(S)-3-Bromo-2-hydroxy-2-methylpropanoic acid

95%

Reagent Code: #233546
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CAS Number 106089-20-7

science Other reagents with same CAS 106089-20-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183 g/mol
Formula C₄H₇BrO₃
badge Registry Numbers
MDL Number MFCD09750950
thermostat Physical Properties
Melting Point 113-114 °C
Boiling Point 294.5±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.831±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of beta-blockers, antimicrobials, enzyme inhibitors, and other cardiovascular drugs. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in producing enantiomerically pure compounds. Also employed in the preparation of agrochemicals and bioactive molecules where precise spatial arrangement of functional groups is critical. The hydroxyl, carboxylic acid, and bromomethyl groups enable further derivatization, such as nucleophilic substitution, esterification, or coupling reactions, facilitating its incorporation into more complex structures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,060.00
inventory 1g
10-20 days ฿8,450.00
inventory 5g
10-20 days ฿38,720.00
(S)-3-Bromo-2-hydroxy-2-methylpropanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of beta-blockers, antimicrobials, enzyme inhibitors, and other cardiovascular drugs. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in producing enantiomerically pure compounds. Also employed in the preparation of agrochemicals and bioactive molecules where precise spatial arrangement of functional groups is critical. The hydroxyl, carboxylic acid, and bromo

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of beta-blockers, antimicrobials, enzyme inhibitors, and other cardiovascular drugs. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in producing enantiomerically pure compounds. Also employed in the preparation of agrochemicals and bioactive molecules where precise spatial arrangement of functional groups is critical. The hydroxyl, carboxylic acid, and bromomethyl groups enable further derivatization, such as nucleophilic substitution, esterification, or coupling reactions, facilitating its incorporation into more complex structures.

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