228546-52-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound consists of 11 carbon (C) atoms, 15 hydrogen (H) atoms, 1 nitrogen (N) atom, and 2 oxygen (O) atoms.
Explanation
The compound is derived from a butanol molecule, which is a four-carbon alcohol. A 3-pyridinyloxy group, which contains a nitrogen atom in a pyridine ring, is attached to the fourth carbon atom of the butanol molecule.
Explanation
The compound exists in a liquid state at room temperature and is colorless, meaning it does not have any visible color.
Explanation
The compound has a mild, sweet smell, which is a characteristic of many alcohols and their derivatives.
Explanation
Due to its chemical properties, 1-Butanol,4-(3-pyridinyloxy)-(9CI) is used as a solvent in different industrial processes, helping to dissolve other substances and facilitate chemical reactions.
Explanation
The compound is utilized in the synthesis and formulation of various pharmaceutical products, likely due to its ability to act as a solvent and its compatibility with other chemical components.
Explanation
1-Butanol,4-(3-pyridinyloxy)-(9CI) is employed as a reagent in organic synthesis, which involves the formation of new chemical compounds through the manipulation of carbon-containing molecules.
Explanation
The compound is considered to have low toxicity, meaning it is less harmful to living organisms when compared to other chemicals. However, it is still essential to handle and store the compound properly to minimize any potential risks.
Explanation
When the compound is managed and stored according to safety guidelines, it is deemed safe for use in various applications. Proper handling includes using appropriate personal protective equipment (PPE) and following safety protocols to minimize exposure and potential hazards.
Structure
Butanol molecule with a 3-pyridinyloxy group attached to the fourth carbon atom
Physical State
Colorless liquid
Odor
Mild, sweet
Applications
Solvent in various industrial applications
Pharmaceutical Preparation
Used in the preparation of pharmaceuticals
Organic Synthesis
Reagent in organic synthesis
Toxicity
Low toxicity
Safety
Generally considered safe for use when handled and stored properly
Check Digit Verification of cas no
The CAS Registry Mumber 228546-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,5,4 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 228546-52:
(8*2)+(7*2)+(6*8)+(5*5)+(4*4)+(3*6)+(2*5)+(1*2)=149
149 % 10 = 9
So 228546-52-9 is a valid CAS Registry Number.
228546-52-9Relevant academic research and scientific papers
Bach, Andrew T.,Carlson, John A.,Giannousis, Peter P.
, p. 769 - 774 (1999)
A convergent synthesis of CGS23305 was discovered. The route to the pyridine aldehyde intermediate 5 was reduced from four to two steps. The pyridine aldehyde was converted to the key pyridine aldehyde ester intermediate 7 via Michael Addition of the N,N-diethylenamine 6 to ethyl acrylate. A Wittig alkenation using the multifunctional moiety 19 completed the carbon skeleton assembly. Hydrogenation and hydrolysis afforded CGS23305 in 44% overall yield from 14 (6 steps).
