88038-94-2

Usage

Chemical Properties

Pale yellow solid

Upstream product

• 588-93-2 p-bromo-n-propylbenzene 
• 58743-76-3 4-cyano-4'-n-propylbiphenyl 
• 58743-81-0 4-n-propyl-4'-bromobiphenyl 

Downstream Products

• 1392007-24-7 4-(4-n-propylphenyl)benzoic acid 4-cyano-3,5-difluorophenyl ester 
• 469859-70-9 1-tert-butyl 4-(4-n-propylphenyl)benzoate 
• 1027281-62-4 (R)-2-(4'-Propyl-biphenyl-4-yl)-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 
• 1027426-91-0 (R)-3-Hydroxy-2-[(4'-propyl-biphenyl-4-carbonyl)-amino]-propionic acid methyl ester 
• 65195-14-4 4'-propyl[1,1'-biphenyl]-4-carboxylic acid chloride 

Relevant academic research and scientific papers

Optically active compound and photosensitive resin composition

A photoactive compound is used in combination with a photosensitizer, represented by the following formula (1): A?[(J)m?(X-Pro)]n ??(1) wherein A represents a hydrophobic unit comprising at least one kind of hydrophobic groups selected from a hydrocarbon group and a heterocyclic group, J represents a connecting group, X-Pro represents a hydrophilic group protected by a protective group Pro which is removable by light exposure, m represents 0 or 1, and n represents an integer of not less than 1. The protective group Pro may be removable by light exposure in association with the photosensitizer (especially, a photo acid generator), or may be a hydrophobic protective group. The hydrophilic group may be a hydroxyl group or a carboxyl group. The photoactive compound has high sensitivity to a light source of short wavelength beams, for resist application, therefore, the photoactive compound is advantageously used for forming a pattern with high resolution.

N-acylsulfonamide apoptosis promoters

N-Benzoyl arylsulfonamides having the formula are BCL-Xl inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-Xl inhibiting compositions and methods of promoting apoptosis in a mammal.

N-Acylsulfonamide apoptosis promoters

N-Benzoyl arylsulfonamides having the formula Are BCL-X1 inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-X1 inhibiting compositions and methods of promoting apoptosis in a mammal.

Synthesis and magnetic properties of some crystalline nitroxide radicals

The syntheses of different nitroxide radicals are reported. The thermal behaviour of the nitroxide radicals was examined by polarizing microscopy, differential scanning calorimetry as well as X-ray diffraction experiments. Temperature dependent magnetic susceptibility measurements were carried out in order to determine the magnetic properties of these nitroxide radicals. The majority of the radicals presented here show weak antiferromagnetic exchange interactions.

Cyano-substituted biphenyl compounds and liquid crystalline dielectrics containing the same

Biphenyl derivatives of the formula: STR1 wherein X is --CO--O-- or --O--CO--, R1 and R4 are alkyl of 1 to 10 carbon atoms, and one of R2 and R3 is CN and the other is H, are useful for lowering the dielectric anisotropy of liquid crystalline dielectrics.

Biphenyl esters and liquid crystalline mixtures comprising them

Biphenyl esters of the formula STR1 wherein X is --CO--O-- or --O--CO-- and R1 and R2 each are alkyl or alkoxy of 1 - 8 carbon atoms, enlarge significantly the temperature range of the nematic phase of liquid-crystalline compositions without adversely affecting other properties.