heptadecan-9-yl 4-Methylbenzenesulfonate

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Reagent Code: #202835
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CAS Number 949898-99-1

science Other reagents with same CAS 949898-99-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 410.65 g/mol
Formula C₂₄H₄₂O₃S
badge Registry Numbers
MDL Number MFCD14635845
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of long-chain alkylated aromatic derivatives. Its sulfonate ester group acts as a good leaving group, facilitating nucleophilic substitution reactions. It is employed in the development of surfactants, lubricants, and specialty chemicals where a long hydrophobic chain is required. The tosylate functionality allows for chain extension or functionalization in pharmaceutical and polymer research. Due to its stability and reactivity profile, it is also utilized in alkylation processes and in the synthesis of complex molecules requiring selective transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,800.00
inventory 250mg
10-20 days ฿11,900.00
inventory 1g
10-20 days ฿35,600.00

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heptadecan-9-yl 4-Methylbenzenesulfonate
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of long-chain alkylated aromatic derivatives. Its sulfonate ester group acts as a good leaving group, facilitating nucleophilic substitution reactions. It is employed in the development of surfactants, lubricants, and specialty chemicals where a long hydrophobic chain is required. The tosylate functionality allows for chain extension or functionalization in pharmaceutical and polymer research. Due to its stabi

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of long-chain alkylated aromatic derivatives. Its sulfonate ester group acts as a good leaving group, facilitating nucleophilic substitution reactions. It is employed in the development of surfactants, lubricants, and specialty chemicals where a long hydrophobic chain is required. The tosylate functionality allows for chain extension or functionalization in pharmaceutical and polymer research. Due to its stability and reactivity profile, it is also utilized in alkylation processes and in the synthesis of complex molecules requiring selective transformations.

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