37891-93-3 Usage
Description
[(4-Methylphenyl)sulfonyl]methyltrifluoromethanesulfonate, commonly referred to as "Mitsunobu reagent," is a potent and adaptable chemical reagent utilized in the realm of organic synthesis. It is renowned for its proficiency in facilitating the formation of carbon-phosphorus, carbon-sulfur, and carbon-nitrogen bonds, thereby establishing its significance in the development of pharmaceuticals and agrochemicals. This reagent is particularly esteemed for its capacity to induce the inversion of stereochemistry in reactions, a feature that is indispensable for the production of chiral compounds. Furthermore, it is celebrated for its high selectivity and the gentle reaction conditions it necessitates, making it a favored option for numerous researchers in the domain of organic chemistry.
Uses
Used in Pharmaceutical Industry:
[(4-Methylphenyl)sulfonyl]methyltrifluoromethanesulfonate is used as a synthetic reagent for the creation of various pharmaceutical compounds. Its ability to form carbon-phosphorus, carbon-sulfur, and carbon-nitrogen bonds makes it a valuable tool in the synthesis of complex molecules, contributing to the development of novel drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, [(4-Methylphenyl)sulfonyl]methyltrifluoromethanesulfonate is employed as a synthetic reagent for the production of agrochemicals. Its versatility in bond formation aids in the synthesis of a wide range of agrochemical products, including pesticides and fertilizers, enhancing agricultural productivity and crop protection.
Used in Chiral Compound Synthesis:
[(4-Methylphenyl)sulfonyl]methyltrifluoromethanesulfonate is used as a stereochemistry reagent for the synthesis of chiral compounds. Its unique ability to promote the inversion of stereochemistry in reactions is crucial for the production of enantiomerically pure compounds, which are essential in various applications, including pharmaceuticals and materials science.
Used in Organic Chemistry Research:
As a research reagent, [(4-Methylphenyl)sulfonyl]methyltrifluoromethanesulfonate is utilized by scientists and researchers in the field of organic chemistry. Its high selectivity and mild reaction conditions make it a preferred choice for conducting various chemical reactions and experiments, furthering the understanding of chemical processes and the development of new synthetic methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 37891-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,9 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37891-93:
(7*3)+(6*7)+(5*8)+(4*9)+(3*1)+(2*9)+(1*3)=163
163 % 10 = 3
So 37891-93-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9F3O5S2/c1-7-2-4-8(5-3-7)18(13,14)6-17-19(15,16)9(10,11)12/h2-5H,6H2,1H3
