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(2-benzyl-6-oxa-2-azaspiro[4.5]decan-9-yl) methanesulfonate is a chemical compound with the molecular formula C16H23NO4S. It is a derivative of spiro compounds, which are a class of organic compounds containing a spiro (or "bridged") ring system. This specific compound features a benzyl group, an oxa group, an azaspiro group, and a methanesulfonate group. It has potential applications in various fields, including pharmaceuticals, agricultural chemicals, and materials science. Additionally, it may exhibit biological activity, making it a subject of interest for researchers and drug developers for potential medicinal uses.

503551-93-7

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503551-93-7 Usage

Uses

Used in Pharmaceutical Industry:
(2-benzyl-6-oxa-2-azaspiro[4.5]decan-9-yl) methanesulfonate is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and functional groups make it a valuable building block in the development of new drugs with potential therapeutic applications.
Used in Agricultural Chemicals:
In the agricultural sector, (2-benzyl-6-oxa-2-azaspiro[4.5]decan-9-yl) methanesulfonate is used as a precursor in the production of agrochemicals. Its properties may contribute to the development of new pesticides, herbicides, or other agricultural products that can improve crop yield and protect plants from pests and diseases.
Used in Materials Science:
(2-benzyl-6-oxa-2-azaspiro[4.5]decan-9-yl) methanesulfonate is utilized in materials science for the development of novel materials with specific properties. Its incorporation into polymers, coatings, or other materials can lead to the creation of innovative products with improved characteristics, such as enhanced stability, durability, or specific interactions with other molecules.
Used in Research and Development:
Due to its potential biological activity, (2-benzyl-6-oxa-2-azaspiro[4.5]decan-9-yl) methanesulfonate is used in research and development for exploring its interactions with biological systems. This can lead to the discovery of new therapeutic targets, drug candidates, or other applications in the life sciences.

Check Digit Verification of cas no

The CAS Registry Mumber 503551-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,5,5 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 503551-93:
(8*5)+(7*0)+(6*3)+(5*5)+(4*5)+(3*1)+(2*9)+(1*3)=127
127 % 10 = 7
So 503551-93-7 is a valid CAS Registry Number.

503551-93-7Downstream Products

503551-93-7Relevant academic research and scientific papers

Multicomponent reactions: Synthesis of spirocyclic tetrahydropyran derivatives by prins cyclization

Ghosh, Arun K.,Shin, Dongwoo,Schiltz, Gary

, p. 659 - 666 (2007/10/03)

Substituted spirocyclic tetrahydropyranyl mesylates and tosylates have been synthesized in good yields using a Prins-type cyclization of various cyclic ketones, a homoallylic alcohol and either methanesulfonic or p-toluenesulfonic acid under non-aqueous conditions. The mesylates thus produced could then be transformed into the corresponding Boc-protected amines using an efficient two step procedure.

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