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5-(phenoxymethyl)-1,3-oxathiolan-2-one is a chemical compound with the molecular formula C10H10O3S. It is a heterocyclic organic molecule that features a 1,3-oxathiolan-2-one ring, which is a five-membered ring containing one oxygen and one sulfur atom. The phenoxymethyl group is attached to the 5-position of the oxathiolan ring, providing a phenyl ring connected to a methoxy group. 5-(phenoxymethyl)-1,3-oxathiolan-2-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a precursor in the production of certain pesticides. Its chemical structure allows for a range of functional group modifications, making it a versatile building block in organic synthesis.

2289-92-1

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2289-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2289-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2289-92:
(6*2)+(5*2)+(4*8)+(3*9)+(2*9)+(1*2)=101
101 % 10 = 1
So 2289-92-1 is a valid CAS Registry Number.

2289-92-1Downstream Products

2289-92-1Relevant academic research and scientific papers

A facile method for the synthesis of 1,3-oxathiolan-2-ones by reaction of oxiranes, sulfur, and carbon monoxide

Nishiyama, Yutaka,Katahira, Chisato,Sonoda, Noboru

, p. 5803 - 5807 (2006)

A new method for the synthesis of 1,3-oxathiolan-2-ones has been developed. When oxiranes were allowed to react with sulfur in the presence of a catalytic amount of sodium hydride under pressurized carbon monoxide, the three-component coupling of oxiranes

A new method for the synthesis of 1,3-oxathiolan-2-ones by the reaction of epoxides with sulfur and carbon monoxide

Nishiyama, Yutaka,Katahira, Chisato,Sonoda, Noboru

, p. 8539 - 8540 (2004)

The convenient method for the synthesis of 1,3-oxathiolan-2-ones by the reaction of epoxides with elemental sulfur and carbon monoxide in the presence of catalytic amount of sodium hydride has been developed.

Synthesis of cyclic monothiocarbonates via the coupling reaction of carbonyl sulfide (COS) with epoxides

Luo,Zhang,Darensbourg

, p. 188 - 192 (2016)

Two guanidine bases were used as organocatalysts for the synthesis of cyclic monothiocarbonates via the coupling reaction of carbonyl sulfide (COS) and epoxides. The systems proved to be efficient single-component, metal-free catalysts for the reaction of

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