N'-(3,3-Dimethyl-5-oxocyclohexylidene)-4-methylbenzenesulfonohydrazide

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Reagent Code: #219854
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CAS Number 41189-09-7

science Other reagents with same CAS 41189-09-7

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inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds with potential biological activity. This tosylhydrazone derivative is valuable in pharmaceutical and agrochemical research for further transformations, such as the generation of alkenes via the Shapiro reaction or diazo compounds for insertion reactions. Its unique structure, featuring a substituted cyclohexanone hydrazone, supports the development of novel compounds with possible antimicrobial or anti-inflammatory properties. Also applied in coordination chemistry as a ligand for metal ions, aiding in the design of metal-organic frameworks or catalysts.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿880.00
inventory 1g
10-20 days ฿2,360.00
inventory 25g
10-20 days ฿33,060.00
inventory 5g
10-20 days ฿8,910.00

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N'-(3,3-Dimethyl-5-oxocyclohexylidene)-4-methylbenzenesulfonohydrazide
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Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds with potential biological activity. This tosylhydrazone derivative is valuable in pharmaceutical and agrochemical research for further transformations, such as the generation of alkenes via the Shapiro reaction or diazo compounds for insertion reactions. Its unique structure, featuring a substituted cyclohexanone hydrazone, supports the development of novel compounds with possible antimicrobial or anti

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds with potential biological activity. This tosylhydrazone derivative is valuable in pharmaceutical and agrochemical research for further transformations, such as the generation of alkenes via the Shapiro reaction or diazo compounds for insertion reactions. Its unique structure, featuring a substituted cyclohexanone hydrazone, supports the development of novel compounds with possible antimicrobial or anti-inflammatory properties. Also applied in coordination chemistry as a ligand for metal ions, aiding in the design of metal-organic frameworks or catalysts.

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