6312-86-3 Usage
Uses
Used in Dye Manufacturing:
2-(3-nitrophenoxy)Benzoic acid is used as a key intermediate in the production of dyes, contributing to the coloration and stability of various dye formulations.
Used in Pharmaceutical Industry:
2-(3-nitrophenoxy)Benzoic acid is utilized as an active pharmaceutical ingredient, particularly for its anti-inflammatory properties. It is incorporated into topical ointments and creams to provide relief from inflammation and associated symptoms.
Used in Agricultural Chemicals:
In the agricultural sector, 2-(3-nitrophenoxy)Benzoic acid is employed in the development of agricultural chemicals, potentially enhancing crop protection and yield through its chemical properties.
It is crucial to handle 2-(3-nitrophenoxy)Benzoic acid with caution due to its potential hazards and toxic nature, ensuring safety in its application across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6312-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6312-86:
(6*6)+(5*3)+(4*1)+(3*2)+(2*8)+(1*6)=83
83 % 10 = 3
So 6312-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO5/c15-13(16)11-6-1-2-7-12(11)19-10-5-3-4-9(8-10)14(17)18/h1-8H,(H,15,16)
6312-86-3Relevant academic research and scientific papers
Efficient Aryl Migration from an Aryl Ether to a Carboxylic Acid Group To Form an Ester by Visible-Light Photoredox Catalysis
Wang, Shao-Feng,Cao, Xiao-Ping,Li, Yang
, p. 13809 - 13813 (2017/10/24)
We have developed a highly efficient aryl migration from an aryl ether to a carboxylic acid group through retro-Smiles rearrangement by visible-light photoredox catalysis at ambient temperature. Transition metals and a stoichiometric oxidant and base are avoided in the transformation. Inspired by the high efficiency of this transformation and the fundamental importance of C?O bond cleavage, we developed a novel approach to the C?O cleavage of a biaryl ether to form two phenolic compounds, as demonstrated by a one-pot, two-step gram-scale reaction under mild conditions. The aryl migration exhibits broad scope and can be applied to the synthesis of pharmaceutical compounds, such as guacetisal. Primary mechanistic studies indicate that the catalytic cycle occurs by a reductive quenching pathway.
