(S)-Methyl 3-(1-amino-2-hydroxyethyl)benzoate hydrochloride

97%

Reagent Code: #235694
fingerprint
CAS Number 1391447-69-0

science Other reagents with same CAS 1391447-69-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.68 g/mol
Formula C₁₀H₁₄ClNO₃
badge Registry Numbers
MDL Number MFCD12910849
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used in the synthesis of β-blockers, particularly in the production of chiral intermediates for pharmaceuticals. Its enantiomerically pure structure makes it valuable in creating active pharmaceutical ingredients (APIs) that require high stereochemical precision, such as cardiovascular drugs. Commonly employed in asymmetric synthesis routes where the hydroxy and amino functional groups allow for further chemical modifications. Also utilized in research settings for developing novel adrenergic receptor antagonists.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,180.00
inventory 250mg
10-20 days ฿38,330.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-Methyl 3-(1-amino-2-hydroxyethyl)benzoate hydrochloride
No image available

Used in the synthesis of β-blockers, particularly in the production of chiral intermediates for pharmaceuticals. Its enantiomerically pure structure makes it valuable in creating active pharmaceutical ingredients (APIs) that require high stereochemical precision, such as cardiovascular drugs. Commonly employed in asymmetric synthesis routes where the hydroxy and amino functional groups allow for further chemical modifications. Also utilized in research settings for developing novel adrenergic receptor an

Used in the synthesis of β-blockers, particularly in the production of chiral intermediates for pharmaceuticals. Its enantiomerically pure structure makes it valuable in creating active pharmaceutical ingredients (APIs) that require high stereochemical precision, such as cardiovascular drugs. Commonly employed in asymmetric synthesis routes where the hydroxy and amino functional groups allow for further chemical modifications. Also utilized in research settings for developing novel adrenergic receptor antagonists.

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...