140176-60-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C), 13 hydrogen (H), 2 fluorine (F), and 2 oxygen (O) atoms.
Explanation
A chiral compound is one that cannot be superimposed on its mirror image. This means it has a non-superimposable mirror image, which is also known as a stereoisomer.
Explanation
Enantiomers are stereoisomers that are mirror images of each other. In this case, the compound exists in two enantiomeric forms, (R)-1-butanol and (S)-1-butanol, which are non-superimposable mirror images of each other.
Explanation
Specific rotation is a measure of the optical activity of a chiral compound, which is its ability to rotate the plane of polarized light. A positive value indicates that the compound rotates the light to the right (dextrorotatory), while a negative value indicates rotation to the left (levorotatory).
Explanation
The compound in question is the (R)-enantiomer, which means it is the form of the chiral compound that rotates the plane of polarized light to the right.
Explanation
The compound is used in organic synthesis, which is the study and construction of carbon-containing compounds. It can be used as a building block or reagent in the formation of more complex molecules.
Explanation
The compound can act as a solvent in various chemical reactions, providing a medium for the reactants to mix and interact, facilitating the reaction process.
Explanation
The compound has potential applications in the pharmaceutical industry, particularly as a chiral building block in the synthesis of pharmaceutical compounds. Chiral compounds are often important in drug development, as they can have different biological activities depending on their stereochemistry.
Explanation
The stereochemistry of a compound refers to the spatial arrangement of its atoms. In this case, the compound has an (R)-configuration, which is a specific type of stereochemistry that can be determined using the Cahn-Ingold-Prelog priority rules.
Chiral Compound
Yes
Enantiomeric Forms
(R)-1-butanol and (S)-1-butanol
Specific Rotation
+13.0°
(R)-enantiomer
Yes
Application in Organic Synthesis
Yes
Solvent in Chemical Reactions
Yes
Potential Pharmaceutical Applications
Yes
Stereochemistry
(R)-configuration
Check Digit Verification of cas no
The CAS Registry Mumber 140176-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,1,7 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 140176-60:
(8*1)+(7*4)+(6*0)+(5*1)+(4*7)+(3*6)+(2*6)+(1*0)=99
99 % 10 = 9
So 140176-60-9 is a valid CAS Registry Number.
140176-60-9Relevant academic research and scientific papers
Asymmetric Synthesis of Oxygen- and Nitrogen-Substituted Difluoromethylene Products
Bravo, Pierfrancesco,Pregnolato, Massimo,Resnati, Giuseppe
, p. 2726 - 2731 (2007/10/02)
1,1-Difluoroalkyl sulfinylmethyl ketones 3 are synthesized in enantiomerically pure form through acylation of (+)-(R)-methyl p-tolyl sulfoxide (1) with α,α-difluorocarboxylates 2.These ketones have been reduced with complete diastereoselection to give the
