14377-33-4

Basic information

• Product Name: Benzoyl chloride, 3,5-bis(1,1-dimethylethyl)-
• CAS NO: 14377-33-4
• Molecular Formula: C15H21ClO
• Molecular Weight: 252.784
• Mol File: 14377-33-4.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 3,5-bis(1,1-dimethylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 3,5-bis(1,1-dimethylethyl)-(14377-33-4)
• EPA Substance Registry System: Benzoyl chloride, 3,5-bis(1,1-dimethylethyl)-(14377-33-4)

Safety Data

• Hazardous Substances Data: 14377-33-4(Hazardous Substances Data)

Upstream product

• 16225-26-6 3,5-di-tert-butylbenzoic acid 
• 1756-31-6 1-(3,5-di-tert-butylphenyl)ethanone 
• 22385-77-9 1-bromo-3,5-di-tert-butylbenzene 

Downstream Products

• 1756-31-6 1-(3,5-di-tert-butylphenyl)ethanone 
• 14377-60-7 3,5-Di-tert.-butyl-benzoesaeure-<1,3-bis-diaethylamino-propyl-(2)-ester> 
• 14377-29-8 3,5-Di-tert.-butyl-benzoesaeure-<2-diaethylamino-aethylester> 
• 82505-19-9 3,5-Di-tert-butyl-thiobenzoesaeure 
• 389799-73-9 1,9-bis-(3,5-di-tert-butylbenzoyl)-5-mesityldipyrromethane 
• 389799-87-5 1,9-bis-(3,5-di-tert-butylbenzoyl)-5-{4-[2-(trimethylsilyl)ethynyl]phenyl}dipyrromethane 
• 378750-93-7 S-2-pyridyl 3,5-di-tert-butylbenzenecarbothioate 
• 497080-01-0 3,5-di-tert-butyl-N-(2-mercapto-ethyl)-benzamide 
• 878218-33-8 (3,5-di-tert-butylphenyl){5-[[4-(5,5-dimethyl-1,3-dioxan-2-yl)phenyl](1H-pyrrol-2-yl)methyl]-1H-pyrrol-2-yl}methanone 
• 878218-42-9 1,9-bis(3,5-di-tert-butylbenzoyl)-5-[4-(5,5-dimethyl-1,3-dioxan-2-yl)phenyl]dipyrromethane 
• 307930-84-3 1,9-bis(3,5-di-tert-butylbenzoyl)-5-(4-iodophenyl)dipyrromethane 
• 441793-61-9 C₃₇H₄₇NO₄ 
• 1004987-36-3 O-(3,5-di-t-butylbenzoyl)-N-tosyl-(L)-allo-threonine benzyl ester 
• 890415-81-3 C₂₃H₂₈N₂O₃ 

Relevant articles and documents

Dynamic covalent approach to [2]- and [3]rotaxanes by utilizing a reversible thiol-disulfide interchange reaction

A dynamic covalent approach to disulfide-containing [2]- and [3]rotaxanes is described. Symmetrical dumbbell-shaped compounds with two secondary ammonium centers and a central located disulfide bond were synthesized as components of rotaxanes. The rotaxan

Synthesis and antimicrobial activity of small cationic amphipathic aminobenzamide marine natural product mimics and evaluation of relevance against clinical isolates including ESBL–CARBA producing multi-resistant bacteria

A library of small aminobenzamide derivatives was synthesised to explore a cationic amphipathic motif found in marine natural antimicrobials. The most potent compound E23 displayed minimal inhibitory concentrations (MICs) of 0.5–2 μg/ml against several Gr

Facile route to an all-organic, triply threaded, interlocked structure by templated dynamic clipping

[2]Rotaxanes are a class of mechanically interlocked molecules which are generally depicted by an "axle-in-wheel" model, in which a dumbbell-shaped linear component is threaded through a macrocyclic component (Scheme 1 a). Functionalization of the rotaxan