1-tert-butyl-4-methanesulfonylbenzene

≥95%

Reagent Code: #238598
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CAS Number 22796-14-1

science Other reagents with same CAS 22796-14-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.3085 g/mol
Formula C₁₁H₁₆O₂S
badge Registry Numbers
MDL Number MFCD15527513
thermostat Physical Properties
Melting Point 94-96 °C
Boiling Point 331.1±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.072±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

1-tert-Butyl-4-methanesulfonylbenzene serves as a key intermediate in organic synthesis, especially within pharmaceutical and agrochemical sectors. The methanesulfonyl group (-SO2CH3) functions as an electron-withdrawing moiety that enables deprotonation at the alpha-methyl position, facilitating umpolung reactivity. This compound is particularly valuable in modified Julia olefination reactions (e.g., Julia-Kocienski), where the sulfone acts as a leaving group in the formation of alkenes from aldehydes. The tert-butyl substituent enhances steric protection and influences solubility and stability in target molecules. Additionally, it is used in constructing complex aromatic frameworks for API development and material science applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,600.00
inventory 250mg
10-20 days ฿48,000.00
inventory 1g
10-20 days ฿80,000.00

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1-tert-butyl-4-methanesulfonylbenzene
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1-tert-Butyl-4-methanesulfonylbenzene serves as a key intermediate in organic synthesis, especially within pharmaceutical and agrochemical sectors. The methanesulfonyl group (-SO2CH3) functions as an electron-withdrawing moiety that enables deprotonation at the alpha-methyl position, facilitating umpolung reactivity. This compound is particularly valuable in modified Julia olefination reactions (e.g., Julia-Kocienski), where the sulfone acts as a leaving group in the formation of al

1-tert-Butyl-4-methanesulfonylbenzene serves as a key intermediate in organic synthesis, especially within pharmaceutical and agrochemical sectors. The methanesulfonyl group (-SO2CH3) functions as an electron-withdrawing moiety that enables deprotonation at the alpha-methyl position, facilitating umpolung reactivity. This compound is particularly valuable in modified Julia olefination reactions (e.g., Julia-Kocienski), where the sulfone acts as a leaving group in the formation of alkenes from aldehydes. The tert-butyl substituent enhances steric protection and influences solubility and stability in target molecules. Additionally, it is used in constructing complex aromatic frameworks for API development and material science applications.

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