(S)-Ethyl 2-amino-3,3-dimethylbutanoate hydrochloride

95%

Reagent Code: #38250
fingerprint
CAS Number 144054-74-0

science Other reagents with same CAS 144054-74-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.6870 g/mol
Formula C₈H₁₈ClNO₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical synthesis industries. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs), particularly those targeting neurological and cardiovascular disorders. Its chiral nature makes it valuable in the synthesis of enantiomerically pure drugs, enhancing their efficacy and reducing side effects. Additionally, it is employed in the development of peptidomimetics and other bioactive molecules, contributing to advancements in drug discovery and medicinal chemistry. Its stability and reactivity also make it suitable for use in organic synthesis, particularly in the construction of complex molecular architectures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,201.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-Ethyl 2-amino-3,3-dimethylbutanoate hydrochloride
No image available

This compound is primarily utilized in the pharmaceutical and chemical synthesis industries. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs), particularly those targeting neurological and cardiovascular disorders. Its chiral nature makes it valuable in the synthesis of enantiomerically pure drugs, enhancing their efficacy and reducing side effects. Additionally, it is employed in the development of peptidomimetics and other bioactive molecules, contri

This compound is primarily utilized in the pharmaceutical and chemical synthesis industries. It serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs), particularly those targeting neurological and cardiovascular disorders. Its chiral nature makes it valuable in the synthesis of enantiomerically pure drugs, enhancing their efficacy and reducing side effects. Additionally, it is employed in the development of peptidomimetics and other bioactive molecules, contributing to advancements in drug discovery and medicinal chemistry. Its stability and reactivity also make it suitable for use in organic synthesis, particularly in the construction of complex molecular architectures.

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...