methyl 2,5-dibromo-3-nitrobenzoate

98%

Reagent Code: #40921
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CAS Number 124371-59-1

science Other reagents with same CAS 124371-59-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.5000 g/mol
Formula C₈H₅BrClNO₄
badge Registry Numbers
MDL Number MFCD12172987
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Primarily used in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of complex molecules. Additionally, it is utilized in research settings for studying nitration and bromination reactions, aiding in the understanding of reaction mechanisms and the design of new synthetic pathways. Its nitro and ester groups also make it a candidate for applications in material science, particularly in the creation of specialized polymers or coatings.

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Test Parameter Specification
Appearance Yellow powder
Purity (%) 97.5-100%
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿666.00

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methyl 2,5-dibromo-3-nitrobenzoate
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Primarily used in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of complex molecules. Additionally, it is utilized in research settings for studying nitration and bromination reactions, aiding in the understanding of reaction mechanisms and the design of new synthetic pathways. Its nitro and ester groups also make it a candidate for appl

Primarily used in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of complex molecules. Additionally, it is utilized in research settings for studying nitration and bromination reactions, aiding in the understanding of reaction mechanisms and the design of new synthetic pathways. Its nitro and ester groups also make it a candidate for applications in material science, particularly in the creation of specialized polymers or coatings.

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