111003-36-2 Usage
General Description
((2R,3S)-3-propyloxiran-2-yl)methanol is a chemical compound with the molecular formula C6H12O2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and its systematic name is (2R,3S)-3-propyloxiran-2-yl)methanol. ((2R,3S)-3-propyloxiran-2-yl)methanol is also known as (R)-(+)-propylene oxide and is commonly used in the production of polyurethanes, solvents, and other chemicals. It is a colorless, flammable liquid with a slightly sweet odor, and it is considered to be a hazardous substance, with potential health effects including skin and eye irritation, as well as respiratory and central nervous system effects. Therefore, it should be handled and used with caution.
Check Digit Verification of cas no
The CAS Registry Mumber 111003-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,0 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 111003-36:
(8*1)+(7*1)+(6*1)+(5*0)+(4*0)+(3*3)+(2*3)+(1*6)=42
42 % 10 = 2
So 111003-36-2 is a valid CAS Registry Number.
111003-36-2Relevant articles and documents
Process for cooxidizing organic compounds, process for producing epoxy compounds and process for producing esters or lactones
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, (2008/06/13)
According to the inventive co-oxidation process of organic compounds, (A) a compound selected from (A1) a compound having a non-aromatic ethylenic bond and (A2) a ketone or an alcohol corresponding to the ketone is oxidized by molecular oxygen in the presence of N-hydroxyphthalimide or another imide compound and in the coexistence of (B) a compound oxidizable by the imide compound and oxygen and different from the compound (A). As the compound (B), (a) primary or secondary alcohols (e.g., benzhydrol, cyclohexanol), (b) compounds each having a carbon-hydrogen bond at the adjacent position to an unsaturated bond (e.g., tetralin, ethylbenzene) and the like can be used. According to this process, a corresponding epoxy compound from the compound (A1) having a non-aromatic ethylenic bond, and a corresponding ester or lactone from the ketone or its corresponding alcohol (A2) can be obtained in satisfactory yields.