(3R,4S)-3-Amino-4-methylhexanoic acid

97%

Reagent Code: #36755
fingerprint
CAS Number 75946-24-6

science Other reagents with same CAS 75946-24-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.1995 g/mol
Formula C₇H₁₅NO₂
badge Registry Numbers
MDL Number MFCD17215345
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological disorders. It serves as a key intermediate in the production of GABA analogs, which are essential for creating medications that manage conditions like epilepsy, neuropathic pain, and anxiety. Additionally, its chiral structure makes it valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds for enhanced therapeutic efficacy. It is also explored in research for its potential role in designing novel bioactive molecules with applications in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,952.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3R,4S)-3-Amino-4-methylhexanoic acid
No image available

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological disorders. It serves as a key intermediate in the production of GABA analogs, which are essential for creating medications that manage conditions like epilepsy, neuropathic pain, and anxiety. Additionally, its chiral structure makes it valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds for enhanced therapeutic efficacy. It is al

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological disorders. It serves as a key intermediate in the production of GABA analogs, which are essential for creating medications that manage conditions like epilepsy, neuropathic pain, and anxiety. Additionally, its chiral structure makes it valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds for enhanced therapeutic efficacy. It is also explored in research for its potential role in designing novel bioactive molecules with applications in medicinal chemistry.

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...