4-((4-Methylpiperazin-1-yl)methyl)benzoyl chloride hydrochloride

97%

Reagent Code: #46030
fingerprint
CAS Number 909252-77-3

science Other reagents with same CAS 909252-77-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.2008 g/mol
Formula C₁₃H₁₈Cl₂N₂O
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of biologically active molecules. Its reactive benzoyl chloride group makes it a valuable reagent for forming amide bonds, which are crucial in the construction of various drug candidates. It is often employed in the preparation of compounds targeting neurological disorders, as the 4-methylpiperazine moiety can enhance blood-brain barrier penetration. Additionally, it finds application in the production of small molecule inhibitors for enzymes and receptors, contributing to drug discovery efforts in oncology and other therapeutic areas. Its hydrochloride form ensures stability and solubility, making it suitable for use in organic synthesis and medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿369.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-((4-Methylpiperazin-1-yl)methyl)benzoyl chloride hydrochloride
No image available

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of biologically active molecules. Its reactive benzoyl chloride group makes it a valuable reagent for forming amide bonds, which are crucial in the construction of various drug candidates. It is often employed in the preparation of compounds targeting neurological disorders, as the 4-methylpiperazine moiety can enhance blood-brain barrier penetration. Additionally, it finds application in the

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of biologically active molecules. Its reactive benzoyl chloride group makes it a valuable reagent for forming amide bonds, which are crucial in the construction of various drug candidates. It is often employed in the preparation of compounds targeting neurological disorders, as the 4-methylpiperazine moiety can enhance blood-brain barrier penetration. Additionally, it finds application in the production of small molecule inhibitors for enzymes and receptors, contributing to drug discovery efforts in oncology and other therapeutic areas. Its hydrochloride form ensures stability and solubility, making it suitable for use in organic synthesis and medicinal chemistry research.

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...