(S)-Methyl 3-amino-3-(o-tolyl)propanoate hydrochloride

95%

Reagent Code: #38449
fingerprint
CAS Number 1245606-66-9

science Other reagents with same CAS 1245606-66-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.7032 g/mol
Formula C₁₁H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD12911022
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules due to its stereospecific structure. It serves as a key building block in the production of active pharmaceutical ingredients (APIs) for drugs targeting neurological and cardiovascular disorders. Its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. Additionally, it is employed in research settings for studying enzyme interactions and receptor binding, aiding in the discovery of new therapeutic agents. Its stability and reactivity also make it suitable for use in organic synthesis and medicinal chemistry projects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,882.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-Methyl 3-amino-3-(o-tolyl)propanoate hydrochloride
No image available

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules due to its stereospecific structure. It serves as a key building block in the production of active pharmaceutical ingredients (APIs) for drugs targeting neurological and cardiovascular disorders. Its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. Additionally, it is employed in research settings for st

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules due to its stereospecific structure. It serves as a key building block in the production of active pharmaceutical ingredients (APIs) for drugs targeting neurological and cardiovascular disorders. Its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. Additionally, it is employed in research settings for studying enzyme interactions and receptor binding, aiding in the discovery of new therapeutic agents. Its stability and reactivity also make it suitable for use in organic synthesis and medicinal chemistry projects.

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...