149609-84-7

Basic information

• Product Name: 3-((2-METHYLPROP-2-ENYL)OXY)BENZOIC ACID
• Synonyms: ZERENEX E/5016861;3-((2-METHYLPROP-2-ENYL)OXY)BENZOIC ACID;CHEMBRDG-BB 4023591;3-[(2-METHYLPROP-2-EN-1-YL)OXY]BENZOIC ACID;AKOS BBB/639;UKRORGSYN-BB BBV-080237;3-[(2-methylprop-2-en-1-yl)oxy]benzoic acid(SALTDATA: FREE)
• CAS NO: 149609-84-7
• Molecular Formula: C₁₁H₁₂O₃
• Molecular Weight: 192.21
• Mol File: 149609-84-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 340.755°C at 760 mmHg
• Flash Point: 133.398°C
• Appearance: /
• Density: 1.128g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.538
• PKA: 4.03±0.10(Predicted)
• CAS DataBase Reference: 3-((2-METHYLPROP-2-ENYL)OXY)BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-((2-METHYLPROP-2-ENYL)OXY)BENZOIC ACID(149609-84-7)
• EPA Substance Registry System: 3-((2-METHYLPROP-2-ENYL)OXY)BENZOIC ACID(149609-84-7)

Safety Data

• Hazardous Substances Data: 149609-84-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H12O3/c1-8(2)7-14-10-5-3-4-9(6-10)11(12)13/h3-6H,1,7H2,2H3,(H,12,13)

Upstream product

• 99-06-9 3-Carboxyphenol 
• 19438-10-9 methyl 3-hydroxybenzoate 
• 136954-98-8 3-<(2-methylprop-1-en-3-yl)oxy> benzoic acid methyl ester 
• 209256-57-5 ethyl 3-((2-methylallyl)oxy)benzoate 
• 7781-98-8 ethyl-3-hydroxybenzoate 

Relevant articles and documents

Sulfoximine-Assisted One-Pot Unsymmetrical Multiple Annulation of Arenes: A Combined Experimental and Computational Study

Discussed herein is an unprecedented Ru-catalyzed one-pot unsymmetrical C-H difunctionalization of arenes comprising intramolecular hydroarylation of olefins and intermolecular annulation of alkynes. This unprecedented 2-fold C-H functionalization is validated on the basis of experimental and density functional theory (DFT) study. The transformation readily occurs with the assistance of methylphenyl sulfoximine (MPS) directing group in the presence of Ru catalyst forming two C-C and one C-N bonds in a single operation. The overall process is atom economical and step-efficient and provides unusual dihydrofuran-fused isoquinolone heterocycles. Further annulation of NH and the proximal o-C-H-arene of isoquinolone with alkynes build highly conjugated novel polycyclic compounds. Overall, three independent annulations in arene motifs are visualized and thoughtfully executed; finally, 5 ring-fused structural entities are constructed forming three C-C and two C-N bonds.

Rh(iii)-Catalyzed intramolecular redox-neutral cyclization of alkenes via C-H activation

Biologically interesting fused oligocyclic lactams have been prepared via an intramolecular redox-neutral cyclization process. By the proper choice of the substrates with a wide variety of tethered olefins, the less favored C-H bond can be activated and f

ALLYLQXY AND ALKYLOXY BENZOIC ACID DELIVERY AGENTS

The present invention relates to pharmaceutical compounds for delivering active agents, such as biologically or chemically active agents, to a target. The invention also relates to pharmaceutical compositions comprising at least one delivery agent compound of the present invention and at least one active agent, and unit dosage forms comprising such compositions. Methods for the preparation and administration of the pharmaceutical compositions are also disclosed.