111153-16-3

Basic information

• Product Name: 4'-(BENZYLOXY)[1,1'-BIPHENYL]-4-CARBOXYLIC ACID
• Synonyms: 4'-(BENZYLOXY)[1,1'-BIPHENYL]-4-CARBOXYLIC ACID;AKOS BAR-0999
• CAS NO: 111153-16-3
• Molecular Formula: C₂₀H₁₆O₃
• Molecular Weight: 304.34
• Mol File: 111153-16-3.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4'-(BENZYLOXY)[1,1'-BIPHENYL]-4-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-(BENZYLOXY)[1,1'-BIPHENYL]-4-CARBOXYLIC ACID(111153-16-3)
• EPA Substance Registry System: 4'-(BENZYLOXY)[1,1'-BIPHENYL]-4-CARBOXYLIC ACID(111153-16-3)

Safety Data

• Hazardous Substances Data: 111153-16-3(Hazardous Substances Data)

Usage

Uses

4-(4-Benzyloxyphenyl)benzoic Acid is used as a reactant in the synthesis of HDAC inhibitors.

Upstream product

• 40501-41-5 methyl 4'-hydroxy-4-biphenylcarboxylate 
• 58574-03-1 4'-Hydroxybiphenyl-4-carboxylic acid 
• 50670-76-3 ethyl 4-hydroxy-4-biphenyl carboxylate 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 
• 85683-74-5 benzynyl bromide 
• 68-12-2 N,N-dimethyl-formamide 
• 141285-38-3 benzyl 4'-(benzyloxy)biphenyl-4-carboxylate 

Downstream Products

• 1263269-29-9 2-ethylbutyl 4'-(benzyloxy)biphenyl-4-carboxylate 
• 75472-37-6 4'-benzyloxy-4-biphenylcarboxaldehyde 
• 111153-17-4 4-benzyloxy-biphenyl-4'-carboxylic acid chloride 
• 128055-22-1 4'-(6-Acryloyloxy-hexyloxy)-biphenyl-4-carboxylic acid 4-((S)-1-difluoromethyl-heptyloxycarbonyl)-phenyl ester 
• 128055-21-0 4'-(6-Acryloyloxy-hexyloxy)-biphenyl-4-carboxylic acid 4-((R)-1-difluoromethyl-heptyloxycarbonyl)-phenyl ester 
• 128083-47-6 (R)-(+)-4-<<<1-(trifluoromethyl)decyl>oxy>carbonyl>phenyl 4'-(benzyloxy)biphenyl-4-carboxylate 
• 128054-87-5 (S)-(-)-4-<<<1-(trifluoromethyl)decyl>oxy>carbonyl>phenyl 4'-(benzyloxy)biphenyl-4-carboxylate 
• 128055-05-0 4'-(8-Acryloyloxy-octyloxy)-biphenyl-4-carboxylic acid 4-((R)-1-trifluoromethyl-heptyloxycarbonyl)-phenyl ester 
• 128055-06-1 4'-(8-Acryloyloxy-octyloxy)-biphenyl-4-carboxylic acid 4-((S)-1-trifluoromethyl-heptyloxycarbonyl)-phenyl ester 
• 128055-12-9 4'-(2-Acryloyloxy-ethoxy)-biphenyl-4-carboxylic acid 4-((R)-1-pentafluoroethyl-heptyloxycarbonyl)-phenyl ester 
• 128055-13-0 4'-(2-Acryloyloxy-ethoxy)-biphenyl-4-carboxylic acid 4-((S)-1-pentafluoroethyl-heptyloxycarbonyl)-phenyl ester 
• 128055-03-8 4'-(6-Acryloyloxy-hexyloxy)-biphenyl-4-carboxylic acid 4-((R)-1-trifluoromethyl-heptyloxycarbonyl)-phenyl ester 
• 128055-04-9 4'-(6-Acryloyloxy-hexyloxy)-biphenyl-4-carboxylic acid 4-((S)-1-trifluoromethyl-heptyloxycarbonyl)-phenyl ester 
• 128054-90-0 (R)-(+)-4-<<<1-(pentafluoroethyl)heptyl>oxy>carbonyl>phenyl 4'-(benzyloxy)biphenyl-4-carboxylate 

Relevant articles and documents

Regioselective Hydroformylation of Internal and Terminal Alkenes via Remote Supramolecular Control

Regioselective catalytic transformations using supramolecular directing groups are increasingly popular as it allows for control over challenging reactions that may otherwise be impossible. In most examples the reactive group and the directing group are close to each other and/or the linker between the directing group is very rigid. Achieving control over the regioselectivity using a remote directing group with a flexible linker is significantly more challenging due to the large conformational freedom of such substrates. Herein, we report the redesign of a supramolecular Rh–bisphosphite hydroformylation catalyst containing a neutral carboxylate receptor (DIM pocket) with a larger distance between the phosphite metal binding moieties and the DIM pocket. For the first time regioselective conversion of internal and terminal alkenes containing a remote carboxylate directing group is demonstrated. For carboxylate substrates that possess an internal double bond at the Δ-9 position regioselectivity is observed. As such, the catalyst was used to hydroformylate natural monounsaturated fatty acids (MUFAs) in a regioselective fashion, forming of an excess of the 10-formyl product (10-formyl/9-formyl product ratio of 2.51), which is the first report of a regioselective hydroformylation reaction of such substrates.

SUBSTITUTED (AMINOIMINOMETHYL OR AMINOMETHYL) BENZOHETEROARYL COMPOUNDS

This invention is directed to an (aminoiminomethyl or aminomethyl) benzoheteroaryl compound of formula I which is useful for inhibiting the activity of Factor Xa by combining said compound with a composition containing Factor Xa. The present invention is also directed to compositions containing compounds of the formula I, methods for their preparation, their use, such as in inhibiting the formation of thrombin or for treating a patient suffering from, or subject to, a disease state associated with a physiologically detrimental excess amount of thrombin.

Tetralin compound, liquid crystal material and liquid crystal composition

The invention to provide novel tetralin compounds, liquid crystal materials and liquid crystal compositions, which can constitute a liquid crystal element affording a wide operating temperature range, a high switching speed and a small consumption of elec