19853-18-0 Usage
Uses
Used in Pharmaceutical Industry:
(Biphenyl-2-ylmethyl)propanedioic acid is used as an intermediate in the synthesis of various pharmaceuticals due to its unique chemical structure and reactivity. It can be incorporated into the development of new drugs, potentially contributing to the treatment of various medical conditions.
Used in Fragrance Industry:
In the fragrance industry, (biphenyl-2-ylmethyl)propanedioic acid is used as a building block for creating complex and unique scents. Its chemical properties allow for the formation of a wide range of fragrant compounds, enhancing the diversity of fragrances available on the market.
Used in Polymer Additives:
(Biphenyl-2-ylmethyl)propanedioic acid is also utilized in the production of polymer additives. These additives can improve the performance characteristics of polymers, such as their stability, durability, and resistance to various environmental factors.
Used in Organic Synthesis:
As a building block in organic synthesis, (biphenyl-2-ylmethyl)propanedioic acid enables the creation of a broad spectrum of organic compounds with different applications, from specialty chemicals to advanced materials.
Used as a Ligand in Metal Ion Coordination:
(Biphenyl-2-ylmethyl)propanedioic acid can act as a ligand for metal ion coordination, which is essential in various chemical and biological processes. Its ability to form stable complexes with metal ions can be exploited in the development of catalysts, sensors, and other applications where metal ion coordination plays a crucial role.
Check Digit Verification of cas no
The CAS Registry Mumber 19853-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,5 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19853-18:
(7*1)+(6*9)+(5*8)+(4*5)+(3*3)+(2*1)+(1*8)=140
140 % 10 = 0
So 19853-18-0 is a valid CAS Registry Number.
19853-18-0Relevant academic research and scientific papers
4-Phenyl-2-indanyl esters of 1R,cis-3-(2-halo-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylic acid
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, (2008/06/13)
Insecticidal 4-phenyl-2-indanyl 1R,cis-3-(2-halo-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarboxylates having a racemic or optically active indanyl moiety, methods of preparation and use, and efficacy data against representative insect species are disclosed and exemplified.
Insecticidal pyrethroid enantiomer pair
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, (2008/06/13)
An insecticidal enantiomer pair consisting essentially of a substantially equimolar mixture of S-4-phenyl-2-indanyl 1R, cis-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarboxylate and R-4-phenyl-2-indanyl 1S,cis-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarboxylate, its preparation by liquid chromatography, and its utility as an insecticide are described and exemplified.
4-Substituted-2-indanols
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, (2008/06/13)
Novel compounds of the formula STR1 are disclosed in which R1 is a phenyl, phenoxy, phenylthio, benzyl or heterocyclic radical which may be substituted, and R2 is hydrogen. The compounds are intermediates of cyclopropanecarboxylate and related insecticides.
4-Substituted-2-indanol insecticidal ester derivatives
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, (2008/06/13)
Novel compounds of the formula STR1 are disclosed in which R1 is a phenyl, phenoxy, phenylthio, benzyl or heterocyclic radical which may be substituted, and R2 is hydrogen, a substituted-vinylcyclopropanecarbonyl group, a tetramethylcyclopropanecarbonyl group, or a 1-(substituted-phenyl)-2-methylpropylcarbonyl group. The compounds wherein R2 is other than hydrogen are insecticides.
