649552-56-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
A chiral compound is one that has a non-superimposable mirror image, meaning it cannot be mapped onto its mirror image by any combination of rotations and translations.
Explanation
Due to potential hazardous properties, it is crucial to take necessary precautions when working with 1,3-Dioxane-2-ethanamine,2-ethyl-alpha-pentyl-,(alphaR)-(9CI) to prevent any adverse effects or accidents.
Explanation
The stereochemistry of a compound refers to the spatial arrangement of its atoms. In this case, the compound has a specific configuration at the alpha (α) carbon, which is designated as R according to the Cahn-Ingold-Prelog priority rules.
Explanation
This term describes the arrangement of atoms and functional groups within the molecule, providing a detailed description of its structure.
Explanation
The compound may have hazardous properties, such as toxicity, flammability, or reactivity, which can pose risks to human health or the environment if not handled correctly.
Chiral Compound
Yes
Applications
Reagent in organic synthesis
Intermediate in the production of pharmaceuticals and agrochemicals
Potential use in the development of new materials and chemical processes
Safety Precautions
Handle with care and follow proper safety protocols
Stereochemistry
alphaR
Chemical Structure
1,3-Dioxane-2-ethanamine, 2-ethyl-alpha-pentyl
Hazardous Properties
Potential hazards if not used properly
Check Digit Verification of cas no
The CAS Registry Mumber 649552-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,9,5,5 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 649552-56:
(8*6)+(7*4)+(6*9)+(5*5)+(4*5)+(3*2)+(2*5)+(1*6)=197
197 % 10 = 7
So 649552-56-7 is a valid CAS Registry Number.
649552-56-7Relevant academic research and scientific papers
Direct Asymmetric Synthesis of β-Amino Ketones from Sulfinimines (N-Sulfinylimines). Synthesis of (-)-Indolizidine 209B
Davis, Franklin A.,Yang, Bin
, p. 5011 - 5014 (2007/10/03)
(Equation presented) N-Sulfinyl β-amino ketones, prepared directly from the potassium enolates of methyl ketones and enantiopure sulfinimines, are transformed in one pot to protected amino ketones, which are valuable chiral building blocks for the assembl
