3',3'-Dimethyl-6-nitro-1'-(2-(pent-4-enoyloxy)ethyl)spiro[chromene-2,2'-indolin]-8-yl pent-4-enoate

95%

Reagent Code: #179254
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CAS Number 1554286-40-6

science Other reagents with same CAS 1554286-40-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 532.58 g/mol
Formula C₃₀H₃₂N₂O₇
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a photochromic compound in specialty optical materials, particularly in the development of light-responsive lenses and coatings. Its spiro structure enables reversible ring-opening under UV light, resulting in a visible color change, making it suitable for applications in smart windows, ophthalmic lenses, and sensors. The presence of nitro and ester groups enhances photoresponsiveness and thermal stability. The pent-4-enoyloxy side chains allow for covalent incorporation into polymer matrices through crosslinking, improving durability and fatigue resistance in final products.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,780.00
inventory 250mg
10-20 days ฿23,410.00
inventory 1g
10-20 days ฿77,580.00

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3',3'-Dimethyl-6-nitro-1'-(2-(pent-4-enoyloxy)ethyl)spiro[chromene-2,2'-indolin]-8-yl pent-4-enoate
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Used as a photochromic compound in specialty optical materials, particularly in the development of light-responsive lenses and coatings. Its spiro structure enables reversible ring-opening under UV light, resulting in a visible color change, making it suitable for applications in smart windows, ophthalmic lenses, and sensors. The presence of nitro and ester groups enhances photoresponsiveness and thermal stability. The pent-4-enoyloxy side chains allow for covalent incorporation into polymer matrices thr

Used as a photochromic compound in specialty optical materials, particularly in the development of light-responsive lenses and coatings. Its spiro structure enables reversible ring-opening under UV light, resulting in a visible color change, making it suitable for applications in smart windows, ophthalmic lenses, and sensors. The presence of nitro and ester groups enhances photoresponsiveness and thermal stability. The pent-4-enoyloxy side chains allow for covalent incorporation into polymer matrices through crosslinking, improving durability and fatigue resistance in final products.

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