4362-17-8 Usage
Explanation
This is an alternative name for 1,3-Dioxolane, 2-(phenylmethylene)-, which is derived from its structure and the presence of a benzylidene group.
Explanation
The compound is in a liquid state at room temperature and is colorless, meaning it does not have any visible color.
Explanation
The compound has a pleasant and floral scent, which makes it suitable for use in the fragrance industry.
Explanation
The compound has various applications due to its chemical properties, including acting as a solvent, a starting material for the production of pharmaceuticals and fragrances, a reagent in organic synthesis, and a stabilizer in the plastics and polymers industry.
Explanation
The compound is flammable, meaning it can easily catch fire or ignite when exposed to a heat source or flame.
Explanation
Due to its flammability, it is important to handle 1,3-Dioxolane, 2-(phenylmethylene)with care and ensure proper ventilation to minimize the risk of fire or explosion.
Physical State
Colorless liquid
Odor
Pleasant, floral
Uses
Solvent, intermediate in pharmaceuticals and fragrances, reagent in organic synthesis, stabilizer in plastics and polymers
Flammability
Flammable
Safety Precaution
Handle with care in a well-ventilated area
Check Digit Verification of cas no
The CAS Registry Mumber 4362-17-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4362-17:
(6*4)+(5*3)+(4*6)+(3*2)+(2*1)+(1*7)=78
78 % 10 = 8
So 4362-17-8 is a valid CAS Registry Number.
4362-17-8Relevant articles and documents
Structure and thermal reactivity of some 2-substituted 1,3-oxathiolane S-oxides
Aitken, R. Alan,Henderson, Sarah,Slawin, Alexandra M. Z.
, p. 422 - 434 (2018/03/26)
Isomerization of 2-benzylidene-1,3-dioxolane to 3-phenylbutyrolactone occurs readily under flash vacuum pyrolysis (FVP) conditions. 2-Diphenylmethyl-1,3-oxathiolane and 2-benzyl-1,3-oxathiolane have been prepared and the latter compound has been oxidized to the corresponding sulfoxide, whose structure and conformation are examined by 1H NMR, and to the sulfone whose X-ray structure is determined. 2-Benzylidene-1,3-oxathiolane is also prepared and the behavior of the three S-oxidized oxathiolane derivatives upon FVP is examined. While extrusion of SOn to give ethene and a carbonyl compound predominates in all three cases, the sulfoxide gives also bis(2-hydroxyethyl) disulfide, most likely formed via thiirane S-oxide and 1,2-oxathietane.
