901310-02-9 Usage
Uses
Used in Organic Synthesis:
2,6-Dibromo phenylacetic acid is used as a chemical intermediate in the production of various complex organic compounds. Its unique structure, with bromine atoms and a carboxylic acid group, makes it a valuable building block for synthesizing a wide range of organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-Dibromo phenylacetic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical properties allow for the development of new drugs with specific therapeutic effects.
Used in Agrochemical Industry:
2,6-Dibromo phenylacetic acid is also utilized in the agrochemical industry for the synthesis of active ingredients in pesticides and herbicides. Its ability to form complex organic compounds makes it a valuable component in the development of effective crop protection products.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 2,6-Dibromo phenylacetic acid is used as a starting material for the synthesis of various dyes and pigments. Its unique structure allows for the creation of dyes with specific color properties and stability.
Used in Research and Development:
2,6-Dibromo phenylacetic acid is employed in research and development laboratories for the exploration of new chemical reactions and the synthesis of novel organic compounds. Its unique properties make it an interesting subject for scientific investigation and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 901310-02-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,1,3,1 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 901310-02:
(8*9)+(7*0)+(6*1)+(5*3)+(4*1)+(3*0)+(2*0)+(1*2)=99
99 % 10 = 9
So 901310-02-9 is a valid CAS Registry Number.
901310-02-9Relevant academic research and scientific papers
An efficient one-pot synthesis of novel 4-aryl-1-methyloxindoles
van den Hoogenband, Adri,Lange, Jos H.M.,Iwema-Bakker, Wouter I.,den Hartog, Jack A.J.,van Schaik, Jord,Feenstra, Rolf W.,Terpstra, Jan Willem
, p. 4361 - 4364 (2007/10/03)
An unprecedented synthetic approach to novel 4-aryl-1-methyloxindoles is described. The method involves the intramolecular palladium-catalyzed amidation of N-methyl-2,6-dibromophenylacetamide followed by an in situ Suzuki cross-coupling reaction with a (h
