N-Tosylbenzamide

≥95%

Reagent Code: #218160
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CAS Number 6971-74-0

science Other reagents with same CAS 6971-74-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.32 g/mol
Formula C₁₄H₁₃NO₃S
badge Registry Numbers
MDL Number MFCD00431862
inventory_2 Storage & Handling
Density 1.276g/cm3
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the formation of heterocyclic compounds due to the reactivity of the amide and tosyl groups. Commonly employed in the synthesis of sulfonamide-based drugs, where it helps introduce the benzamide moiety in controlled reactions. Also utilized in research settings for peptide modifications and as a protecting group strategy in multi-step syntheses. Its stability and selective deprotection make it valuable in creating complex molecular structures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,330.00
inventory 250mg
10-20 days ฿2,260.00
inventory 1g
10-20 days ฿5,660.00
inventory 5g
10-20 days ฿18,850.00
inventory 25g
10-20 days ฿58,440.00

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N-Tosylbenzamide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the formation of heterocyclic compounds due to the reactivity of the amide and tosyl groups. Commonly employed in the synthesis of sulfonamide-based drugs, where it helps introduce the benzamide moiety in controlled reactions. Also utilized in research settings for peptide modifications and as a protecting group strategy in multi-step syntheses. Its stabili

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the formation of heterocyclic compounds due to the reactivity of the amide and tosyl groups. Commonly employed in the synthesis of sulfonamide-based drugs, where it helps introduce the benzamide moiety in controlled reactions. Also utilized in research settings for peptide modifications and as a protecting group strategy in multi-step syntheses. Its stability and selective deprotection make it valuable in creating complex molecular structures.

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