O-Formyl-D-mandeloyl Chloride

97 %

Reagent Code: #221476
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CAS Number 29169-64-0

science Other reagents with same CAS 29169-64-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.60 g/mol
Formula C₉H₇ClO₃
badge Registry Numbers
MDL Number MFCD00799229
thermostat Physical Properties
Boiling Point 221°C (Lit.)
inventory_2 Storage & Handling
Density 1.2900 g/cm3
Storage 2-8℃, dry

description Product Description

Used as an intermediate in the synthesis of chiral pharmaceuticals and fine chemicals, particularly in the preparation of optically active esters and amides. Its reactivity allows for selective acylation under mild conditions, making it valuable in asymmetric synthesis. Commonly employed in the development of antibiotics and enzyme inhibitors due to its ability to form stable derivatives with amines and alcohols. Also utilized in peptide mimetic construction where stereochemistry plays a critical role in biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿330.00
5g
10-20 days ฿1,130.00
25g
10-20 days ฿3,070.00
100g
10-20 days ฿8,390.00
O-Formyl-D-mandeloyl Chloride
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Used as an intermediate in the synthesis of chiral pharmaceuticals and fine chemicals, particularly in the preparation of optically active esters and amides. Its reactivity allows for selective acylation under mild conditions, making it valuable in asymmetric synthesis. Commonly employed in the development of antibiotics and enzyme inhibitors due to its ability to form stable derivatives with amines and alcohols. Also utilized in peptide mimetic construction where stereochemistry plays a critical role in

Used as an intermediate in the synthesis of chiral pharmaceuticals and fine chemicals, particularly in the preparation of optically active esters and amides. Its reactivity allows for selective acylation under mild conditions, making it valuable in asymmetric synthesis. Commonly employed in the development of antibiotics and enzyme inhibitors due to its ability to form stable derivatives with amines and alcohols. Also utilized in peptide mimetic construction where stereochemistry plays a critical role in biological activity.

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