2,4-Dinitrobenzylbromide

95%

Reagent Code: #43829
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CAS Number 3013-38-5

science Other reagents with same CAS 3013-38-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.0296 g/mol
Formula C₇H₅BrN₂O₄
badge Registry Numbers
MDL Number MFCD00792410
thermostat Physical Properties
Melting Point 50-52 °C
Boiling Point 360.3 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.830±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key reagent for introducing the 2,4-dinitrobenzyl protecting group, particularly for alcohols and amines. Its application is crucial in peptide chemistry, where it protects functional groups during complex reactions, ensuring selective transformations. Additionally, it is employed in the preparation of fluorescent probes and as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its reactivity with nucleophiles makes it valuable in creating derivatives for analytical and research purposes.

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Test Parameter Specification
Appearance solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure
Note Low melting point solid, may change state in different environments (solid, liquid or semi-solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,860.00
inventory 1g
10-20 days ฿26,640.00

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2,4-Dinitrobenzylbromide
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Used primarily in organic synthesis, this compound serves as a key reagent for introducing the 2,4-dinitrobenzyl protecting group, particularly for alcohols and amines. Its application is crucial in peptide chemistry, where it protects functional groups during complex reactions, ensuring selective transformations. Additionally, it is employed in the preparation of fluorescent probes and as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its reactivity with nucleophiles make

Used primarily in organic synthesis, this compound serves as a key reagent for introducing the 2,4-dinitrobenzyl protecting group, particularly for alcohols and amines. Its application is crucial in peptide chemistry, where it protects functional groups during complex reactions, ensuring selective transformations. Additionally, it is employed in the preparation of fluorescent probes and as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its reactivity with nucleophiles makes it valuable in creating derivatives for analytical and research purposes.

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