5-Bromo-2-thiophenesulfonamide

97%

Reagent Code: #143124
label
Alias 5-Bromothiophene-2-sulfonamide; 5-Bromothiophene-2-sulfonyl chloride, 5-Bromothiophene-sulfonyl chloride
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CAS Number 53595-65-6

science Other reagents with same CAS 53595-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.11 g/mol
Formula C₄H₄BrNO₂S₂
badge Registry Numbers
MDL Number MFCD00067990
thermostat Physical Properties
Melting Point 138-142 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antihypertensive drugs. It serves as a building block in organic synthesis due to the presence of both bromine and sulfonamide functional groups, enabling cross-coupling reactions and derivatization. Its thiophene core contributes to enhanced metabolic stability in drug candidates. Also explored in agrochemical research for designing bioactive molecules with improved selectivity and efficacy.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿350.00
5g
10-20 days ฿750.00
25g
10-20 days ฿2,990.00
100g
10-20 days ฿8,370.00
5-Bromo-2-thiophenesulfonamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antihypertensive drugs. It serves as a building block in organic synthesis due to the presence of both bromine and sulfonamide functional groups, enabling cross-coupling reactions and derivatization. Its thiophene core contributes to enhanced metabolic stability in drug candidates. Also explored in agrochemical research for designing bioactive molecules with improved selectivity and efficacy.<

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antidiabetic and antihypertensive drugs. It serves as a building block in organic synthesis due to the presence of both bromine and sulfonamide functional groups, enabling cross-coupling reactions and derivatization. Its thiophene core contributes to enhanced metabolic stability in drug candidates. Also explored in agrochemical research for designing bioactive molecules with improved selectivity and efficacy.

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