22573-54-2

Basic information

• Product Name: (R)-3-phenyl-4-methylpentanoic acid
• Synonyms: (R)-3-phenyl-4-methylpentanoic acid
• CAS NO: 22573-54-2
• Molecular Weight: 192.258
• Mol File: 22573-54-2.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: (R)-3-phenyl-4-methylpentanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-phenyl-4-methylpentanoic acid(22573-54-2)
• EPA Substance Registry System: (R)-3-phenyl-4-methylpentanoic acid(22573-54-2)

Safety Data

• Hazardous Substances Data: 22573-54-2(Hazardous Substances Data)

Upstream product

• 75-30-9 2-iodo-propane 
• 37612-74-1 (E)‐1‐(3,5‐dimethyl‐1H‐pyrazol‐1‐yl)‐3‐phenylprop‐2‐en‐1‐one 
• 621-82-9 Cinnamic acid 
• 126275-15-8 4-methyl-3-phenylpentanoyl chloride 
• 72277-17-9 (+/-)-ethyl 4-methyl-3-phenylpentanoate 
• 51690-50-7 4-methyl-3-phenylpentanoic acid 
• 1015083-84-7 C₁₇H₁₉NO 
• 13491-13-9 (R)-2-isopropyl-2-phenylacetic acid 
• 100-58-3 phenylmagnesium bromide 
• 102-92-1 Cinnamoyl chloride 
• 857637-83-3 (E)-(4S,5R)-4-benzyl-3-(3'-phenyl-2'-propenoyl)-5-(1'H,1'H,2'H,2'H-perfluorooctyl)-2-oxazolidinone 
• 63677-96-3 (E)-2-hydroxy-2-methyl-5-phenylpent-4-en-3-one 
• 857637-86-6 (3'R,4S,5R)-4-benzyl-3-(4'-methyl-3'-phenyl-pentanoyl)-5-(1'H,1'H,2'H,2'H-perfluorooctyl)-2-oxazolidinone 
• 155779-31-0 (4R,5S)-1,5-Dimethyl-3-((R)-4-methyl-3-phenyl-pentanoyl)-4-phenyl-imidazolidin-2-one 

Downstream Products

• 1462940-79-9 (S)-2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl 4-methyl-3-phenylpentanoate 
• 1462940-81-3 (S)-2,3,5,6-tetrafluoro-4-methylbenzyl 4-methyl-3-phenylpentanoate 
• 1462940-80-2 (R)-2,3,5,6-tetrafluoro-4-methylbenzyl 4-methyl-3-phenylpentanoate 
• 1462940-74-4 (R)-2,3,5,6-tetrafluoro-4-(methoxymethyl)benzyl 4-methyl-3-phenylpentanoate 

Relevant articles and documents

Identification of an Esterase Isolated Using Metagenomic Technology which Displays an Unusual Substrate Scope and its Characterisation as an Enantioselective Biocatalyst

Evaluation of an esterase annotated as 26D isolated from a marine metagenomic library is described. Esterase 26D was found to have a unique substrate scope, including synthetic transformations which could not be readily effected in a synthetically useful manner using commercially available enzymes. Esterase 26D was more selective towards substrates which had larger, more sterically demanding substituents (i. e. iso-propyl or tert-butyl groups) on the β-carbon, which is in contrast to previously tested commercially available enzymes which displayed a preference for substrates with sterically less demanding substituents (e.g. methyl group) at the β-carbon. (Figure presented.).

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.

Chiral Lewis acid catalyzed enantioselective conjugate radical additions to α,β-unsaturated 2-pyridyl ketones

We have investigated the utility of a pyridine-based achiral template in enantioselective conjugate radical additions. Georg Thieme Verlag Stuttgart.