1260610-79-4 Usage
Uses
Used in Pharmaceutical Industry:
Tert-butyl (4R)-4-(bromomethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate is utilized as a reagent for the synthesis of pharmaceutical compounds. Its unique structure allows for the creation of various functionalized oxazolidines, which are integral in the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, tert-butyl (4R)-4-(bromomethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate serves as a precursor for the production of agrochemicals. The synthesized oxazolidines can be tailored for use in pesticides or other agricultural chemicals, enhancing crop protection and yield.
Used in Materials Science:
Tert-butyl (4R)-4-(bromomethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate is employed as a building block in materials science. The synthesized oxazolidines can be incorporated into polymers or other materials to impart specific properties, such as improved mechanical strength or thermal stability.
Used in Organic Synthesis:
As a key reagent in organic synthesis, tert-butyl (4R)-4-(bromomethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate is used for the preparation of complex organic compounds. Its versatility in forming various functionalized oxazolidines makes it a valuable tool for chemists in creating novel molecules with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1260610-79-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,6,1 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1260610-79:
(9*1)+(8*2)+(7*6)+(6*0)+(5*6)+(4*1)+(3*0)+(2*7)+(1*9)=124
124 % 10 = 4
So 1260610-79-4 is a valid CAS Registry Number.
1260610-79-4Relevant academic research and scientific papers
Mahler, Graciela,Serra, Gloria,Manta, Eduardo
, p. 1481 - 1492 (2005)
Starting from L-aminoacids, facile methods for the preparation 2-aminocta-4,7-dien-ol with different stereochemistry have been developed as key intermediates of mycothiazole and analogs. Copyright Taylor & Francis, Inc.
