(S)-2-Chloro-3-phenylpropan-1-ol

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Reagent Code: #235678
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CAS Number 127180-75-0

science Other reagents with same CAS 127180-75-0

blur_circular Chemical Specifications

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Weight 170.64 g/mol
Formula C₉H₁₁ClO
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers and other cardiovascular drugs. Its stereochemistry allows for selective interactions in asymmetric synthesis, making it valuable in developing enantiomerically pure compounds. Also employed in the preparation of intermediates for anti-hypertensive agents and in the research of enzyme inhibitors. The presence of both chlorine and hydroxyl functional groups enables diverse chemical transformations, facilitating its use in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿18,760.00
inventory 100mg
10-20 days ฿37,530.00

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(S)-2-Chloro-3-phenylpropan-1-ol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers and other cardiovascular drugs. Its stereochemistry allows for selective interactions in asymmetric synthesis, making it valuable in developing enantiomerically pure compounds. Also employed in the preparation of intermediates for anti-hypertensive agents and in the research of enzyme inhibitors. The presence of both chlorine and hydroxyl functional groups enables diverse chemical transformat

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers and other cardiovascular drugs. Its stereochemistry allows for selective interactions in asymmetric synthesis, making it valuable in developing enantiomerically pure compounds. Also employed in the preparation of intermediates for anti-hypertensive agents and in the research of enzyme inhibitors. The presence of both chlorine and hydroxyl functional groups enables diverse chemical transformations, facilitating its use in multi-step organic syntheses.

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