N,N-Bis(2-chloroethyl)-p-toluenesulfonamide

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Reagent Code: #77612
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CAS Number 42137-88-2

science Other reagents with same CAS 42137-88-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.22 g/mol
Formula C₁₁H₁₅Cl₂NO₂S
badge Registry Numbers
MDL Number MFCD00018944
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Primarily used in organic synthesis, this chemical serves as an intermediate in the production of various pharmaceutical compounds. It plays a crucial role in the development of antitumor agents, particularly in the synthesis of nitrogen mustard derivatives, which are known for their chemotherapeutic properties. Additionally, it is utilized in research settings to study alkylating agents and their mechanisms of action in cancer therapy. Its application extends to the modification of polymers, where it aids in the introduction of functional groups to enhance material properties.

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Test Parameter Specification
Appearance White to Light Yellow Powder or Crystal
Purity 90-100
Proton NMR Spectrum Conforms to Structure
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿3,040.00
inventory 5g
10-20 days ฿980.00
inventory 100g
10-20 days ฿8,700.00

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N,N-Bis(2-chloroethyl)-p-toluenesulfonamide
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Primarily used in organic synthesis, this chemical serves as an intermediate in the production of various pharmaceutical compounds. It plays a crucial role in the development of antitumor agents, particularly in the synthesis of nitrogen mustard derivatives, which are known for their chemotherapeutic properties. Additionally, it is utilized in research settings to study alkylating agents and their mechanisms of action in cancer therapy. Its application extends to the modification of polymers, where it ai

Primarily used in organic synthesis, this chemical serves as an intermediate in the production of various pharmaceutical compounds. It plays a crucial role in the development of antitumor agents, particularly in the synthesis of nitrogen mustard derivatives, which are known for their chemotherapeutic properties. Additionally, it is utilized in research settings to study alkylating agents and their mechanisms of action in cancer therapy. Its application extends to the modification of polymers, where it aids in the introduction of functional groups to enhance material properties.

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