53881-34-8

Basic information

• Product Name: Benzoyl chloride, 2-(1-methylethyl)- (9CI)
• Synonyms: 2-isopropylbenzoyl chloride;Benzoyl chloride, 2-(1-methylethyl)- (9CI)
• CAS NO: 53881-34-8
• Molecular Formula: C₁₀H₁₁ClO
• Molecular Weight: 182.64674
• Product Categories: ACIDHALIDE
• Mol File: 53881-34-8.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzoyl chloride, 2-(1-methylethyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 2-(1-methylethyl)- (9CI)(53881-34-8)
• EPA Substance Registry System: Benzoyl chloride, 2-(1-methylethyl)- (9CI)(53881-34-8)

Safety Data

• Hazardous Substances Data: 53881-34-8(Hazardous Substances Data)

Upstream product

• 851199-82-1 2-isopropylphenyl trifluoromethanesulfonate 
• 88-69-7 2-(1-methylethyl)phenol 
• 7073-94-1 1-bromo-2-isopropylbenzene 
• 2438-04-2 2-isopropylbenzoic acid 

Downstream Products

• 22679-50-1 o,o'-diisopropylbenzophenone 
• 19103-09-4 (2-isopropylphenyl)(phenyl)methanone 
• 38524-08-2 3-Chloro-2-(2-isopropyl-benzoylamino)-propionic acid methyl ester 
• 19194-52-6 3,3-dimethylisoindolin-1-one 
• 89424-16-8 Ethyl-(2-isopropylbenzoyl)-acetat 
• 918867-78-4 N-(tert-butyl)-2-(prop-1-en-2-yl)benzamide 
• 1622869-27-5 C₂₄H₂₁F₃N₂O₃ 
• 1622869-14-0 C₂₄H₂₄N₂O₂ 
• 98766-83-7 (+/-)2-Isopropyl-benzhydrylchlorid 
• 21945-82-4 (2-isopropylphenyl)(phenyl)methanol 

Relevant articles and documents

N-Heterocyclic-Carbene-Catalyzed C–H Acylation via Radical Relay

A method of N-fluorocarboxamide-directed N-heterocyclic-carbene (NHC)-catalyzed benzylic C–H acylation with aldehydes via the hydrogen atom transfer strategy is disclosed. This transformation involves a sequence of single-electron transfer, 1,5-hydrogen a

Facile Synthesis of Alkylidene Phthalides by Rhodium-Catalyzed Domino C?H Acylation/Annulation of Benzamides with Aliphatic Carboxylic Acids

The Rh-catalyzed ortho-C(sp2)?H functionalization of 8-aminoquinoline-derived benzamides with aliphatic acyl fluorides generated in situ from the corresponding acids has been developed. This reaction initiated with 8-aminoquinoline-directed ortho-C(sp2)?H acylation, which was accompanied by subsequent intramolecular nucleophilic acyl substitution of amide group to produce alkylidene phthalides This approach exhibits high stereo-selectivity for Z-isomer products, and tolerates a variety of functional groups as well as aliphatic carboxylic acids with diverse structural scaffolds.

Synthesis of Lactams via Ir-Catalyzed C-H Amidation Involving Ir-Nitrene Intermediates

x-membered lactams were synthesized via either an amidation of sp3 C-H bonds or an electrophilic substitution of arenes via Ir-nitrene intermediates. With the employment of a readily available iridium catalyst in dichloromethane or hexafluoro-2-propanol, a wide range of lactams were synthesized in good to excellent yields with high selectivity.