77201-17-3

Basic information

• Product Name: Benzoic acid, 3-hydroxy-, butyl ester
• CAS NO: 77201-17-3
• Molecular Formula: C11H14O3
• Molecular Weight: 194.23
• Mol File: 77201-17-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3-hydroxy-, butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-hydroxy-, butyl ester(77201-17-3)
• EPA Substance Registry System: Benzoic acid, 3-hydroxy-, butyl ester(77201-17-3)

Safety Data

• Hazardous Substances Data: 77201-17-3(Hazardous Substances Data)

Upstream product

• 99-06-9 3-Carboxyphenol 
• 71-36-3 butan-1-ol 

Downstream Products

• 251640-56-9 N-[6-(3-hydroxy-3-methyl-1-butynyl)-2-pyridyl]-3-n-octoxybenzamide 
• 251640-58-1 N-(6-ethynyl-2-pyridyl)-3-n-octoxybenzamide 
• 251640-54-7 N-(6-bromo-2-pyridyl)-3-n-octoxybenzamide 
• 79785-45-8 3-(octyloxy)benzoic acid 
• 251640-52-5 n-butyl 3-n-octoxybenzoate 

Relevant articles and documents

Glucopyranoside recognition by polypyridine-macrocyclic receptors possessing a wide cavity with a flexible linkage

New polypyridine-macrocyclic receptors for glucopyranosides were designed and synthesized. The artificial receptors possess a terpyridine skeleton as a hydrogen-bonding site and a flexible polyoxyethylene chain as a bridge for the macrocyclic structure, in which the cavity of the receptors is large enough to incorporate pyranosides. The receptors showed high affinities for n-octyl ?2-(D)-glucopyranoside, and selective binding of the receptors was observed between epimeric pyranosides. The results obtained in this paper demonstrated versatility of the terpyridine skeleton as a hydrogenbonding site for saccharides.

Structure–activity relationships of vanillic acid ester analogs in inhibitory effect of antigen-mediated degranulation in rat basophilic leukemia RBL-2H3 cells

Methyl vanillate (1) showed strong degranulation inhibitory activity among vanillin derivatives tested. In order to find structure–activity relationships for developing anti-allergic agents with simple structures and potent activity, we synthesized several vanillic acid (VA) ester derivatives with C1–C4and C8alkyl chains and evaluated their degranulation inhibitory activities. The most active compound of VA ester derivatives was derivative 5 with a C4straight alkyl chain, and derivative 5 exhibited approximately three-fold greater inhibitory activity than that of 1. Moreover, we designed 8 types of analogs based on 5, and we found that the minimum structure for potent degranulation inhibitory activity requires direct connection of the butyl ester moiety on the benzene ring and at least one hydroxyl group on the benzene ring. Butyl meta or para hydroxyl benzoate (10 or 11) has a simpler structure than that of 5 and exhibited more potent degranulation inhibitory activity than that of 5.