1581734-69-1 Usage
Description
(2R,3S)-1-benzyl 4-tert-butyl 3-(cyclopropylmethyl)-2-(3,3,3-5 trifluoropropyl)succinate is a complex chiral organic compound characterized by its unique molecular structure. It features a succinate backbone with various substituent groups, including benzyl, tert-butyl, cyclopropylmethyl, and trifluoropropyl groups. The (2R,3S) designation indicates the specific spatial arrangement of these substituents around the central carbon atoms, which is crucial for its properties and potential applications.
Uses
Used in Organic Synthesis:
(2R,3S)-1-benzyl 4-tert-butyl 3-(cyclopropylmethyl)-2-(3,3,3-5 trifluoropropyl)succinate is used as a building block in organic synthesis for the creation of more complex molecules. The presence of benzyl and tert-butyl groups allows for versatile synthetic manipulations, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Chemistry:
In the pharmaceutical industry, (2R,3S)-1-benzyl 4-tert-butyl 3-(cyclopropylmethyl)-2-(3,3,3-5 trifluoropropyl)succinate is used as a key intermediate in the development of new drugs. Its chiral nature and diverse functional groups enable the design of enantioselective catalysts and ligands, which are essential for the synthesis of biologically active compounds with high selectivity and potency.
Used in Industrial Applications:
The unique combination of fluorinated and cyclopropylmethyl groups in (2R,3S)-1-benzyl 4-tert-butyl 3-(cyclopropylmethyl)-2-(3,3,3-5 trifluoropropyl)succinate may confer specific chemical properties that are valuable in various industrial applications. These could include uses in materials science, such as the development of new polymers with tailored properties, or in the creation of novel catalysts for chemical processes.
Used in Research and Development:
(2R,3S)-1-benzyl 4-tert-butyl 3-(cyclopropylmethyl)-2-(3,3,3-5 trifluoropropyl)succinate is also used as a research tool in academic and industrial laboratories. Its structural diversity and potential reactivity make it an interesting subject for studies aimed at understanding new synthetic methods, exploring the biological activity of complex molecules, and investigating the effects of chirality on chemical and biological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1581734-69-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,1,7,3 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1581734-69:
(9*1)+(8*5)+(7*8)+(6*1)+(5*7)+(4*3)+(3*4)+(2*6)+(1*9)=191
191 % 10 = 1
So 1581734-69-1 is a valid CAS Registry Number.
1581734-69-1Relevant articles and documents
A Practical Approach for Enantio- and Diastereocontrol in the Synthesis of 2,3-Disubstituted Succinic Acid Esters: Synthesis of the pan-Notch Inhibitor BMS-906024
Quesnelle, Claude A.,Gill, Patrice,Kim, Soong-Hoon,Chen, Libing,Zhao, Yufen,Fink, Brian E.,Saulnier, Mark,Frennesson, David,DeMartino, Michael P.,Baran, Phil S.,Gavai, Ashvinikumar V.
, p. 2254 - 2258 (2016/10/19)
An oxidative intermolecular enolate heterocoupling reaction was employed for the synthesis of anti-2,3-disubstituted succinic acid mono- and differentially protected diesters. Tactical approaches to access all the diastereomers are discussed. The method w
ALKYL, FLUOROALKYL-1,4-BENZODIAZEPINONE COMPOUNDS
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Paragraph 00257, (2014/04/04)
Disclosed are compounds of Formula (I) and/or salts thereof: (I) wherein: R1 is CH2CH2CF3; R2 is CH2(cyclopropyl), CH(CH3)(cyclopropyl), or CH2CH2CH3/
