4-(Piperidin-1-ylsulfonyl)benzoyl chloride

95%

Reagent Code: #227576
fingerprint
CAS Number 29171-75-3

science Other reagents with same CAS 29171-75-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.76 g/mol
Formula C₁₂H₁₄ClNO₃S
badge Registry Numbers
MDL Number MFCD06496324
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. The benzoyl chloride functionality reacts readily with nucleophiles such as amines and alcohols to form amide or ester derivatives, while the pre-existing piperidin-1-ylsulfonyl (sulfonamide) group contributes to the pharmacophore. This structure is valuable for constructing bioactive molecules, particularly in the development of medicinal compounds incorporating sulfonamide and amide motifs. Its high reactivity enables efficient derivatization in multi-step syntheses, such as creating enzyme inhibitors or receptor ligands. Handle with care due to moisture sensitivity and potential for irritation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,430.00
inventory 250mg
10-20 days ฿8,140.00
inventory 1g
10-20 days ฿22,040.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-(Piperidin-1-ylsulfonyl)benzoyl chloride
No image available

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. The benzoyl chloride functionality reacts readily with nucleophiles such as amines and alcohols to form amide or ester derivatives, while the pre-existing piperidin-1-ylsulfonyl (sulfonamide) group contributes to the pharmacophore. This structure is valuable for constructing bioactive molecules, particularly in the development of medicinal compounds incorporating sulfonamide and amide motifs. Its high react

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. The benzoyl chloride functionality reacts readily with nucleophiles such as amines and alcohols to form amide or ester derivatives, while the pre-existing piperidin-1-ylsulfonyl (sulfonamide) group contributes to the pharmacophore. This structure is valuable for constructing bioactive molecules, particularly in the development of medicinal compounds incorporating sulfonamide and amide motifs. Its high reactivity enables efficient derivatization in multi-step syntheses, such as creating enzyme inhibitors or receptor ligands. Handle with care due to moisture sensitivity and potential for irritation.

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...