406956-07-8 Usage
Chemical Structure
1,3-Dioxan-4-ol, 5,5-dimethyl-2-(1-methylethyl)-(2R,4S)-rel-(9CI)
It is a cyclic ether with a six-membered ring containing two oxygen atoms, with specific substituents at the 1, 3, 4, and 5 positions.
Physical State
Colorless liquid
The compound appears as a colorless liquid at room temperature.
Solubility
Soluble in water
It can dissolve in water, making it suitable for various chemical reactions and applications.
Odor
Mild, sweet
The compound has a pleasant, mild, and sweet smell.
Applications
Synthesis of pharmaceuticals and organic compounds
It is used as a building block or intermediate in the synthesis of various pharmaceuticals and organic compounds.
Additional Applications
Potential use in fragrances and flavors
Due to its pleasant odor, it may have applications in the manufacturing of fragrances and flavors.
Safety Precautions
Causes irritation to skin, eyes, and respiratory system
It is important to handle this compound with care to avoid irritation and potential health risks.
Storage and Usage
Store and use in a well-ventilated area
To minimize the risk of exposure and ensure safety, the compound should be stored and used in a well-ventilated area.
Check Digit Verification of cas no
The CAS Registry Mumber 406956-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,9,5 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 406956-07:
(8*4)+(7*0)+(6*6)+(5*9)+(4*5)+(3*6)+(2*0)+(1*7)=158
158 % 10 = 8
So 406956-07-8 is a valid CAS Registry Number.
406956-07-8Relevant articles and documents
Selective mixed Tishchenko reaction via substituted 1,3-dioxan-4-ols
Toermaekangas, Olli P.,Saarenketo, Pauli,Koskinen, Ari M. P.
, p. 125 - 131 (2013/09/06)
Monoesters of 1,3-diols can be prepared with the mixed Tishchenko reaction from β-hydroxy aldehydes and another aldehyde. These two aldehydes form a diastereomeric mixture of 1,3-dioxan-4-ol hemiacetal derivatives which can be further converted to monoesters with suitable catalysts. Limitations in the formation and esterification of this hemiacetal intermediate have been investigated in this work and the formation and stability of 1,3-dioxan-4-ols was found to be aldehyde-, temperature-, and solvent-dependent. A new method was developed for selective preparation of monoesters of 1,3-diols with this mixed Tishchenko reaction via 1,3-dioxan-4-ols without any significant side products. During the development of this method a possibility to scale up the reactions to reach a selective and economical process was one of the main targets in this work.
