7063-21-0

Basic information

• Product Name: SodiuM 3-oxo-3-phenylpropanoate
• Synonyms: SodiuM 3-oxo-3-phenylpropanoate
• CAS NO: 7063-21-0
• Molecular Formula: C₉H₇O₃*Na
• Molecular Weight: 186.13985
• Mol File: 7063-21-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 517.1°C at 760 mmHg
• Flash Point: 266.5°C
• Appearance: /
• Density: 1.25g/cm³
• Vapor Pressure: 8.47E-11mmHg at 25°C
• Refractive Index: 1.63
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: SodiuM 3-oxo-3-phenylpropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: SodiuM 3-oxo-3-phenylpropanoate(7063-21-0)
• EPA Substance Registry System: SodiuM 3-oxo-3-phenylpropanoate(7063-21-0)

Safety Data

• Hazardous Substances Data: 7063-21-0(Hazardous Substances Data)

Usage

General Description

Sodium 3-oxo-3-phenylpropanoate is a chemical compound with the molecular formula C9H7NaO3. It is a white crystalline powder that is soluble in water. SodiuM 3-oxo-3-phenylpropanoate is commonly used in the pharmaceutical industry as a pharmaceutical intermediate and as a precursor in the synthesis of various pharmaceutical products. It can also be used as a food additive and flavoring agent. However, it is important to handle this chemical with caution, as it can be a skin and eye irritant and may cause respiratory irritation if inhaled.

InChI:InChI=1/C26H37N5O2S2/c1-6-9-10-19(7-2)17-31-25(33)22(35-26(31)34)15-20-18(4)21(16-27)24(32)28(5)23(20)30-13-11-29(8-3)12-14-30/h15,19H,6-14,17H2,1-5H3

Upstream product

• 98-86-2 acetophenone 
• 536755-29-0 N,N'-dimethylimidazolium-2-carboxylate 
• 671779-18-3 N-methyl-N'-n-butylimidazolium-2-carboxylate 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 143-66-8 sodium tetraphenyl borate 
• 917604-39-8 1,3-bis(2,6-diisopropylphenyl)imidazolylium-2-carboxylate 

Downstream Products

• 23310-52-3 1-methyl-1,3-dihydro-2,1-benzisothiazol-3-thion 
• 81698-09-1 1-methyl-3-phenacylidene-2,1-benzisothiazole 
• 81698-10-4 1-Phenyl-2-[1-phenyl-1H-benzo[c]isothiazol-(3Z)-ylidene]-ethanone 
• 81698-11-5 methyl 2-phenylaminodithiobenzoate 
• 111865-10-2 1-methyl-2,1-benzisothiazole<2,3-b>-5-phenyl-1,2-dithiole 
• 614-20-0 3-oxo-3-phenylpropionic acid 

Relevant articles and documents

Asymmetric Mannich synthesis of α-amino esters by anion-binding catalysis

We report a scalable, one-pot Mannich route to enantioenriched α-amino esters by direct reaction of α-chloroglycine ester as a practical imino ester surrogate. The reaction is promoted by a chiral aminothiourea, which is proposed to operate cooperatively

A PRODRUG COMPRISING BETA-KETO CARBOXYLIC ACID, BETA-KETO CARBOXYLIC ACID SALT OR BETA-KETO CARBOXYLIC ACID ESTER FOR DRUG DELIVERY

There is provided a prodrug of a pharmaceutically active agent, said prodrug comprising a beta-keto carboxylic acid, a beta-keto carboxylic acid salt or a beta-keto carboxylic acid ester functional group, to a pharmaceutical composition comprising the prodrug, and to the use of the prodrug or composition for treatment of a mammalian subject suffering from a condition which can be cured or alleviated by administration of said pharmaceutically active agent. There is further provided a method of inhibiting decarboxylation of a compound comprising a beta-keto carboxylic acid or a salt thereof with a monovalent cation, characterized in that a dry salt of said beta-keto carboxylic acid with a divalent or polyvalent cation is prepared.