(≥)-Camphanic acid chloride

95%

Reagent Code: #157230
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CAS Number 104530-16-7

science Other reagents with same CAS 104530-16-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.7124 g/mol
Formula C₁₁H₁₈ClO₂-
badge Registry Numbers
MDL Number MFCD00005534
thermostat Physical Properties
Melting Point 67-70 °C
Boiling Point 299.5±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.298±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as a chiral derivatizing agent in organic synthesis, especially for the resolution of racemic mixtures of alcohols and amines. Its ability to form diastereomeric esters or amides allows for separation by conventional techniques such as crystallization or chromatography. Commonly employed in the preparation of chiral auxiliaries and in asymmetric synthesis where stereochemical control is critical. Also utilized in the pharmaceutical industry for the purification and analysis of enantiomerically pure compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,600.00
inventory 1g
10-20 days ฿25,600.00

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(≥)-Camphanic acid chloride
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Used primarily as a chiral derivatizing agent in organic synthesis, especially for the resolution of racemic mixtures of alcohols and amines. Its ability to form diastereomeric esters or amides allows for separation by conventional techniques such as crystallization or chromatography. Commonly employed in the preparation of chiral auxiliaries and in asymmetric synthesis where stereochemical control is critical. Also utilized in the pharmaceutical industry for the purification and analysis of enantiomeric

Used primarily as a chiral derivatizing agent in organic synthesis, especially for the resolution of racemic mixtures of alcohols and amines. Its ability to form diastereomeric esters or amides allows for separation by conventional techniques such as crystallization or chromatography. Commonly employed in the preparation of chiral auxiliaries and in asymmetric synthesis where stereochemical control is critical. Also utilized in the pharmaceutical industry for the purification and analysis of enantiomerically pure compounds.

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