Methyl 3-(chlorosulfonyl)-4-phenyl-5-(trifluoromethyl)thiophene-2-carboxylate

98%

Reagent Code: #214343
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CAS Number 306935-98-8

science Other reagents with same CAS 306935-98-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 384.78 g/mol
Formula C₁₃H₈ClF₃O₄S₂
badge Registry Numbers
MDL Number MFCD02090166
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and antidiabetic compounds. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in sulfonylation reactions to introduce sulfonamide groups, which are prevalent in bioactive molecules. Also utilized in agrochemical research for designing novel pesticides due to its electron-withdrawing trifluoromethyl and chlorosulfonyl groups that enhance stability and reactivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿12,800.00
5g
10-20 days ฿51,970.00
Methyl 3-(chlorosulfonyl)-4-phenyl-5-(trifluoromethyl)thiophene-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and antidiabetic compounds. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in sulfonylation reactions to introduce sulfonamide groups, which are prevalent in bioactive molecules. Also utilized in agrochemical research for designing novel pesticides due to its electron-withdrawing trifluoromethyl

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and antidiabetic compounds. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in sulfonylation reactions to introduce sulfonamide groups, which are prevalent in bioactive molecules. Also utilized in agrochemical research for designing novel pesticides due to its electron-withdrawing trifluoromethyl and chlorosulfonyl groups that enhance stability and reactivity.

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