(R)-Methyl 2-(pyrrolidin-3-yloxy)acetate 4-methylbenzenesulfonate

97%

Reagent Code: #113503
fingerprint
CAS Number 1965314-51-5

science Other reagents with same CAS 1965314-51-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.39 g/mol
Formula C₁₄H₂₁NO₆S
badge Registry Numbers
MDL Number MFCD30181969
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

Used in pharmaceutical research as a chiral building block for synthesizing biologically active compounds. Its structure is valuable in developing drugs targeting the central nervous system, particularly for neurological disorders. The compound’s chiral nature allows for the creation of enantiomerically pure substances, enhancing drug efficacy and reducing side effects. It is also employed in the development of prodrugs, where its ester group can be hydrolyzed to release active therapeutic agents. Additionally, it serves as an intermediate in organic synthesis for creating complex molecules with potential therapeutic applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,160.00
inventory 1g
10-20 days ฿4,725.00
inventory 100mg
10-20 days ฿1,350.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-Methyl 2-(pyrrolidin-3-yloxy)acetate 4-methylbenzenesulfonate
No image available

Used in pharmaceutical research as a chiral building block for synthesizing biologically active compounds. Its structure is valuable in developing drugs targeting the central nervous system, particularly for neurological disorders. The compound’s chiral nature allows for the creation of enantiomerically pure substances, enhancing drug efficacy and reducing side effects. It is also employed in the development of prodrugs, where its ester group can be hydrolyzed to release active therapeutic agents. Additi

Used in pharmaceutical research as a chiral building block for synthesizing biologically active compounds. Its structure is valuable in developing drugs targeting the central nervous system, particularly for neurological disorders. The compound’s chiral nature allows for the creation of enantiomerically pure substances, enhancing drug efficacy and reducing side effects. It is also employed in the development of prodrugs, where its ester group can be hydrolyzed to release active therapeutic agents. Additionally, it serves as an intermediate in organic synthesis for creating complex molecules with potential therapeutic applications.

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...