4-(Vinylsulfonyl)benzoic acid

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Reagent Code: #245379
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CAS Number 95535-40-3

science Other reagents with same CAS 95535-40-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.22 g/mol
Formula C₉H₈O₄S
badge Registry Numbers
MDL Number MFCD11519203
thermostat Physical Properties
Boiling Point 438.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a reactive intermediate in organic synthesis, particularly in the preparation of dyes and pigments due to its ability to form covalent bonds with nucleophiles like amines and thiols. Its vinyl sulfone group enables Michael addition reactions, making it valuable in the development of functional polymers and crosslinking agents. Also employed in biochemical applications for modifying proteins and peptides, where it acts as a labeling or immobilization reagent. Additionally, it serves as a building block in the synthesis of pharmaceuticals and agrochemicals requiring aromatic sulfone scaffolds.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿5,900.00

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4-(Vinylsulfonyl)benzoic acid
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Used as a reactive intermediate in organic synthesis, particularly in the preparation of dyes and pigments due to its ability to form covalent bonds with nucleophiles like amines and thiols. Its vinyl sulfone group enables Michael addition reactions, making it valuable in the development of functional polymers and crosslinking agents. Also employed in biochemical applications for modifying proteins and peptides, where it acts as a labeling or immobilization reagent. Additionally, it serves as a building

Used as a reactive intermediate in organic synthesis, particularly in the preparation of dyes and pigments due to its ability to form covalent bonds with nucleophiles like amines and thiols. Its vinyl sulfone group enables Michael addition reactions, making it valuable in the development of functional polymers and crosslinking agents. Also employed in biochemical applications for modifying proteins and peptides, where it acts as a labeling or immobilization reagent. Additionally, it serves as a building block in the synthesis of pharmaceuticals and agrochemicals requiring aromatic sulfone scaffolds.

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