1-Phenylethyl chloroformate

95%

Reagent Code: #123921
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CAS Number 15600-32-5

science Other reagents with same CAS 15600-32-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.62 g/mol
Formula C₉H₉ClO₂
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MDL Number MFCD24141103
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

1-Phenylethyl chloroformate is widely used in organic synthesis as a reagent for the protection of amines. It is particularly effective in the formation of carbamates, which are crucial intermediates in the production of pharmaceuticals and agrochemicals. The compound is also employed in peptide synthesis to protect amino groups, ensuring selective reactions at other functional sites. Additionally, it serves as a chiral derivatizing agent, aiding in the resolution of enantiomers for analytical purposes. Its application extends to the preparation of specialty chemicals, where it facilitates the introduction of the phenylethyl group into target molecules.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿29,196.00
inventory 250mg
10-20 days ฿3,096.00
inventory 1g
10-20 days ฿8,343.00

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1-Phenylethyl chloroformate
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1-Phenylethyl chloroformate is widely used in organic synthesis as a reagent for the protection of amines. It is particularly effective in the formation of carbamates, which are crucial intermediates in the production of pharmaceuticals and agrochemicals. The compound is also employed in peptide synthesis to protect amino groups, ensuring selective reactions at other functional sites. Additionally, it serves as a chiral derivatizing agent, aiding in the resolution of enantiomers for analytical purposes.

1-Phenylethyl chloroformate is widely used in organic synthesis as a reagent for the protection of amines. It is particularly effective in the formation of carbamates, which are crucial intermediates in the production of pharmaceuticals and agrochemicals. The compound is also employed in peptide synthesis to protect amino groups, ensuring selective reactions at other functional sites. Additionally, it serves as a chiral derivatizing agent, aiding in the resolution of enantiomers for analytical purposes. Its application extends to the preparation of specialty chemicals, where it facilitates the introduction of the phenylethyl group into target molecules.

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