84392-26-7

Basic information

• Product Name: 2-(4-T-BUTYLPHENYL) BENZOIC ACID
• Synonyms: 2-(4-T-BUTYLPHENYL) BENZOIC ACID;4'-(1,1-dimethylethyl)-[1,1'-Biphenyl]-2-carboxylic acid
• CAS NO: 84392-26-7
• Molecular Formula: C17H18 O2
• Molecular Weight: 254.32
• Mol File: 84392-26-7.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-T-BUTYLPHENYL) BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-T-BUTYLPHENYL) BENZOIC ACID(84392-26-7)
• EPA Substance Registry System: 2-(4-T-BUTYLPHENYL) BENZOIC ACID(84392-26-7)

Safety Data

• Hazardous Substances Data: 84392-26-7(Hazardous Substances Data)

Usage

Uses

2-(4-t-Butylphenyl)benzoic acid

Upstream product

• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 653589-95-8 2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)benzoic acid methyl ester 
• 1829-28-3 ethyl 2-iodobenzoate 
• 88-67-5 2-Iodobenzoic acid 
• 35779-04-5 1-tert-butyl-4-iodobenzene 
• 65-85-0 benzoic acid 
• 123324-71-0 p-tert-butylphenylboronic acid 
• 610-97-9 o-iodo-methyl-benzoic acid 
• 1528793-37-4 methyl 4′-(tert butyl)-[1,1′-biphenyl]-2-carboxylate 
• 863492-39-1 4'-tert-butylbiphenyl-2-carboxylic acid ethyl ester 

Relevant articles and documents

SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS

The application relates to substituted hydantoinamides of formula (I) as ADAMTS7 antagonists, to processes for their preparation, their use alone or in combination for the treatment or prophylaxis of diseases, in particular of cardiovascular diseases, including atherosclerosis, coronary artery disease (CAD), peripheral vascular disease (PAD), arterial occlusive disease or restenosis after angioplasty. R1 is hydrogen, alkyl, cycloalkyl, heterocycloalkyl, heteroaryl or phenyl; R2 is hydrogen, cyano, halogen, alkylsulfonyl, alkyl, cycloalkyl or alkoxy; R3, R4, R5, R6, R7 and R8 are independently hydrogen, halogen, alkyl or alkoxy; most groups being optionally substituted; with the proviso that at least one of R2, R3, R4 is H; X1, X2, X3, X4, X5 and X6 are independently N or C; with the proviso that in each ring maximal one X is N.

Facile preparation of 3,4-benzocoumarins from 2-arylbenzoic acids with NCS and NAI

– Treatment of 2-arylbenzoic acids with N-chlorosuccinimide (NCS) and NaI at 70 °C under fluorescent lighting condition gave the corresponding 3,4-benzocoumarins in good yields under transition-metal-free condition. It was found that the reactivity of NCS

Visible-Light-Induced Arene C(sp 2)-H Lactonization Promoted by DDQ and tert -Butyl Nitrite

A visible-light photocatalytic aerobic oxidative lactonization of arene C(sp 2)-H bonds proceeds in the presence of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and tert -butyl nitrite (TBN). Under the optimized conditions, a range of 2-arylbenzoic acids is converted into the corresponding benzocoumarin derivatives in moderate to excellent yields. This method is characterized by its atom economy, mild reaction conditions, the use of a green oxidant and metal-free catalysis.