1-tert-butyl-4-methanesulfonylbenzene

≥95%

Reagent Code: #238598
fingerprint
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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿25,600.00
250mg
10-20 days ฿48,000.00
1g
10-20 days ฿80,000.00
1-tert-butyl-4-methanesulfonylbenzene
No image available

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.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...