87252-81-1

Usage

Uses

Used in Metal Plating Industry:
3-Benzoyl propionic acid oxime is used as a chelating agent for improving the adhesion of metal plating to the substrate, enhancing the quality and durability of the plated surface.
Used in Rubber and Plastics Production:
In the rubber and plastics industry, 3-benzoyl propionic acid oxime serves as a stabilizer, contributing to the production of higher quality materials with improved properties.
Used in Pesticide Formulation:
3-Benzoyl propionic acid oxime is utilized as a component in the formulation of pesticides, where its chelating properties can enhance the effectiveness and stability of the product.
Used in Water Treatment:
Due to its ability to bind with metal ions, 3-benzoyl propionic acid oxime is used in water treatment processes to improve water quality and remove unwanted metal contaminants.
Used as a Corrosion Inhibitor:
3-Benzoyl propionic acid oxime is employed as a corrosion inhibitor, helping to protect metal surfaces from degradation and prolonging their lifespan in various applications.

InChI:InChI=1/C10H11NO3/c12-10(13)7-6-9(11-14)8-4-2-1-3-5-8/h1-5,14H,6-7H2,(H,12,13)/b11-9+

Upstream product

• 2051-95-8 succinylbenzene 

Downstream Products

• 60769-68-8 1-hydroxy-5-phenyl-pyrrolidin-2-one 
• 2051-95-8 succinylbenzene 
• 201863-97-0 (S)-4-amino-4-phenylbutanoic acid 
• 201863-97-0 (R)-4-amino-4-phenylbutanoic acid 
• 1011-60-5 (rac)-4-amino-4-phenylbutanoic acid 
• 22050-10-8 (+/-)-5-phenyl-2-pyrrolidinone 
• 87253-03-0 4-Amino-4-phenyl-butyric acid octyl ester; hydrochloride 
• 87253-02-9 4-Amino-4-phenyl-butyric acid hexyl ester; hydrochloride 

Relevant academic research and scientific papers

Approach to Fully Substituted Cyclic Nitrones from N-Hydroxylactam Derivatives: Development and Application to the Total Synthesis of Cylindricine C

An approach to cyclic nitrones from N-hydroxylactam derivatives is documented. The nucleophilic addition of an organolithium reagent to an N-OSEM [SEM=2-(trimethylsilyl)ethoxymethyl] lactam forms a five-membered chelated intermediate, which undergoes both elimination and deprotection to give a fully substituted nitrone in a one-pot process. When combined with the N-oxidation of easily available chiral lactams, this method becomes especially useful for the quick synthesis of chiral nitrones in enantio-pure form, enabling the concise total synthesis of cylindricine C.

Enzymatic synthesis of chiral γ-amino acids using ω-transaminase

In this study, we successfully synthesized enantiomerically pure (R)- and (S)-γ-amino acids (>99% ee) using ω-transaminase (ω-TA) through kinetic resolution and asymmetric synthesis respectively. The present study demonstrates the high potentiality of ω-TA reaction for the production of chiral γ-amino acids.

FACTOR XA INHIBITORS

Compounds of formula (I) in which R1, n, Z, R3 and R4 have any of the meanings given in the specification, are inhibitors of the serine protease Factor Xa and are useful in the treatment of thrombotic disorders.

Structures of 4-Hydroxyimino-4-phenylbutanoic Acid, C10H11NO3 (I), and 5-Hydroxyimino-5-phenylpentanoic Acid, C11H13NO3 (II), at 223 K

Infinite polar chains of molecules with strong intermolecular hydrogen bonds (O-H...N and O-H...O) are observed between carboxyl and oxime groups N...O 2.697(1) and O...O 2.784(1) Angstroem for (I), and 2.690(2) and 2.744(2) Angstroem for (II), respectiv