131484-61-2 Usage
Description
(1S)-2-methyl-3-(2E)-3-[(2R)-oxiran-2-yl]prop-2-en-1-yl-4-oxocyclopent-2-en-1-yl (1R,3R)-3-[(1Z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate is a complex organic molecule with a cyclopentenone ring, a cyclopropanecarboxylate group, and an oxiran-2-yl group, as well as a methoxy and oxopropenyl moiety. It exhibits a high degree of structural complexity and potential for diverse chemical reactivity.
Uses
Used in Pharmaceutical Industry:
(1S)-2-methyl-3-(2E)-3-[(2R)-oxiran-2-yl]prop-2-en-1-yl-4-oxocyclopent-2-en-1-yl (1R,3R)-3-[(1Z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate is used as a pharmaceutical candidate for its potential therapeutic applications due to its complex structure and diverse chemical reactivity.
Used in Materials Science:
(1S)-2-methyl-3-(2E)-3-[(2R)-oxiran-2-yl]prop-2-en-1-yl-4-oxocyclopent-2-en-1-yl (1R,3R)-3-[(1Z)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate is used in materials science for the development of new materials with unique properties, leveraging its structural complexity and chemical reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 131484-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,4,8 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131484-61:
(8*1)+(7*3)+(6*1)+(5*4)+(4*8)+(3*4)+(2*6)+(1*1)=112
112 % 10 = 2
So 131484-61-2 is a valid CAS Registry Number.
131484-61-2Relevant articles and documents
Molecular Markers for Pyrethrin Autoxidation in Stored Pyrethrum Crop: Analysis and Structure Determination
Freemont, Jamie A.,Littler, Stuart W.,Hutt, Oliver E.,Mauger, Stephanie,Meyer, Adam G.,Winkler, David A.,Kerr, Maurice G.,Ryan, John H.,Cole, Helen F.,Duggan, Peter J.
, p. 7134 - 7141 (2016/10/07)
Pyrethrum is a natural insecticide extracted from Tanacetum cinerariifolium. Six esters, the pyrethrins, are responsible for the extract's insecticidal activity. The oxidative degradation of pyrethrins through contact with aerial oxygen is a potential cause of pyrethrin losses during pyrethrum manufacture. Described here is the first investigation of the autoxidation chemistry of the six pyrethrin esters isolated from pyrethrum. It was found that pyrethrins I and II, the major pyrethrin esters present in pyrethrum, undergo autoxidation more readily than the minor pyrethrin esters, the jasmolins and cinerins. Chromatographic analysis of pyrethrin I and II autoxidation mixtures showed some correlation with a similar analysis performed on extracts from T. cinerariifolium crop, which had been stored for 12 weeks without added antioxidants. Two pyrethrin II autoxidation products were isolated, characterized, and shown to be present in extracts of stored T. cinerariifolium crop, confirming that autoxidation of pyrethrin esters does occur during crop storage.
