1-(9H-Fluoren-9-yl)-2,2-dimethylpropan-1-one

95%

Reagent Code: #59476
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CAS Number 786657-15-6

science Other reagents with same CAS 786657-15-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.33 g/mol
Formula C₁₈H₁₈O
badge Registry Numbers
MDL Number MFCD00028850
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

This chemical is primarily used in the field of organic synthesis, particularly as a photoremovable protecting group for carboxylic acids and other functional groups. Its fluorenyl group allows for efficient deprotection under UV light, making it valuable in photolithography and the development of light-sensitive materials. Additionally, it finds application in peptide synthesis, where it helps protect specific amino acids during the formation of peptide bonds. Its stability under various reaction conditions and ease of removal make it a versatile tool in advanced chemical research and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,480.00
inventory 250mg
10-20 days ฿12,960.00

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1-(9H-Fluoren-9-yl)-2,2-dimethylpropan-1-one
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This chemical is primarily used in the field of organic synthesis, particularly as a photoremovable protecting group for carboxylic acids and other functional groups. Its fluorenyl group allows for efficient deprotection under UV light, making it valuable in photolithography and the development of light-sensitive materials. Additionally, it finds application in peptide synthesis, where it helps protect specific amino acids during the formation of peptide bonds. Its stability under various reaction condit

This chemical is primarily used in the field of organic synthesis, particularly as a photoremovable protecting group for carboxylic acids and other functional groups. Its fluorenyl group allows for efficient deprotection under UV light, making it valuable in photolithography and the development of light-sensitive materials. Additionally, it finds application in peptide synthesis, where it helps protect specific amino acids during the formation of peptide bonds. Its stability under various reaction conditions and ease of removal make it a versatile tool in advanced chemical research and material science.

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