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1821022-18-7

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1821022-18-7 Usage

Description

Benzyl(R)-2-methyl-2-(methylsulfonyl)pent-4-enoate is a versatile chemical compound characterized by the presence of a benzyl group, a methylsulfonyl group, and a pent-4-enoate group. This unique structure endows it with a wide range of applications in various industries, including pharmaceuticals, agrochemicals, and the production of flavors and fragrances.

Uses

Used in Organic Synthesis:
Benzyl(R)-2-methyl-2-(methylsulfonyl)pent-4-enoate is utilized as a key intermediate in organic synthesis, particularly for the production of complex organic molecules. Its benzyl and methylsulfonyl groups contribute to its versatility in the synthesis process.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, benzyl(R)-2-methyl-2-(methylsulfonyl)pent-4-enoate is employed as a building block for the development of various pharmaceuticals. Its unique structure allows for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
Benzyl(R)-2-methyl-2-(methylsulfonyl)pent-4-enoate also finds use in the agrochemical industry, where it serves as a precursor for the synthesis of agrochemicals. Its properties make it suitable for the development of new compounds with potential applications in agriculture.
Used in Flavors and Fragrances Industry:
Due to its unique structure, benzyl(R)-2-methyl-2-(methylsulfonyl)pent-4-enoate is used in the production of flavors and fragrances. Its presence in the compound contributes to the creation of distinct scents and tastes, making it valuable in the development of new products in this industry.
Used in Ester-based Compounds Production:
The pent-4-enoate group in benzyl(R)-2-methyl-2-(methylsulfonyl)pent-4-enoate makes it useful in the production of ester-based compounds for various industrial applications. Its versatility in ester synthesis allows for the development of new compounds with potential uses in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1821022-18-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,2,1,0,2 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1821022-18:
(9*1)+(8*8)+(7*2)+(6*1)+(5*0)+(4*2)+(3*2)+(2*1)+(1*8)=117
117 % 10 = 7
So 1821022-18-7 is a valid CAS Registry Number.

1821022-18-7Downstream Products

1821022-18-7Relevant articles and documents

ISOXAZOLE HYDROXAMIC ACID COMPOUNDS AS LpxC INHIBITORS

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Paragraph 0411-0414, (2016/07/05)

This invention pertains generally to compounds of Formula I as described herein and compositions containing such compounds, as well as methods of using such compounds to treat bacterial infections. In certain aspects, the invention provides methods and co

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