Phenyl Methanesulfonate

≥98%

Reagent Code: #122952
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CAS Number 16156-59-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.2 g/mol
Formula C₇H₈O₃S
badge Registry Numbers
MDL Number MFCD00095143
thermostat Physical Properties
Melting Point 59-63°C
Boiling Point 279°C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Phenyl methanesulfonate is primarily used as an alkylating agent in organic synthesis, where it introduces the phenyl group into various molecules. It is particularly valuable in the pharmaceutical industry for the modification of active pharmaceutical ingredients (APIs) to enhance their efficacy or stability. Additionally, it serves as a reagent in the preparation of intermediates for dyes, agrochemicals, and other fine chemicals. Its role in cross-coupling reactions also makes it useful in the development of complex organic compounds. In research, it is employed to study reaction mechanisms involving sulfonate esters.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White To Almost White To Light Brown Powder To Crystal
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿450.00
inventory 100g
10-20 days ฿18,150.00
inventory 25g
10-20 days ฿4,590.00
inventory 5g
10-20 days ฿980.00
Phenyl Methanesulfonate
Phenyl methanesulfonate is primarily used as an alkylating agent in organic synthesis, where it introduces the phenyl group into various molecules. It is particularly valuable in the pharmaceutical industry for the modification of active pharmaceutical ingredients (APIs) to enhance their efficacy or stability. Additionally, it serves as a reagent in the preparation of intermediates for dyes, agrochemicals, and other fine chemicals. Its role in cross-coupling reactions also makes it useful in the development of complex organic compounds. In research, it is employed to study reaction mechanisms involving sulfonate esters.
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