6995-48-8

Basic information

• Product Name: Benzenebutanoic acid, b-phenyl-, (R)-
• CAS NO: 6995-48-8
• Molecular Formula: C16H16O2
• Molecular Weight: 240.302
• Mol File: 6995-48-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzenebutanoic acid, b-phenyl-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenebutanoic acid, b-phenyl-, (R)-(6995-48-8)
• EPA Substance Registry System: Benzenebutanoic acid, b-phenyl-, (R)-(6995-48-8)

Safety Data

• Hazardous Substances Data: 6995-48-8(Hazardous Substances Data)

Upstream product

• 96706-62-6 3,4-diphenyl-butyric acid sec-butyl ester 
• 4374-49-6 3-benzyl-3-phenylpropionic acid 
• 98-80-6 phenylboronic acid 
• 949116-77-2 C₂₆H₃₁NO₃S 
• 147666-43-1 (R)-N-methyl-3,4-diphenylbutanamide 
• 100-52-7 benzaldehyde 
• 940-43-2 N-methyl-3-phenylpropanamide 
• 200803-34-5 (R)-3,4-Diphenyl-N-((S)-1-phenyl-ethyl)-butyramide 
• 200803-30-1 N-(3-phenylpropanoyl)-(S)-1-phenylethylamine 
• 100-39-0 benzyl bromide 
• 200803-59-4 (R)-3,4-Diphenyl-butyric acid butyl ester 
• 147666-56-6 ((R)-3,4-Diphenyl-butyryl)-methyl-carbamic acid tert-butyl ester 
• 127393-09-3 (2Z,4R)-2--4,5-diphenyl-2-pentenenitrile 
• 1589-82-8 phenylmagnesium bromide 

Downstream Products

• 1462940-63-1 (R)-2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl-3,4-diphenylbutanoate 

Relevant articles and documents

Palladium-Catalyzed Enantioselective Redox-Relay Heck Arylation of 1,1-Disubstituted Homoallylic Alcohols

An enantioselective redox-relay oxidative Heck arylation of 1,1-disubstituted alkenes to construct β-stereocenters was developed using a new pyridyl-oxazoline ligand. Various 1,2-diaryl carbonyl compounds were readily obtained in moderate yield and good to excellent enantioselectivity. Additionally, analysis of the reaction outcomes using multidimensional correlations revealed that enantioselectivity is tied to specific electronic features of the 1,1-disubstituted alkenol and the extent of polarizability of the ligand.

Asymmetric syntheses and bio-evaluation of novel chiral esters derived from substituted tetrafluorobenzyl alcohol

A series of novel chiral esters derived from tetrafluorobenzyl alcohol were designed and prepared via asymmetric synthesis. The target molecules have been identified on the basis of analytical spectra data. All newly synthesized compounds have been screened their potential insecticidal activity against Plutella xylostella compared with those of fenvalerate and d-trans-phenothrin by standard method, and the respective pairs of enantiomers (3-B1-R/S, 3-C1-R/S, 3-D1-R/S) indicated significantly different activities.

Synthese Asymetrique. 1. Additions Conjuguees Enantioselectives de Reactifs de Grignard a des Cinnamamides derivant du N-Methyl, N-Butyl et N-Benzyl (R)-(-)-2-Aminobutan-1-ol

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