4276-85-1 Usage
Uses
Used in Pharmaceutical Industry:
2,4,6-Triisopropylphenylacetic acid is used as an intermediate for the synthesis of various pharmaceutical products. Its unique structure and properties make it a valuable building block in the development of active pharmaceutical ingredients, contributing to the creation of new and effective medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4,6-Triisopropylphenylacetic acid is utilized as an intermediate in the synthesis of various agrochemical products. Its role in the production of these compounds helps to enhance crop protection and improve agricultural yields.
Used in Organic Compounds Synthesis:
2,4,6-Triisopropylphenylacetic acid is employed as a building block in the synthesis of other organic compounds. Its unique structure allows for the creation of a wide range of organic molecules, expanding the possibilities for chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 4276-85-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4276-85:
(6*4)+(5*2)+(4*7)+(3*6)+(2*8)+(1*5)=101
101 % 10 = 1
So 4276-85-1 is a valid CAS Registry Number.
4276-85-1Relevant academic research and scientific papers
Oxidation of Alkynyl Boronates to Carboxylic Acids, Esters, and Amides
Li, Chenchen,Li, Ruoling,Zhang, Bing,Zhao, Pei,Zhao, Wanxiang
supporting information, p. 10913 - 10917 (2020/05/25)
A general efficient protocol was developed for the synthesis of carboxylic acids, esters, and amides through oxidation of alkynyl boronates, generated directly from terminal alkynes. This protocol represents the first example of C(sp)?B bond oxidation. This approach displays a broad substrate scope, including aryl and alkyl alkynes, and exhibits excellent functional group tolerance. Water, primary and secondary alcohols, and amines are suitable nucleophiles for this transformation. Notably, amino acids and peptides can be used as nucleophiles, providing an efficient method for the synthesis and modification of peptides. The practicability of this methodology was further highlighted by the preparation of pharmaceutical molecules.
