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4-Hydroxy-3-[(phenylmethoxy)acetyl]-2(5H)-furanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145436-98-2

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145436-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145436-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,4,3 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145436-98:
(8*1)+(7*4)+(6*5)+(5*4)+(4*3)+(3*6)+(2*9)+(1*8)=142
142 % 10 = 2
So 145436-98-2 is a valid CAS Registry Number.

145436-98-2Relevant academic research and scientific papers

A synthetic route to α-substituted butenolides: Enantioselective synthesis of (+)-ancepsenolide

Ghobril, Cynthia,Kister, Jeremy,Baati, Rachid

supporting information; experimental part, p. 3416 - 3419 (2011/09/13)

A variety of α-substituted butenolides was efficiently synthesized starting from commercially available tetronic acid and carboxylic acids in four steps. The effectiveness of this approach is illustrated in the short synthesis of one of the first butenoli

TETRONIC AND THIOTETRONIC ACID DERIVATIVES AS PHOSPHOLIPASE A2 INHIBITORS

-

, (2008/06/13)

There are disclosed compounds of the formula: wherein X is ?CH2R; R is and further when Y=S, R may also be ?(CH2)eCH3; Y is ?O?or ?S?; R1 and R2 are each, independently, hydrogen or lower alkyl; R3 is indolyl, furyl, phenyl or phenyl optionally mono- or disubstituted independently by alkyl of 1-7 carbon atoms, ?C(CH3)3, ?C(CH3)2CH2C(CH3), ?C(CH3)2CH2CH3, haloloweralkyl, perfluoroalkyl, lower alkoxy, aryl alkoxy, halo or nitro; R4 and R5 are, independently, ?COCH2R7, ?CO2R7, ?CONHR7, geranyl or CH2R3; R6 is hydrogen or lower alkyl; R7 is geranyl and any moiety selected from R other than AR5 A and B are, independently, ?O?, ?S? or ?NR6 ?; and a is 0-8; b is 1-10 when Y=S, and 2-10 when Y=0; c is 1-3; d is 0-9; and e is 3-18; which by virtue of their ability to inhibit PLA2, are ofuse as antiinflammatory agents and there is also disclosed a method for the treatment of immunoinflammatory conditions, such as allergy, anaphylaxis, asthma and inflammation in mammals

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