30039-44-2

Basic information

• Product Name: (4-nitrophenyl)methyl propanoate
• Synonyms: (4-nitrophenyl)methyl propanoate
• CAS NO: 30039-44-2
• Molecular Formula: C₁₀H₁₁NO₄
• Molecular Weight: 0
• Mol File: 30039-44-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 318.9°Cat760mmHg
• Flash Point: 141.9°C
• Appearance: /
• Density: 1.226g/cm³
• Vapor Pressure: 0.00035mmHg at 25°C
• Refractive Index: 1.538
• CAS DataBase Reference: (4-nitrophenyl)methyl propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (4-nitrophenyl)methyl propanoate(30039-44-2)
• EPA Substance Registry System: (4-nitrophenyl)methyl propanoate(30039-44-2)

Safety Data

• Hazardous Substances Data: 30039-44-2(Hazardous Substances Data)

Usage

Description

(4-nitrophenyl)methyl propanoate is a chemical compound that consists of a nitrophenyl group attached to a methyl propanoate group. It is a yellow crystalline solid with high reactivity due to the presence of the nitro group. (4-nitrophenyl)methyl propanoate is used in organic synthesis and as a pharmaceutical intermediate.

Uses

Used in Organic Synthesis:
(4-nitrophenyl)methyl propanoate is used as a building block in the synthesis of various organic compounds. Its reactivity and the presence of the nitrophenyl group make it a versatile component in the creation of new molecules.
Used in Pharmaceutical Industry:
(4-nitrophenyl)methyl propanoate is used as a pharmaceutical intermediate, playing a crucial role in the development of new drugs. Its unique structure and reactivity contribute to the synthesis of pharmaceutical compounds with potential therapeutic applications.
Used in Nitroaromatic Compounds:
(4-nitrophenyl)methyl propanoate is used as a nitroaromatic compound in various applications. The nitrophenyl group provides specific properties that are valuable in different chemical processes and reactions.
It is important to handle (4-nitrophenyl)methyl propanoate with caution due to its potential hazards, as it is a reactive chemical compound.

InChI:InChI=1/C10H11NO4/c1-2-10(12)15-7-8-3-5-9(6-4-8)11(13)14/h3-6H,2,7H2,1H3

Upstream product

• 619-73-8 4-nitrobenzyl chloride 
• 72-03-7 propanoate 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 802294-64-0 propionic acid 

Relevant articles and documents

Facile construction of thermo-responsive Pickering emulsion for esterification reaction in phase transfer catalysis system

In this paper, a thermo-responsive Pickering emulsion (PE) is constructed for the esterification reaction in the phase transfer catalysis (PTC) system. Silica nanoparticle modified by alkyl polyoxyethylene ether and tetrabutylammonium bromide (TBAB) is the highly efficient thermo-responsive Pickering emulsifier to stabilize the diisopropyl ketone-in-water emulsion. PEs can keep stable at room temperature for 3 days and demulsify only in the condition of elevated temperature and agitation, which causes the easy product separation and aqueous phase recycling. The adsorption of TBA+ and nonionic surfactant via electrostatic interaction and hydrogen bonding, respectively, can increase the hydrophobicity and the emulsifying capacity of silica nanoparticle. The ion-pair of TBA+ and reactant anion is generated and can be transferred into the organic phase, initiating the bond-forming reaction. The modifying effect of polyoxyethylene ether is weakened with the increase of temperature due to the loss of the hydrogen bonding interaction, resulting in the demulsification of PEs. Moreover, the cloud point of polyoxyethylene ether is the temperature for the complete separation of two phases. In this PTC system, the conversion rate for the esterification can reach to 92 % and the aqueous phase can be reused at least 5 times without sacrifice of the catalytic activity, demonstrating the potential application in industry.

Sodium Borohydride-Carboxylic Acid Systems - A new Method of Acylation of Alcohols, Phenols and Thiophenols

A new method of acylation of alcohols, phenols and thiophenols in sodium borohydride-carboxylic acid system is described.A plausible mechanism of this acylation through tetraacyloxyborate derivative has been postulated.