1-(6-Nitrobenzo[d][1,3]dioxol-5-yl)ethyl Carbonochloridate

≥95%

Reagent Code: #220336
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CAS Number 156876-26-5

science Other reagents with same CAS 156876-26-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.62 g/mol
Formula C₁₀H₈ClNO₆
badge Registry Numbers
MDL Number MFCD05864010
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nitrobenzodioxole-based drugs. Its reactive chloroformate group enables coupling reactions with amines or alcohols, making it valuable for constructing carbonate or carbamate linkages in bioactive molecules. Commonly applied in medicinal chemistry for modifying drug candidates to enhance metabolic stability or binding affinity. Also utilized in the preparation of prodrugs and enzyme inhibitors due to its ability to mask functional groups.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿27,000.00
inventory 1g
10-20 days ฿35,700.00
1-(6-Nitrobenzo[d][1,3]dioxol-5-yl)ethyl Carbonochloridate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nitrobenzodioxole-based drugs. Its reactive chloroformate group enables coupling reactions with amines or alcohols, making it valuable for constructing carbonate or carbamate linkages in bioactive molecules. Commonly applied in medicinal chemistry for modifying drug candidates to enhance metabolic stability or binding affinity. Also utilized in the preparation of prodrugs and enzyme inhibitors due to

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nitrobenzodioxole-based drugs. Its reactive chloroformate group enables coupling reactions with amines or alcohols, making it valuable for constructing carbonate or carbamate linkages in bioactive molecules. Commonly applied in medicinal chemistry for modifying drug candidates to enhance metabolic stability or binding affinity. Also utilized in the preparation of prodrugs and enzyme inhibitors due to its ability to mask functional groups.

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