 1-Naphthaleneboronic acid can be used in research on photosensitizers and the synthesis of hypercrosslinked polymers with boronic acid affinity[1][2][3][4][5][6][7][8][9].
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1-Naphthaleneboronic acid | 99.96% | 1-Naphthaleneboronic acid is a biochemical reagent that can serve as a starting material or reaction reagent for chemical synthesis. 1-Naphthaleneboronic acid mainly introduces its naphthalene ring into other scaffolds through Suzuki-Miyaura cross-coupling or Friedel-Crafts alkylation reactions, thereby synthesizing target products with specific functions such as fluorescence imaging, photodynamic therapy targeting, or affinity adsorption. 1-Naphthaleneboronic acid can be used in research on photosensitizers and the synthesis of hypercrosslinked polymers with boronic acid affinity. | ||||||||||||||||||||
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1-Naphthaleneboronic acid-d7 | 1-Naphthaleneboronic acid-d7 is the deuterated-labeled 1-Naphthaleneboronic acid (HY-78494). 1-Naphthaleneboronic acid is a biochemical reagent that can serve as a starting material or reaction reagent for chemical synthesis. 1-Naphthaleneboronic acid mainly introduces its naphthalene ring into other scaffolds through Suzuki-Miyaura cross-coupling or Friedel-Crafts alkylation reactions, thereby synthesizing target products with specific functions such as fluorescence imaging, photodynamic therapy targeting, or affinity adsorption. 1-Naphthaleneboronic acid can be used in research on photosensitizers and the synthesis of hypercrosslinked polymers with boronic acid affinity. | |||||||||||||||||||||
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References
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- [6]. Tan YJ, et al. Galloyl esters of trans-stilbenes are inhibitors of FASN with anticancer activity on non-small cell lung cancer cells. European journal of medicinal chemistry. 2019 Nov 15;182:111597. [Content Brief]
- [7]. Luo B, et al. A high-contrast mechano-induced blue-shift in triphenylacrylonitrile derivative crystals via exciton coupling disruption for advanced information encryption. Dyes and Pigments. 2026 Apr 28:113820.
- [8]. Negrete-Raymond AC, et al. Catabolism of arylboronic acids by Arthrobacter nicotinovorans strain PBA. Applied and environmental microbiology. 2003 Jul;69(7):4263-7.
- [9]. Singh S, et al. Discovery of a novel series of N-hydroxypyridone derivatives protecting astrocytes against hydrogen peroxide-induced toxicity via improved mitochondrial functionality. Bioorganic & medicinal chemistry. 2017 Feb 15;25(4):1394-1405. [Content Brief]
