4,5-Dimethoxy-2-nitrobenzyl carbonochloridate

≥95%

Reagent Code: #45904
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CAS Number 42855-00-5

science Other reagents with same CAS 42855-00-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.64 g/mol
Formula C₁₀H₁₀ClNO₆
badge Registry Numbers
MDL Number MFCD00143507
thermostat Physical Properties
Melting Point 125°C
Boiling Point 396.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Used primarily in organic synthesis, this compound serves as a protective group for alcohols and amines, enabling selective reactions in complex molecule construction. It is particularly valuable in peptide and carbohydrate chemistry, where temporary protection of functional groups is essential. Additionally, it finds application in photolabile protecting strategies, allowing controlled release of active molecules under light exposure, which is useful in drug delivery systems and photochemical studies. Its nitrobenzyl group facilitates cleavage upon UV irradiation, making it suitable for light-triggered applications in research and industrial processes.

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Test Parameter Specification
Appearance White to yellow solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,086.00
inventory 100mg
10-20 days ฿900.00
inventory 250mg
10-20 days ฿1,422.00
inventory 5g
10-20 days ฿14,382.00

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4,5-Dimethoxy-2-nitrobenzyl carbonochloridate
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Used primarily in organic synthesis, this compound serves as a protective group for alcohols and amines, enabling selective reactions in complex molecule construction. It is particularly valuable in peptide and carbohydrate chemistry, where temporary protection of functional groups is essential. Additionally, it finds application in photolabile protecting strategies, allowing controlled release of active molecules under light exposure, which is useful in drug delivery systems and photochemical studies. I

Used primarily in organic synthesis, this compound serves as a protective group for alcohols and amines, enabling selective reactions in complex molecule construction. It is particularly valuable in peptide and carbohydrate chemistry, where temporary protection of functional groups is essential. Additionally, it finds application in photolabile protecting strategies, allowing controlled release of active molecules under light exposure, which is useful in drug delivery systems and photochemical studies. Its nitrobenzyl group facilitates cleavage upon UV irradiation, making it suitable for light-triggered applications in research and industrial processes.

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