string(7) "reagent" (S)-(-)-2-Acetoxypropionyl Chloride

(S)-(-)-2-Acetoxypropionyl Chloride

98%

Reagent Code: #235282
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CAS Number 36394-75-9

science Other reagents with same CAS 36394-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.56 g/mol
Formula C₅H₇ClO₃
badge Registry Numbers
MDL Number MFCD00145252
thermostat Physical Properties
Boiling Point 78°C/22mmHg(lit.)
inventory_2 Storage & Handling
Density 1.19g/ml
Storage 2-8°C, stored in inert gas

description Product Description

Used primarily as a chiral acylating agent in the synthesis of optically active pharmaceuticals and fine chemicals. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in producing enantiomerically pure compounds. Commonly employed in the preparation of esters and amides where retention of configuration is critical. Frequently utilized in the development of beta-blockers and other bioactive molecules requiring specific chirality for activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,190.00
inventory 1g
10-20 days ฿2,450.00
inventory 25g
10-20 days ฿49,980.00
inventory 100g
10-20 days ฿150,390.00
inventory 5g
10-20 days ฿10,180.00

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(S)-(-)-2-Acetoxypropionyl Chloride
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Used primarily as a chiral acylating agent in the synthesis of optically active pharmaceuticals and fine chemicals. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in producing enantiomerically pure compounds. Commonly employed in the preparation of esters and amides where retention of configuration is critical. Frequently utilized in the development of beta-blockers and other bioactive molecules requiring specific chirality for activity.

Used primarily as a chiral acylating agent in the synthesis of optically active pharmaceuticals and fine chemicals. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in producing enantiomerically pure compounds. Commonly employed in the preparation of esters and amides where retention of configuration is critical. Frequently utilized in the development of beta-blockers and other bioactive molecules requiring specific chirality for activity.

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