(S)-Methyl 3-amino-3-(4-bromophenyl)propanoate hydrochloride

≥95%

Reagent Code: #38441
fingerprint
CAS Number 1245606-63-6

science Other reagents with same CAS 1245606-63-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.57 g/mol
Formula C₁₀H₁₃BrClNO₂
badge Registry Numbers
MDL Number MFCD12911008
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in pharmaceutical research and development as a chiral building block for the synthesis of various bioactive molecules. Its structure, featuring a 4-bromophenyl group, a primary amino group, and a methyl ester functionality as the hydrochloride salt, makes it valuable in the creation of enantiomerically pure compounds, which are crucial in drug design to ensure specificity and efficacy. It is often employed in the preparation of intermediates for potential therapeutic agents, particularly those targeting neurological and psychiatric disorders. Additionally, its chiral nature allows for studies in asymmetric synthesis, aiding in the development of more efficient and selective chemical processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,164.00
inventory 250mg
10-20 days ฿14,337.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-Methyl 3-amino-3-(4-bromophenyl)propanoate hydrochloride
No image available

This compound is primarily utilized in pharmaceutical research and development as a chiral building block for the synthesis of various bioactive molecules. Its structure, featuring a 4-bromophenyl group, a primary amino group, and a methyl ester functionality as the hydrochloride salt, makes it valuable in the creation of enantiomerically pure compounds, which are crucial in drug design to ensure specificity and efficacy. It is often employed in the preparation of intermediates for potential therapeutic

This compound is primarily utilized in pharmaceutical research and development as a chiral building block for the synthesis of various bioactive molecules. Its structure, featuring a 4-bromophenyl group, a primary amino group, and a methyl ester functionality as the hydrochloride salt, makes it valuable in the creation of enantiomerically pure compounds, which are crucial in drug design to ensure specificity and efficacy. It is often employed in the preparation of intermediates for potential therapeutic agents, particularly those targeting neurological and psychiatric disorders. Additionally, its chiral nature allows for studies in asymmetric synthesis, aiding in the development of more efficient and selective chemical processes.

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...