1102-92-7

Basic information

• Product Name: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-
• Synonyms: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-
• CAS NO: 1102-92-7
• Molecular Formula: C₁₇H₈Cl₂F₆O₂
• Molecular Weight: 429
• Mol File: 1102-92-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-(1102-92-7)
• EPA Substance Registry System: Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis-(1102-92-7)

Safety Data

• Hazardous Substances Data: 1102-92-7(Hazardous Substances Data)

Usage

General Description

Benzoyl chloride, 4,4'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis- is a chemical compound that is commonly used as an intermediate or starting material in the synthesis of various organic compounds. It is a derivative of benzoyl chloride, and the addition of the 2,2,2-trifluoro-1-(trifluoromethyl)ethylidene group makes it a highly reactive and versatile compound. This chemical is utilized in the pharmaceutical, agrochemical, and manufacturing industries for the production of various organic compounds, including pharmaceuticals, pesticides, and polymers. Due to its reactivity and versatility, it is an important chemical in the field of organic synthesis.

Upstream product

• 1095-77-8 1,1,1,3,3,3-hexafluoro-2,2-di(p-tolyl)propane 
• 1171-47-7 2,2-bis(4-carboxyphenyl)hexafluoropropane 

Downstream Products

• 1346142-27-5 2,2-bis[4-(5-heptafluoropropyl-4-(4-pyridyl)oxazol-2-yl)phenyl]hexafluoropropane 
• 1346142-25-3 2,2-bis[4-(5-pentafluoroethyl-4-(4-pyridyl)oxazol-2-yl)phenyl]hexafluoropropane 

Relevant articles and documents

Preparation and properties of polybenzoxazole-based gas separation membranes: A comparative study between thermal rearrangement (TR) of poly(hydroxyimide) and thermal cyclodehydration of poly(hydroxyamide)

This comparative study focuses on the cyclodehydration reaction of poly(hydroxyamide)s (PHAs) and the thermal rearrangement (TR) reaction of aromatic poly(hydroxyimide)s (APIs) to produce polybenzoxazoles (PBOs) for application as gas separation membranes

Radical-forming polyamides for self-decontamination coatings

Design and synthesis of thermally stable polyamides with improved solubility based on an asymmetrical aromatic diamine containing phenoxy substituted benzophenone segment was the main objective of this work. These polymers were easily soluble at room temperature in polar aprotic solvents and even in less polar solvents, such as tetrahydrofuran. The polymers showed excellent thermal stability, up to 385°C, and exhibited glass transition in the range of 225-256°C. All the polymers emitted an intense blue light upon irradiation with UV light, due to the emission from the benzophenone chromophore. The free-standing films having the thickness in the range of tens of micrometers obtained from these polymers were flexible, tough, and maintained their integrity after repeated bendings. To investigate the radical-forming ability of the polyamides for decomposing surrounding harmful materials, degradation of methylene blue by the polymer films was studied.

Study of fluorinated poly(1,3,4-oxadiazole-amide)s

Three aromatic fluorinated poly(1,3,4-oxadiazole-amide) were synthesized by solution polycondensation reaction of aromatic diamines containing preformed 1,3,4-oxadiazole ring with a diacid chloride incorporating hexafluorisopropylidene unit. All polymers