4-Chlorophenyl Chloroformate

98%

Reagent Code: #159928
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CAS Number 7693-45-0

science Other reagents with same CAS 7693-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.01 g/mol
Formula C₇H₄Cl₂O₂
badge Registry Numbers
MDL Number MFCD00000638
thermostat Physical Properties
Boiling Point 100-102°C 12mm Hg (Lit.)
inventory_2 Storage & Handling
Density 1.3650 g/cm3
Storage 2-8℃, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It reacts readily with amines and alcohols to form carbamates and carbonates, which are key structural motifs in various bioactive molecules. Commonly employed in the preparation of protecting groups for amines due to its selective reactivity. Also utilized in the synthesis of pesticides and herbicides, where it helps build complex ester and amide linkages. Its chloroformate group acts as an activating agent in peptide coupling and other condensation reactions. Handle with care due to its moisture sensitivity and potential lachrymatory effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,210.00
inventory 5g
10-20 days ฿5,500.00
inventory 25g
10-20 days ฿16,380.00

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4-Chlorophenyl Chloroformate
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It reacts readily with amines and alcohols to form carbamates and carbonates, which are key structural motifs in various bioactive molecules. Commonly employed in the preparation of protecting groups for amines due to its selective reactivity. Also utilized in the synthesis of pesticides and herbicides, where it helps build complex ester and amide linkages. Its chloroformate group acts as

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It reacts readily with amines and alcohols to form carbamates and carbonates, which are key structural motifs in various bioactive molecules. Commonly employed in the preparation of protecting groups for amines due to its selective reactivity. Also utilized in the synthesis of pesticides and herbicides, where it helps build complex ester and amide linkages. Its chloroformate group acts as an activating agent in peptide coupling and other condensation reactions. Handle with care due to its moisture sensitivity and potential lachrymatory effects.

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