2-Ethoxy-4-formylphenyl 2,4-dichlorobenzoate

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Reagent Code: #180693
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CAS Number 444110-64-9

science Other reagents with same CAS 444110-64-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.18 g/mol
Formula C₁₆H₁₂Cl₂O₄
badge Registry Numbers
MDL Number MFCD03422508
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of photochromic compounds, particularly in the production of dyes and pigments that change color upon exposure to UV light. It plays a role in the development of light-sensitive materials for ophthalmic lenses, such as transition lenses. Also utilized in specialty polymers where controlled molecular cross-linking under light exposure is required. Its aldehyde and ester functional groups allow for further chemical modifications, making it valuable in organic synthesis for creating complex aromatic systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,250.00
inventory 250mg
10-20 days ฿5,490.00
inventory 1g
10-20 days ฿14,830.00

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2-Ethoxy-4-formylphenyl 2,4-dichlorobenzoate
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Used as an intermediate in the synthesis of photochromic compounds, particularly in the production of dyes and pigments that change color upon exposure to UV light. It plays a role in the development of light-sensitive materials for ophthalmic lenses, such as transition lenses. Also utilized in specialty polymers where controlled molecular cross-linking under light exposure is required. Its aldehyde and ester functional groups allow for further chemical modifications, making it valuable in organic synthe

Used as an intermediate in the synthesis of photochromic compounds, particularly in the production of dyes and pigments that change color upon exposure to UV light. It plays a role in the development of light-sensitive materials for ophthalmic lenses, such as transition lenses. Also utilized in specialty polymers where controlled molecular cross-linking under light exposure is required. Its aldehyde and ester functional groups allow for further chemical modifications, making it valuable in organic synthesis for creating complex aromatic systems.

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