Diethyl 2,5-dibromoterephthalate

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Reagent Code: #170000
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CAS Number 18013-97-3

science Other reagents with same CAS 18013-97-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 380.03 g/mol
Formula C₁₂H₁₂Br₂O₄
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of functional organic materials, particularly in the preparation of conjugated polymers and metal-organic frameworks (MOFs). Its brominated aromatic structure enables cross-coupling reactions, such as Suzuki or Heck reactions, allowing the introduction of various functional groups for advanced material design. Also employed in the development of flame-retardant compounds due to the presence of bromine atoms. Its ester groups provide sites for further chemical modification, making it valuable in pharmaceutical and agrochemical research for building complex molecular architectures.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿162.00
5g
10-20 days ฿540.00
25g
10-20 days ฿1,670.00
100g
10-20 days ฿5,940.00
500g
10-20 days ฿29,230.00

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Diethyl 2,5-dibromoterephthalate
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Used as a key intermediate in the synthesis of functional organic materials, particularly in the preparation of conjugated polymers and metal-organic frameworks (MOFs). Its brominated aromatic structure enables cross-coupling reactions, such as Suzuki or Heck reactions, allowing the introduction of various functional groups for advanced material design. Also employed in the development of flame-retardant compounds due to the presence of bromine atoms. Its ester groups provide sites for further chemical m

Used as a key intermediate in the synthesis of functional organic materials, particularly in the preparation of conjugated polymers and metal-organic frameworks (MOFs). Its brominated aromatic structure enables cross-coupling reactions, such as Suzuki or Heck reactions, allowing the introduction of various functional groups for advanced material design. Also employed in the development of flame-retardant compounds due to the presence of bromine atoms. Its ester groups provide sites for further chemical modification, making it valuable in pharmaceutical and agrochemical research for building complex molecular architectures.

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