Decyl Chloroformate

95%

Reagent Code: #174457
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CAS Number 55488-51-2

science Other reagents with same CAS 55488-51-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.74 g/mol
Formula C₁₁H₂₁ClO₂
badge Registry Numbers
MDL Number MFCD00126853
thermostat Physical Properties
Boiling Point 163°C/44mmHg(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a protecting group reagent in organic synthesis, particularly in peptide synthesis. It selectively protects amino groups by forming carbamate derivatives, which are stable under a variety of reaction conditions but can be removed when needed. Its long alkyl chain enhances lipophilicity, making it useful in modifying solubility properties of intermediates in multi-step syntheses. Also employed in the preparation of activated esters and in pharmaceutical manufacturing where controlled protection-deprotection sequences are required.

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Size Availability Unit Price Quantity
inventory 1ml
10-20 days ฿700.00
inventory 5ml
10-20 days ฿3,010.00

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Decyl Chloroformate
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Used primarily as a protecting group reagent in organic synthesis, particularly in peptide synthesis. It selectively protects amino groups by forming carbamate derivatives, which are stable under a variety of reaction conditions but can be removed when needed. Its long alkyl chain enhances lipophilicity, making it useful in modifying solubility properties of intermediates in multi-step syntheses. Also employed in the preparation of activated esters and in pharmaceutical manufacturing where controlled pro

Used primarily as a protecting group reagent in organic synthesis, particularly in peptide synthesis. It selectively protects amino groups by forming carbamate derivatives, which are stable under a variety of reaction conditions but can be removed when needed. Its long alkyl chain enhances lipophilicity, making it useful in modifying solubility properties of intermediates in multi-step syntheses. Also employed in the preparation of activated esters and in pharmaceutical manufacturing where controlled protection-deprotection sequences are required.

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