749885-70-9 Usage
Molecular structure
2-[(1S,2S)-2-tert-butylcyclopropyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane consists of a unique cyclopropyl ring with a tert-butyl substituent and multiple methyl groups attached to a boron atom within a dioxaborolane ring.
Type of compound
It is a complex organic compound containing a boron atom.
Stereochemistry
The compound has (1S,2S) stereochemistry, indicating the specific spatial arrangement of the tert-butylcyclopropyl group.
Functional groups
The compound contains a cyclopropyl ring, a dioxaborolane ring, and multiple methyl groups.
Applications
It is used in various applications, including organic synthesis and as a reagent in chemical reactions.
Specific properties
The compound's unique structure and properties make it useful in a range of chemical processes and research endeavors.
Potential applications
2-[(1S,2S)-2-tert-butylcyclopropyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is of interest for its potential biological and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 749885-70-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,9,8,8 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 749885-70:
(8*7)+(7*4)+(6*9)+(5*8)+(4*8)+(3*5)+(2*7)+(1*0)=239
239 % 10 = 9
So 749885-70-9 is a valid CAS Registry Number.
749885-70-9Relevant academic research and scientific papers
Kinetic Enzymatic Resolution of Cyclopropane Derivatives
Pietruszka, Joerg,Rieche, Anja C. M.,Wilhelm, Thorsten,Witt, Andreas
, p. 1273 - 1286 (2007/10/03)
The kinetic enzymatic resolution of various cyclopropane derivatives was systematically investigated. The study focused on synthetically useful cyclopropylmethanols (e.g., 18a/j or 19a/j) as well as some rarely investigated cyclopropanols (e.g., 24/25 or 27). The combination of enantioselective catalytic or diastereoselective synthesis of enantiomerically enriched compounds with enzymatic approaches ultimately led to the most convenient route to enantiomerically pure starting materials. Again, this was especially proven for the synthesis of cyclopropanols 18a/j and 19a/j. Key to the successful investigation was to rigorously establish an analytical tool for the analysis of enantiomeric composition of reaction mixtures.
