(R)-1-Amino-3-chloropropan-2-ol hydrochloride

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Reagent Code: #230498
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CAS Number 34839-14-0

science Other reagents with same CAS 34839-14-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.02 g/mol
Formula C₃H₉Cl₂NO
badge Registry Numbers
MDL Number MFCD11113550
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-blockers like propranolol and other adrenergic blocking agents. Its chiral center allows for selective biological activity in final drug compounds. Also employed in the synthesis of other fine chemicals where enantiomeric purity is critical. Commonly utilized in research settings for asymmetric synthesis and development of optically active molecules.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿168.00
inventory 250mg
10-20 days ฿310.00
inventory 1g
10-20 days ฿450.00
inventory 5g
10-20 days ฿2,220.00
inventory 25g
10-20 days ฿9,500.00
inventory 100g
10-20 days ฿37,810.00

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(R)-1-Amino-3-chloropropan-2-ol hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-blockers like propranolol and other adrenergic blocking agents. Its chiral center allows for selective biological activity in final drug compounds. Also employed in the synthesis of other fine chemicals where enantiomeric purity is critical. Commonly utilized in research settings for asymmetric synthesis and development of optically active molecules.

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-blockers like propranolol and other adrenergic blocking agents. Its chiral center allows for selective biological activity in final drug compounds. Also employed in the synthesis of other fine chemicals where enantiomeric purity is critical. Commonly utilized in research settings for asymmetric synthesis and development of optically active molecules.

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