2-Nitrobenzyl bromide

97%

Reagent Code: #116980
label
Alias 2-nitrobenzyl bromide; o-nitrobenzyl bromide
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CAS Number 3958-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.03 g/mol
Formula C₇H₆BrNO₂
badge Registry Numbers
EC Number 223-558-9
MDL Number MFCD00007184
thermostat Physical Properties
Melting Point 44-46 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used primarily in organic synthesis as a photolabile protecting group for carboxylic acids, alcohols, and amines. It is particularly valuable in the development of photoresponsive materials and controlled-release systems, where light-induced deprotection is required. In peptide chemistry, it serves as a temporary protecting group that can be removed under mild conditions using UV light, minimizing damage to sensitive structures. Additionally, it finds applications in the preparation of photoactivatable probes and caged compounds for biochemical studies, enabling precise spatial and temporal control over the release of active molecules.

format_list_bulleted Product Specification

Test Parameter Specification
Melting Point 45-48
Purity (GC) 97-100%
Appearance Yellow to Tan Powder
Infrared Spectrum Conforms To Structure
Note Low Melting Point Solid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,500.00
inventory 5g
10-20 days ฿350.00
inventory 500g
10-20 days ฿29,370.00
inventory 100g
10-20 days ฿5,900.00
2-Nitrobenzyl bromide
Used primarily in organic synthesis as a photolabile protecting group for carboxylic acids, alcohols, and amines. It is particularly valuable in the development of photoresponsive materials and controlled-release systems, where light-induced deprotection is required. In peptide chemistry, it serves as a temporary protecting group that can be removed under mild conditions using UV light, minimizing damage to sensitive structures. Additionally, it finds applications in the preparation of photoactivatable probes and caged compounds for biochemical studies, enabling precise spatial and temporal control over the release of active molecules.
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