20139-92-8

Usage

Uses

Used in Agriculture and Horticulture:
9-Anthraceneacetic acid Methyl ester is used as a plant growth regulator for enhancing plant growth and development. It is particularly effective in the propagation of plant cuttings, where it stimulates root formation, and in managing overall plant growth.
Used in Organic Synthesis:
In the field of organic chemistry, 9-Anthraceneacetic acid Methyl ester is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in creating complex organic molecules.
Used in Pharmaceutical Research:
9-Anthraceneacetic acid Methyl ester is also employed in pharmaceutical research as a potential precursor for the development of new drugs. Its chemical properties and interactions with biological systems are of interest to researchers seeking novel therapeutic agents.
It is crucial to handle 9-Anthraceneacetic acid Methyl ester with care due to its potential health hazards if not used properly, emphasizing the need for safety precautions in its application across industries.

InChI:InChI=1/C17H14O2/c1-19-17(18)11-16-14-8-4-2-6-12(14)10-13-7-3-5-9-15(13)16/h2-10H,11H2,1H3

Upstream product

• 186581-53-3 diazomethane 
• 6624-23-3 9-anthrylacetic acid 
• 67-56-1 methanol 

Relevant academic research and scientific papers

Electrostatic Control of Regioselectivity in Competing Biomolecular Eliminations

The isomeric trans-11,12-dichloro-9,10-dihydro-9,10-ethano-1-anthroic acids (1 and 2) have been prepared and characterized.Base-induced dehydrochlorinations of these and the corresponding cis-dichloroethano derivatives 3 and 4 were conducted under several sets of base/solvent conditions.Preparations and dehydrochlorinations of 2-ethanoic acid (15) and the corresponding cis-dichloro isomer 16 are also reported.Regioselectivities in vinyl halide formations are highest with K+O--t-Bu/t-BuOH/18 crown-6, conditions under which ion aggregation is minimized.The results of these studies indicate that both the syn and quasi-anti eliminations possess some carbanionic character but with most of the charge remaining on the attacking base in the transition states.

Factors influencing orientations of covalently-attached and doped aromatic groups in stretched polyethylene films

Linear polarizations have been measured for covalently attached and doped 9-anthryl and 1-pyrenyl groups residing in interior sites of stretched polyolefinic films. The influences of polymer crystallinity, the concentration of aromatic groups and the length of the substituents attached to doped molecules or of the tethers to polymer chains of covalently attached species on the degree of polarization have been explored. The results demonstrate the utility of comparing orientational parameters from doped and covalently attached groups in analyzing the factors responsible for stretch-induced orientation. The anthryl and pyrenyl groups prefer to reside in interfacial regions more than amorphous regions even before film stretching, and the specificity of their orientations is determined by the nature of interactions with surrounding polymer chains. The magnitudes of orientation factors are dependent on polymer crystallinity and substituent or tether length, but are independent of aromatic group concentrations as long as they are low. There are significant differences between the orientations of doped and covalently attached groups of the same type due to the inability of the latter to translocate between site types during film stretching. The results, as interpreted in the context of current theories, demonstrate the necessity of crystallite surfaces (i.e., interfacial sites), but not stretching-induced translocation, for selective orientation of aromatic groups along the axis of stretching.