P-TOLYL CHLOROFORMATE

97%

Reagent Code: #226671
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CAS Number 937-62-2

science Other reagents with same CAS 937-62-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.59 g/mol
Formula C₈H₇ClO₂
badge Registry Numbers
MDL Number MFCD00013255
thermostat Physical Properties
Boiling Point 99.5 °C/20 mmHg (lit.)
inventory_2 Storage & Handling
Density 1.188 g/mL at 25 °C (lit.)
Storage 2-8°C

description Product Description

Used primarily as a reagent in organic synthesis, particularly in the protection of functional groups such as amines and alcohols. Its reactivity allows it to form carbamate or carbonate derivatives, which are stable under various reaction conditions but can be removed selectively when needed. Commonly employed in peptide synthesis and pharmaceutical intermediates where controlled protection-deprotection strategies are required. Also utilized in the preparation of agrochemicals and specialty polymers due to its ability to modify molecular structure with an aromatic methyl-substituted phenyl group. Handling requires caution due to its lachrymatory and moisture-sensitive properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿770.00
1g
10-20 days ฿2,580.00
P-TOLYL CHLOROFORMATE
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Used primarily as a reagent in organic synthesis, particularly in the protection of functional groups such as amines and alcohols. Its reactivity allows it to form carbamate or carbonate derivatives, which are stable under various reaction conditions but can be removed selectively when needed. Commonly employed in peptide synthesis and pharmaceutical intermediates where controlled protection-deprotection strategies are required. Also utilized in the preparation of agrochemicals and specialty polymers due

Used primarily as a reagent in organic synthesis, particularly in the protection of functional groups such as amines and alcohols. Its reactivity allows it to form carbamate or carbonate derivatives, which are stable under various reaction conditions but can be removed selectively when needed. Commonly employed in peptide synthesis and pharmaceutical intermediates where controlled protection-deprotection strategies are required. Also utilized in the preparation of agrochemicals and specialty polymers due to its ability to modify molecular structure with an aromatic methyl-substituted phenyl group. Handling requires caution due to its lachrymatory and moisture-sensitive properties.

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