82010-86-4 Usage
Explanation
The compound is composed of 10 carbon atoms, 22 hydrogen atoms, 4 oxygen atoms, and 2 sulfur atoms.
Explanation
The compound is derived from propanol by replacing a hydrogen atom with a thiol (-SH) group.
Explanation
The compound contains two hydroxyethyl thio groups, which are important functional groups in organic chemistry.
Explanation
Due to its unique structure and properties, the compound is commonly used in the synthesis of various pharmaceuticals and agrochemicals.
Explanation
The compound has a wide range of applications in these fields, thanks to its versatile structure and properties.
Explanation
The compound has a complex molecular structure, which contributes to its diverse applications and properties.
Explanation
Due to the presence of hydroxyl and thiol groups, the compound is likely to be soluble in polar solvents such as water and alcohols.
Explanation
The presence of hydroxyl and thiol groups makes the compound reactive with both electrophilic and nucleophilic reagents, allowing for various chemical reactions and modifications.
Explanation
The compound is generally stable under normal conditions, such as room temperature and pressure, making it suitable for various applications.
Explanation
As with many chemicals, the safety of 1-[(2-hydroxyethyl)thio]-3-[3-[(2-hydroxyethyl)thio]propoxy]propan-2-ol depends on the concentration and the level of exposure. It is essential to follow proper handling and safety protocols when working with 1-[(2-hydroxyethyl)thio]-3-[3-[(2-hydroxyethyl)thio]propoxy]propan-2-ol.
Thiol derivative
Propanol
Functional groups
Two hydroxyethyl thio groups
Applications
Pharmaceutical and agrochemical synthesis
Fields of use
Medicine, agriculture, and industrial chemistry
Molecular structure
Complex organic compound
Solubility
Soluble in polar solvents
Reactivity
Reactive with electrophiles and nucleophiles
Stability
Stable under normal conditions
Safety
Potential hazards depending on concentration and exposure
Check Digit Verification of cas no
The CAS Registry Mumber 82010-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,1 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82010-86:
(7*8)+(6*2)+(5*0)+(4*1)+(3*0)+(2*8)+(1*6)=94
94 % 10 = 4
So 82010-86-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O4S2/c11-2-6-15-5-1-4-14-8-10(13)9-16-7-3-12/h10-13H,1-9H2
82010-86-4Relevant academic research and scientific papers
Method for synthesizing high-purity 1,5,13-trihydroxy-7-oxa-3,11-dithiotridecane and purification method
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Paragraph 0028; 0029; 0030; 0031; 0032; 0033; 0034-0039, (2018/05/16)
The invention discloses a method for synthesizing high-purity 1,5,13-trihydroxy-7-oxa-3,11-dithiotridecane and a purification method. According to the method, mercaptoethanol and allyl glycidyl etherare taken as raw materials and subjected to an addition reaction at the temperature of 60-90 DEG C under the composite catalysis action of tert-butyl peroxybenzoate and tetramethyl guanidine for 7-12h, and a crude product of 1,5,13-trihydroxy-7-oxa-3,11-dithiotridecane is obtained; the crude product is stirred for a reaction at the controlled temperature of 100-160 DEG C under the overbottom pressure of 2.66 kPa in a vacuum state for 2-5 h, low molecular-weight polymers are removed, the purity of the product is increased to 96% or above, and the qualification rate of the product is increasedto 100%. The procedure is simplified, the product quality is improved, the production process is stable to operate, and industrial production is easier to realize.
