3936-54-7

Basic information

• Product Name: ethyl propionate
• Synonyms: ethyl propionate
• CAS NO: 3936-54-7
• Molecular Weight: 221.299
• Mol File: 3936-54-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: ethyl propionate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl propionate(3936-54-7)
• EPA Substance Registry System: ethyl propionate(3936-54-7)

Safety Data

• Hazardous Substances Data: 3936-54-7(Hazardous Substances Data)

Upstream product

• 539-74-2 Ethyl 3-bromopropionate 
• 64-04-0 phenethylamine 
• 140-88-5 ethyl acrylate 
• 4244-84-2 ethyl β-alaninate hydrochloride 
• 103-63-9 1-phenyl-2-bromoethane 

Downstream Products

• 57958-47-1 3,3'-phenethylimino-di-propionic acid diethyl ester 
• 157737-84-3 N-(2-Phenylethyl)-N-(2-carbethoxyethyl)-4-aminobuttersaeureethylester 
• 150871-33-3 ethyl N--DL-α-methyltryptophanyl>-N-(2-phenylethyl)-3-aminopropionate 
• 667458-85-7 3-[(2-Benzenesulfonyl-acetyl)-phenethyl-amino]-propionic acid ethyl ester 
• 371229-33-3 3-[(2-Benzenesulfonyl-2-diazo-acetyl)-phenethyl-amino]-propionic acid ethyl ester 
• 892863-29-5 3-(Phenethyl-phenylacetyl-amino)-propionic acid ethyl ester 
• 4661-35-2 ethyl 4-hydroxy-5-oxo-1-phenethyl-2,5-dihydro-1H-pyrrole-3-carboxylate 
• 892863-34-2 3-{[2-(4-Methyl-pyridin-2-yl)-acetyl]-phenethyl-amino}-propionic acid ethyl ester 
• 1240347-89-0 (6Z,9Z,12Z,15Z)-1-[(2-phenylethyl)amino]octadeca-6,9,12,15-tetraen-3-one 
• 1274874-85-9 tert-butyl ((6Z,9Z,12Z,15Z)-3-hydroxyoctadeca-6,9,12,15-tetraen-1-yl)(phenethyl)carbamate 
• 1274874-86-0 tert-butyl ((6Z,9Z,12Z,15Z)-3-oxooctadeca-6,9,12,15-tetraen-1-yl)(phenethyl)carbamate 
• 1274874-84-8 tert-butyl (3-hydroxypropyl)(phenethyl)carbamate 
• 1274874-79-1 tert-butyl (3-oxopropyl)(phenethyl)carbamate 

Relevant articles and documents

EIF4E INHIBITORS AND USES THEREOF

The present invention provides compounds inhibiting elF4E activity and compositions and methods of using thereof.

Promiscuous behavior of Rhizomucor miehei lipase in the synthesis of N-substituted β-amino esters

A mild and efficient procedure for the aza-Michael addition of amines to acrylates by using lipases as catalysts is reported. Various lipases, mono- and bifunctional amines, alkyl acrylates, and reaction parameters were studied. Under the optimal conditio

Aurora kinase A inhibitors: Identification, SAR exploration and molecular modeling of 6,7-dihydro-4H-pyrazolo-[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8-dione scaffold

Tricyclic 6,7-dihydro-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8-dione was identified as a novel scaffold for Aurora kinase A inhibition through virtual screening. SAR exploration coupled with molecular modeling of 8a reveals the minimum pharmacophore requirements for Aurora kinase A inhibition.