methanesulfonic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl) ester

Reagent Code: #51124
fingerprint
CAS Number 1049637-71-9

science Other reagents with same CAS 1049637-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.27 g/mol
Formula C₈H₁₅NO₃S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily in organic synthesis, this chiral mesylate ester serves as a building block for the preparation of various pharmaceuticals. It is particularly valuable in the synthesis of complex molecules where stereochemistry plays a crucial role, such as drugs targeting the central nervous system. The compound leverages its structural properties to build molecules that interact with specific receptors. Its excellent leaving group ability, stability, and reactivity make it a preferred choice in the production of enantiomerically pure active pharmaceutical ingredients with minimal side effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
methanesulfonic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl) ester
No image available

Used primarily in organic synthesis, this chiral mesylate ester serves as a building block for the preparation of various pharmaceuticals. It is particularly valuable in the synthesis of complex molecules where stereochemistry plays a crucial role, such as drugs targeting the central nervous system. The compound leverages its structural properties to build molecules that interact with specific receptors. Its excellent leaving group ability, stability, and reactivity make it a preferred choice in the prod

Used primarily in organic synthesis, this chiral mesylate ester serves as a building block for the preparation of various pharmaceuticals. It is particularly valuable in the synthesis of complex molecules where stereochemistry plays a crucial role, such as drugs targeting the central nervous system. The compound leverages its structural properties to build molecules that interact with specific receptors. Its excellent leaving group ability, stability, and reactivity make it a preferred choice in the production of enantiomerically pure active pharmaceutical ingredients with minimal side effects.

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...