1548-77-2

Basic information

• Product Name: Benzenemethanamine, 2,3,4,5,6-pentafluoro-
• CAS NO: 1548-77-2
• Molecular Formula: C7H4F5N
• Molecular Weight: 197.107
• Mol File: 1548-77-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenemethanamine, 2,3,4,5,6-pentafluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, 2,3,4,5,6-pentafluoro-(1548-77-2)
• EPA Substance Registry System: Benzenemethanamine, 2,3,4,5,6-pentafluoro-(1548-77-2)

Safety Data

• Hazardous Substances Data: 1548-77-2(Hazardous Substances Data)

Upstream product

• 158388-55-7 N-(benzylidene)-2,3,4,5,6-pentafluorobenzylamine 
• 1765-40-8 (bromomethyl)pentafluorobenzene 
• 773-82-0 Pentafluorobenzonitrile 
• 652-31-3 2,3,4,5,6-pentafluorobenzamide 
• 2561-28-6 2-((perfluorophenyl)methyl)isoindoline-1,3-dione 

Downstream Products

• 1452162-38-7 3-hydroxy-3-methyl-5-oxo-5-(((perfluorophenyl)methyl)amino)pentyl acetate 
• 1452162-39-8 3-methyl-5-oxo-5-(((perfluorophenyl)methyl)amino)pentane-1,3-diyl diacetate 
• 1452162-37-6 3,5-Dihydroxy-3-methyl-N-((perfluorophenyl)methyl)pentanamide 
• 1443546-94-8 4-isobutoxy-8-(pentafluorobenzamido)-N-(pentafluorobenzyl)quinoline-2-carboxamide 
• 1443546-93-7 4-isobutoxy-N-(pentafluorobenzyl)-8-(pentafluorophenylureido)quinoline-2-carboxamide 
• 1443546-91-5 4-isobutoxy-N-(pentafluorobenzyl)-8-(pentafluorobenzylthioureido)-quinoline-2-carboxamide 
• 1443546-89-1 4-isobutoxy-N-(pentafluorobenzyl)-8-(pentafluorophenylthioureido)-quinoline-2-carboxamide 
• 1443546-96-0 4-isobutoxy-8-(benzamido)-N-(pentafluorobenzyl)quinoline-2-carboxamide 
• 1443546-99-3 4-isobutoxy-8-nitro-N-(pentafluorobenzyl)quinoline-2-carboxamide 
• 1254173-63-1 N,N'-bis(pentafluorophenylmethyl)-2-amino-4-imino-pent-2-ene 
• 1079759-04-8 N,N'-bis(2,3,4,5,6-pentafluorobenzyl)-1,7-dibromo-perylene-3,4:9,10-bis(dicarboximide) 
• 235102-00-8 C₂₄H₁₉F₅N₂O₇S 
• 440-60-8 (2,3,4,5,6-pentafluorophenyl)methanol 

Relevant articles and documents

A superhydrophobic zeolitic imidazolate framework (ZIF-90) with high steam stability for efficient recovery of bioalcohols

A superhydrophobic zeolitic imidazolate framework (ZIF-90) with high steam stability is prepared through post-functionalization via an amine condensation reaction. The developed superhydrophobic ZIF-90 is highly promising as an effective and reusable adsorbent for bio-alcohol recovery.

Organic n-channel transistors based on core-cyanated perylene carboxylic diimide derivatives

Five core-cyanated perylene carboxylic diimides end-functionalized with fluorine-containing linear and cyclic substituents have been synthesized and employed in the fabrication of air-stable n-channel organic thin-film field-effect transistors with carrier mobilities up to 0.1 cm2/Vs. The relationships between molecular structure, thin-film morphology, substrate temperature during vacuum deposition, transistor performance, and air stability have been investigated. Our experiments led us to conclude that the role of the fluorine functionalization in the air-stable n-channel operation of the transistors is different than previously thought.

The pattern of fluorine substitution affects binding affinity in a small library of fluoroaromatic inhibitors for carbonic anhydrase

(equation presented) A library of fluoroaromatic inhibitors of carbonic anhydrase has been found to bind in a manner dependent on both hydrophobicity and the pattern of substitution of the fluoroaromatic ring. All of the compounds in the library bind to the protein with Kd 3 nM. We have inferred two distinct binding modes from our data, which suggest two types of interactions that should be considered when designing fluorinated drugs.