Isopentyl Chloroformate

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Reagent Code: #200360
label
Alias 3-methylbutylchloroformate
fingerprint
CAS Number 628-50-2

science Other reagents with same CAS 628-50-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.60 g/mol
Formula C₆H₁₁ClO₂
badge Registry Numbers
MDL Number MFCD07776970
thermostat Physical Properties
Boiling Point 207.14 °C (rough estimate)
inventory_2 Storage & Handling
Density 1.0288
Storage 2-8°C

description Product Description

Used primarily as a reagent in organic synthesis, particularly in peptide and amino acid chemistry. It helps in the protection of functional groups such as amines by forming carbamate derivatives, which are stable under various reaction conditions but can be removed selectively when needed. Commonly employed in the preparation of active esters for coupling reactions, it facilitates the formation of amide bonds without racemization, making it valuable in solid-phase peptide synthesis. Also utilized in the production of pharmaceuticals and fine chemicals where controlled reactivity and selective transformations are required. Its volatility and reactivity demand careful handling, but its efficiency in introducing protecting groups makes it a preferred choice in complex molecule assembly.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,600.00
inventory 25g
10-20 days ฿64,510.00
inventory 5g
10-20 days ฿17,140.00
Isopentyl Chloroformate
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Used primarily as a reagent in organic synthesis, particularly in peptide and amino acid chemistry. It helps in the protection of functional groups such as amines by forming carbamate derivatives, which are stable under various reaction conditions but can be removed selectively when needed. Commonly employed in the preparation of active esters for coupling reactions, it facilitates the formation of amide bonds without racemization, making it valuable in solid-phase peptide synthesis. Also utilized in the

Used primarily as a reagent in organic synthesis, particularly in peptide and amino acid chemistry. It helps in the protection of functional groups such as amines by forming carbamate derivatives, which are stable under various reaction conditions but can be removed selectively when needed. Commonly employed in the preparation of active esters for coupling reactions, it facilitates the formation of amide bonds without racemization, making it valuable in solid-phase peptide synthesis. Also utilized in the production of pharmaceuticals and fine chemicals where controlled reactivity and selective transformations are required. Its volatility and reactivity demand careful handling, but its efficiency in introducing protecting groups makes it a preferred choice in complex molecule assembly.

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