7166-45-2 Usage
Chemical structure
1,3-Dioxolane, 2-(chloromethyl)-4,5-dimethyl-
It is a chloromethylated derivative of dioxolane, which means it has a chloromethyl group (CH2Cl) attached to the 2nd carbon of the dioxolane ring, and two methyl groups (CH3) attached to the 4th and 5th carbons.
Physical state
Colorless liquid
The compound is in a liquid state at room temperature and is colorless in appearance.
Odor
Slightly sweet
It has a mild, sweet smell, which can be detected at low concentrations.
Flammability
Flammable
The compound is flammable, meaning it can easily catch fire when exposed to a source of ignition.
Hazardous nature
Potentially hazardous if not handled with care
Due to its flammable and irritating properties, it is important to handle 1,3-Dioxolane, 2-(chloromethyl)-4,5-dimethyl- with care and follow safety protocols.
Safety concerns
Can cause irritation to skin, eyes, and respiratory system
Exposure to the compound can lead to irritation of the skin, eyes, and respiratory system, so proper protective measures should be taken.
Applications
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals
The compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals, making it an important industrial chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 7166-45-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,6 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7166-45:
(6*7)+(5*1)+(4*6)+(3*6)+(2*4)+(1*5)=102
102 % 10 = 2
So 7166-45-2 is a valid CAS Registry Number.
7166-45-2Relevant academic research and scientific papers
Process for producing 2-halomethyl-1,3-cyclic acetal
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, (2008/06/13)
The yield and purity of 2-halomethyl-1,3-cyclic acetals is improved by subjecting the reaction product of 1,2-dihaloethyl acetate and aliphatic diol to alkaline hydrolysis. The resulting aqueous and organic phases are separated and the organic phase distilled to recover the 2-halomethyl-1,3-cyclic acetal product.
