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(S,S)-trans-2-(hydroxymethyl)cyclopropane carboxylic acid is a chemical compound characterized by its molecular formula C6H10O3. It features a cyclic carboxylic acid structure with a hydroxymethyl group attached to a cyclopropane ring. (S,S)-trans-2-(hydroxymethyl)cyclopropane carboxylic acid is distinguished by its stereochemistry, specifically the trans configuration at the cyclopropane ring, which is crucial for certain chemical reactions. As a versatile and valuable chemical building block, (S,S)-trans-2-(hydroxymethyl)cyclopropane carboxylic acid holds potential in various applications across the fields of chemistry and related industries.

83680-85-7

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83680-85-7 Usage

Uses

Used in Organic Synthesis:
(S,S)-trans-2-(hydroxymethyl)cyclopropane carboxylic acid is used as a key intermediate in organic synthesis for the creation of various complex molecules. Its unique structure and reactivity make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S,S)-trans-2-(hydroxymethyl)cyclopropane carboxylic acid is utilized as a building block for the development of new pharmaceuticals. Its specific stereochemistry and functional groups allow for the design and synthesis of novel drug candidates with potential therapeutic applications.
Used in Pharmaceutical Development:
(S,S)-trans-2-(hydroxymethyl)cyclopropane carboxylic acid is employed as a starting material in the development of pharmaceuticals. Its unique structural features and the ability to undergo various chemical transformations make it an attractive candidate for the creation of new drugs with improved efficacy and selectivity.
Used in Agrochemical Development:
Similarly, in the agrochemical industry, (S,S)-trans-2-(hydroxymethyl)cyclopropane carboxylic acid is used as a chemical building block for the synthesis of new agrochemicals. Its potential applications include the development of novel pesticides, herbicides, and other agricultural chemicals that can enhance crop protection and yield.
Overall, (S,S)-trans-2-(hydroxymethyl)cyclopropane carboxylic acid is a versatile compound with a wide range of applications in organic synthesis, medicinal chemistry, pharmaceutical development, and agrochemical development. Its unique structural features and stereochemistry make it an important player in the design and synthesis of new molecules with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 83680-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,8 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83680-85:
(7*8)+(6*3)+(5*6)+(4*8)+(3*0)+(2*8)+(1*5)=157
157 % 10 = 7
So 83680-85-7 is a valid CAS Registry Number.

83680-85-7Relevant academic research and scientific papers

Enzymes in Organic Synthesis. 24. Preparations of Enantiomerically Pure Chiral Lactones via Stereospecific Horse Liver Alcohol Dehydrogenase Catalyzed Oxidations of Monocyclic Meso Diols

Jakovac, Ignac J.,Goodbrand, H. Bruce,Lok, Kar P.,Jones, J. Bryan

, p. 4659 - 4665 (1982)

Preparative-scale horse liver alcohol dehydrogenase catalyzed oxidation of monocyclic meso diols provides a direct and convenient one-step route to a broad range of chiral γ-lactones of value as synthons in asymmetric synthesis.The general applicability of the method is demonstrated by oxidations of cis-1,2-bis(hydroxymethyl) substrates of the cyclohexyl, cyclohexenyl, cyclopentyl, cyclobutyl, cyclopropyl, and dimethylcyclopropyl series.For each diol, oxidation of the hydroxymethyl group attached to the S chiral center occurs exclusively, and the pure γ-lactone products are isolated in high (68-90percent) yields and of 100percent ee.In contrast, the enzyme does not exhibit significant enantiomeric selectivity in its catalysis of oxidations of the corresponding racemic trans diols.The stereospecificities observed, or lack thereof, are as predicted by the active-site model.

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