1044169-05-2 Usage
Uses
Used in Organic Synthesis:
(1R,2R,4R)-2-BROMO-1-ISOPROPYL-4-METHYLCYCLOHEXANE is used as a building block in organic synthesis for the creation of complex molecules with specific biological or chemical properties. Its unique structure and stereochemistry make it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Drug Development:
In the pharmaceutical industry, (1R,2R,4R)-2-BROMO-1-ISOPROPYL-4-METHYLCYCLOHEXANE is utilized as a key intermediate in the development of new drugs. Its reactivity, due to the bromine atom and the isopropyl and methyl groups, allows for further derivatization, enabling the generation of a diverse array of compounds with different properties and therapeutic applications.
Used in Chemical Research:
(1R,2R,4R)-2-BROMO-1-ISOPROPYL-4-METHYLCYCLOHEXANE is also employed in chemical research as a model compound to study the effects of stereochemistry on molecular properties and reactivity. Its chiral nature provides insights into the behavior of enantiomers and their interactions with other molecules, which is crucial for understanding the selectivity of chemical reactions and the development of enantioselective synthesis methods.
Check Digit Verification of cas no
The CAS Registry Mumber 1044169-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,4,1,6 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1044169-05:
(9*1)+(8*0)+(7*4)+(6*4)+(5*1)+(4*6)+(3*9)+(2*0)+(1*5)=122
122 % 10 = 2
So 1044169-05-2 is a valid CAS Registry Number.
1044169-05-2Relevant academic research and scientific papers
Synthesis and reactions of enantiomerically pure dialkyl diselenides from the p-menthane group
Rafinski, Zbigniew,Scianowski, Jacek
, p. 1237 - 1244 (2008/09/21)
A convenient route for the synthesis of optically active dialkyl diselenides from the p-menthane system utilizing a reaction of alkyl tosylates and chlorides with sodium diselenide is reported. The diselenides obtained have been used for asymmetric methoxyselenenylation of styrene. Quantum chemical calculations of the chair conformers stability of the terpeneselenenyl bromides from the p-menthane group have also been carried out using density functional theory (DFT, at the B3LYP/6-311G(d) level). The influence of the diselenides structure on the stereoselectivity in the methoxyselenenylation reaction is also discussed.
