802294-64-0

Basic information

• Product Name: propionic acid
• Synonyms: propionic acid
• CAS NO: 802294-64-0
• Molecular Weight: 74.0794
• Mol File: 802294-64-0.mol
• Article Data: 559

Chemical Properties

• CAS DataBase Reference: propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: propionic acid(802294-64-0)
• EPA Substance Registry System: propionic acid(802294-64-0)

Safety Data

• Hazardous Substances Data: 802294-64-0(Hazardous Substances Data)

Upstream product

• 56-23-5 tetrachloromethane 
• 79-21-0 peracetic acid 
• 928-49-4 hex-3-yne 
• 74-96-4 ethyl bromide 
• 15719-64-9 methylammonium carbonate 
• 141-52-6 sodium ethanolate 
• 187737-37-7 propene 
• 4437-51-8 3,4-hexanedione 
• 74-98-6 propane 
• 67-66-3 chloroform 
• 2548-85-8 (4E,8E,12E,15E,19E)-Docosa-4,8,12,15,19-pentaenoic acid 
• 646-07-1 4-Methylpentanoic acid 
• 111-14-8 oenanthic acid 
• 20487-40-5 tert-butyl propionate 

Downstream Products

• 637-65-0 tetrahydrofurfuryl propionate 
• 3194-15-8 2-propionylfuran 
• 100-71-0 2-Ethylpyridine 
• 536-75-4 4-Ethylpyridine 
• 5451-18-3 propionic acid-(3-tetrahydro[2]furyl-propyl ester) 
• 1122-69-6 2-ethyl-6-methylpyridine 
• 536-88-9 4-ethyl-2-methyl-pyridine 
• 13756-18-8 (R,S)-1-phenylethane-1,2-diol dipropionate 
• 324742-96-3 1-(4-methyl-thiazol-5-yl)-2-propionyloxy-ethane 
• 5453-26-9 3,6,9-tris-propionyloxy-1-tetrahydro[2]furyl-nonane 
• 101894-28-4 2,5-diphenyl-2-propionyloxy-furan-3-one 
• 61318-34-1 propionic acid-(2-phthalimido-ethyl ester) 
• 18503-88-3 3-(4-bromo-phenyl)-4-methyl-furazan 2-oxide 
• 56138-27-3 2-isopropyl-1,4-diphenyl-but-2c-ene-1,4-dione 

Relevant articles and documents

ON-LINE GC-IR IDENTIFICATION OF THE PRODUCTS OF HEXADECANE OXIDATION

The GC-IR investigation of the oxidation products of hexadecane indicated that the main components of the reaction mixture are carboxylic acids, ketones and gamma-lactones.The ir spectra of GC-effluents allow primarly the type of compounds to be determine

Cu(II)-Based Ionic Liquid Supported on SBA-15 Nanoparticles Catalyst for the Oxidation of Various Alcohols into Carboxylic Acids in the Presence of CO2

In this paper, we have produced carboxylic acids by the oxidation of various alcohols in the presence of CO2 using SBA-15/IL supported Cu(II) (SBA-15/IL/Cu(II)) as nanocatalyst. The obtained products showed to have excellent yields by taking into account of SBA-15/IL/Cu(II) nanocatalyst. In addition, the analysis of EDX, SEM, TGA, TEM, XPS, and FT-IR showed the heterogeneous structure of SBA-15/IL/Cu (II) catalyst. It is determined that, after using SBA-15 excess, the catalytic stability of the system was enhanced. Moreover, hot filtration provided a full vision in the heterogeneous catalyst nature. The recycling as well as reuse of the catalyst were studied in cases of coupling reactions many times. Moreover, we have studied the mechanism of the coupling reactions. Graphic Abstract: [Figure not available: see fulltext.]

An efficient and ultrastable single-Rh-site catalyst on a porous organic polymer for heterogeneous hydrocarboxylation of olefins

A heterogeneous hydrocarboxylation process of olefins to obtain carboxylic acids with one more carbon was first realized using a single-Rh-site catalyst formed on porous organic polymer (Rh1/POPs). The in situ formation of hydrophilic porous ionic polymer from hydrophobic POPs with the help of CH3I led to high activity and superb stability.