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(1S,4R)-4-acetoxy-5,5-dimethyl-2-cyclopentene-1-ol is a cyclopentene derivative featuring a unique structure with a hydroxyl group at the first carbon and an acetoxy group at the fourth carbon. It also has two methyl groups attached to the cyclopentene ring, contributing to its distinct properties. This chemical is valuable in organic synthesis and serves as a building block for creating other compounds. Its potential biological activity and stereochemistry, with stereocenters at the first and fourth carbons, make it a promising candidate for the development of new pharmaceuticals, agrochemicals, and chiral molecules.

167965-98-2

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167965-98-2 Usage

Uses

Used in Organic Synthesis:
(1S,4R)-4-acetoxy-5,5-dimethyl-2-cyclopentene-1-ol is used as a key intermediate in organic synthesis for the preparation of various complex organic compounds. Its unique structure allows for versatile chemical reactions, facilitating the synthesis of a wide range of molecules.
Used in Pharmaceutical Development:
As a compound with potential biological activity, (1S,4R)-4-acetoxy-5,5-dimethyl-2-cyclopentene-1-ol is used as a starting material in the development of new pharmaceuticals. Its ability to interact with biological targets and its unique stereochemistry make it a valuable asset in the creation of novel drugs.
Used in Agrochemical Development:
(1S,4R)-4-acetoxy-5,5-dimethyl-2-cyclopentene-1-ol is also utilized in the development of new agrochemicals, such as pesticides and herbicides. Its potential to exhibit biological activity against pests and weeds, along with its unique structural features, make it a promising candidate for the design of effective and environmentally friendly agrochemicals.
Used in Chiral Molecule Synthesis:
Due to its stereochemistry with stereocenters at the first and fourth carbons, (1S,4R)-4-acetoxy-5,5-dimethyl-2-cyclopentene-1-ol is used as a precursor in the synthesis of chiral molecules. Chiral molecules have applications in various fields, including pharmaceuticals, where they can exhibit different biological activities and selectivity compared to their non-chiral counterparts.

Check Digit Verification of cas no

The CAS Registry Mumber 167965-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,9,6 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 167965-98:
(8*1)+(7*6)+(6*7)+(5*9)+(4*6)+(3*5)+(2*9)+(1*8)=202
202 % 10 = 2
So 167965-98-2 is a valid CAS Registry Number.

167965-98-2Upstream product

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