2-Naphthyl Chloroformate

97%

Reagent Code: #217735
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CAS Number 7693-50-7

science Other reagents with same CAS 7693-50-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.63 g/mol
Formula C₁₁H₇ClO₂
badge Registry Numbers
MDL Number MFCD00060059
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used primarily as a derivatizing agent in organic synthesis, particularly in the protection of amines and alcohols during multi-step reactions. It reacts selectively with primary and secondary amines to form stable carbamate derivatives, which are useful in peptide synthesis and pharmaceutical manufacturing. Also employed in the preparation of active esters for coupling reactions. Its bulky aromatic structure enhances steric hindrance, improving selectivity in complex molecule assembly. Commonly applied in analytical chemistry to modify polar functional groups for better chromatographic separation, especially in HPLC and GC analysis. Additionally, it serves as an intermediate in the synthesis of dyes, agrochemicals, and certain specialty polymers.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿9,060.00
2-Naphthyl Chloroformate
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Used primarily as a derivatizing agent in organic synthesis, particularly in the protection of amines and alcohols during multi-step reactions. It reacts selectively with primary and secondary amines to form stable carbamate derivatives, which are useful in peptide synthesis and pharmaceutical manufacturing. Also employed in the preparation of active esters for coupling reactions. Its bulky aromatic structure enhances steric hindrance, improving selectivity in complex molecule assembly. Commonly applied

Used primarily as a derivatizing agent in organic synthesis, particularly in the protection of amines and alcohols during multi-step reactions. It reacts selectively with primary and secondary amines to form stable carbamate derivatives, which are useful in peptide synthesis and pharmaceutical manufacturing. Also employed in the preparation of active esters for coupling reactions. Its bulky aromatic structure enhances steric hindrance, improving selectivity in complex molecule assembly. Commonly applied in analytical chemistry to modify polar functional groups for better chromatographic separation, especially in HPLC and GC analysis. Additionally, it serves as an intermediate in the synthesis of dyes, agrochemicals, and certain specialty polymers.

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