1701-77-5 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
Methoxy(phenyl)acetic acid is utilized as a key building block in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides. Its chemical structure allows for the creation of a wide range of compounds with potential therapeutic and pesticidal properties.
Used in Organic Chemistry as a Reagent:
In the realm of organic chemistry, methoxy(phenyl)acetic acid serves as a valuable reagent, particularly in the formation of esters and amides. Its ability to participate in these reactions facilitates the synthesis of diverse organic compounds, broadening its applications in research and industrial processes.
Used in Research and Development:
Methoxy(phenyl)acetic acid is employed in research and development settings to explore its potential applications and to understand its chemical properties. This includes investigating its reactivity, stability, and interactions with other compounds, which can lead to the discovery of new synthetic pathways and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1701-77-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1701-77:
(6*1)+(5*7)+(4*0)+(3*1)+(2*7)+(1*7)=65
65 % 10 = 5
So 1701-77-5 is a valid CAS Registry Number.
1701-77-5Relevant academic research and scientific papers
Resolution of (±)-mandelic- and (±)-2-(chiorophenoxy)propionic-acid derivatives by crystallization of their diastereomeric amides with (R)- or (S)-α-arylethylamines
Jourdain, Franck,Hirokawa, Takahiko,Kogane, Tamizo
, p. 2509 - 2512 (2007/10/03)
An alternative and cost effective route for the resolution in high ees (95-99%) of (±)-mandelic-and (±)-2-(chlorophenoxy)propionic- acid derivatives is reported. The key step involves the covalent derivatization and separation of their diastereomeric amides with (R)- or (S)-α- arylethylamines.
Direct Optical Resolution of Carboxylic Acids by Chyral HPLC on Tris(3,5-dimethylphenylcarbamate)s of Cellulose and Amylose
Okamoto, Yoshio,Aburatani, Ryo,Kaida, Yuriko,Hatada, Koichi
, p. 1125 - 1128 (2007/10/02)
A variety of racemic carboxylic acids have been for the first time directly resolved by normal-phase, high-performance liquid chromatography using a hexane-2-propanol eluting system containing a small amount (ca. 1percent) of a strong carboxylic acid, like formic acid, trichloroacetic acid, and trifluoroacetic acid.
