1648864-26-9 Usage
Description
(R)-tert-butyl-3-(2-(tosyloxy)ethoxy)pyrrolidine-1-carboxylate is a chemical compound belonging to the class of pyrrolidine carboxylate esters. It is characterized by a molecular formula of C17H27NO6S and a molecular weight of 381.46 g/mol. This chiral compound features a stereocenter at the tert-butyl carbon and exists as a single enantiomer. The tosyl group in its structure acts as a leaving group in organic reactions, which makes it a valuable intermediate for a range of organic synthesis processes. It is widely recognized for its significance in the chemical and pharmaceutical industries.
Uses
Used in Pharmaceutical Synthesis:
(R)-tert-butyl-3-(2-(tosyloxy)ethoxy)pyrrolidine-1-carboxylate is used as an intermediate in the synthesis of pharmaceuticals. Its unique structure and reactivity contribute to the development of new drugs and medications, enhancing the diversity and effectiveness of available treatments.
Used in Organic Chemical Synthesis:
In the field of organic chemistry, (R)-tert-butyl-3-(2-(tosyloxy)ethoxy)pyrrolidine-1-carboxylate serves as a versatile intermediate for the synthesis of various organic chemicals. Its utility in creating complex molecular structures makes it a valuable asset in the development of novel compounds with potential applications in different industries.
Used in Chiral Compounds Production:
Due to its chiral nature, (R)-tert-butyl-3-(2-(tosyloxy)ethoxy)pyrrolidine-1-carboxylate is used in the production of chiral compounds. Chiral compounds are essential in various applications, including the creation of enantiomerically pure pharmaceuticals, which can have significant implications for drug efficacy and safety.
Used in Research and Development:
(R)-tert-butyl-3-(2-(tosyloxy)ethoxy)pyrrolidine-1-carboxylate is also utilized in research and development settings, where it can be employed to study the properties and behavior of chiral molecules, as well as to develop new methodologies and techniques in organic synthesis. Its unique characteristics make it an important tool for advancing scientific knowledge and innovation in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1648864-26-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,8,8,6 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1648864-26:
(9*1)+(8*6)+(7*4)+(6*8)+(5*8)+(4*6)+(3*4)+(2*2)+(1*6)=219
219 % 10 = 9
So 1648864-26-9 is a valid CAS Registry Number.
1648864-26-9Relevant articles and documents
SERINE/THREONINE KINASE INHIBITORS
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Paragraph 0283; 0284, (2015/02/19)
Compounds having the formula I wherein R1, R2, R3, R4, R5, Ra, Rb, Rc, Rd, Re, n, r, s and t are as defined herein and which compounds are inhibitors of PAK1. Also disclosed are compositions and methods for treating cancer and hyperproliferative disorders.
