131486-45-8 Usage
Description
(1S)-3-[(2R)-2,3-dihydroxypent-4-en-1-yl]-2-methyl-4-oxocyclopent-2-en-1-yl (1R,3R)-3-[(1E)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate is a complex organic molecule that features a cyclopentenone and a cyclopropane carboxylate moiety. It is characterized by the presence of multiple chiral centers, as indicated by the (1S), (2R), (1R), and (3R) stereochemical descriptors, which define the spatial arrangement of substituents around these centers. The molecule also incorporates various functional groups, including hydroxyl, ketone, and methoxy groups. Due to its intricate structure and the diversity of its functional groups, this compound is expected to exhibit unique chemical and biological properties.
Uses
Used in Pharmaceutical Industry:
(1S)-3-[(2R)-2,3-dihydroxypent-4-en-1-yl]-2-methyl-4-oxocyclopent-2-en-1-yl (1R,3R)-3-[(1E)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate is used as a pharmaceutical compound for its potential unique biological activity. The presence of multiple chiral centers and functional groups may contribute to its interaction with biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (1S)-3-[(2R)-2,3-dihydroxypent-4-en-1-yl]-2-methyl-4-oxocyclopent-2-en-1-yl (1R,3R)-3-[(1E)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate serves as a subject of study for understanding the effects of stereochemistry on chemical reactivity and the potential for new synthetic pathways. Its complex structure provides opportunities for exploring novel reactions and mechanisms.
Used in Material Science:
(1S)-3-[(2R)-2,3-dihydroxypent-4-en-1-yl]-2-methyl-4-oxocyclopent-2-en-1-yl (1R,3R)-3-[(1E)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate may be utilized in material science for the development of new materials with specific properties. The molecule's unique structure and functional groups could lead to the creation of materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 131486-45-8 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 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 131486-45:
(8*1)+(7*3)+(6*1)+(5*4)+(4*8)+(3*6)+(2*4)+(1*5)=118
118 % 10 = 8
So 131486-45-8 is a valid CAS Registry Number.
131486-45-8Relevant 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)
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.
