53673-16-8

Basic information

• Product Name: N-(2-AMINOETHYL)-2-METHYLPROPANAMIDE
• Synonyms: N-(2-AMINOETHYL)-2-METHYLPROPANAMIDE;N-(2-aminoethyl)-2-methylpropanamide(SALTDATA: HCl);N-(2-Aminoethyl)-2-methylpropanamide HCl
• CAS NO: 53673-16-8
• Molecular Formula: C₆H₁₄N₂O
• Molecular Weight: 130.19
• Mol File: 53673-16-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-AMINOETHYL)-2-METHYLPROPANAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-AMINOETHYL)-2-METHYLPROPANAMIDE(53673-16-8)
• EPA Substance Registry System: N-(2-AMINOETHYL)-2-METHYLPROPANAMIDE(53673-16-8)

Safety Data

• Hazardous Substances Data: 53673-16-8(Hazardous Substances Data)

Upstream product

• 107-15-3 ethylenediamine 
• 547-63-7 Methyl isobutyrate 
• 79-31-2 isobutyric Acid 
• 97-62-1 Ethyl isobutyrate 

Downstream Products

• 56203-51-1 N-<2-(benzylamino)ethyl>isobutyramide 
• 66888-42-4 phenyl N-(β-isobutyramidoethyl)carbamate 
• 53672-46-1 N-{2-[2-Hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-ethyl}-isobutyramide 
• 53671-24-2 1-(2-methoxyphenoxy)-3-β-isobutyramidoethylamino-2-propanol 
• 121508-88-1 N-[2-(3-Benzyloxy-2-hydroxy-propylamino)-ethyl]-isobutyramide 
• 56203-07-7 2-(β-isobutyramido-ethyl)amino-1-p-bromophenylethanol 
• 56202-72-3 1-phenyl-2-(β-isobutyramidoethyl)amino-ethanol 
• 83029-57-6 N-(2-[2-hydroxy-3-phenoxypropyl]aminoethyl)-isobutyramide 
• 87484-92-2 Methyl 3-[4-[2-Hydroxy-3-[N-[2-(methylpropionamido)ethyl]amino]propoxy-]phenyl]propionate 
• 66824-97-3 1-(o-chlorophenoxy)-3-β-[3-(β-isobutyramidoethyl)ureido] ethylaminopropan-2-ol 
• 53672-71-2 N-<2-<<2-hydroxy-3-(3,4-dihydroxyphenoxy)propyl>amino>ethyl>-2-methylpropanamide 
• 53672-74-5 N-{2-[2-Hydroxy-3-(4-hydroxy-3-hydroxymethyl-phenoxy)-propylamino]-ethyl}-isobutyramide 
• 87721-48-0 3-[[2-(Isopropylcarbonylamino)]ethyl]amino-2-hydroxypropyl 2-Fluorobenzoate Hydrochloride 
• 56203-08-8 2-(β-isobutyramidoethyl)-amino-1-p-methoxyphenylethanol 

Relevant articles and documents

Colloid and nanosized catalysts in organic synthesis: XIII. Synthesis of 2-R-2-imidazolines catalyzed by copper and iron oxide nanoparticles

The reaction of carboxylic acids with ethylenediamine catalyzed by copper or iron oxide nanoparticles proceeds at 80°C with azeotropic water distilling off during 2-8 h to form 2-R-2-imidazolines. Acyl and diacyl derivatives of ethylenediamine are formed in the reaction as side products.

New Histidyl amino acid derivatives, and pharmaceutical composition comprising the same

A compound of the formula: STR1 wherein R1 is lower alkyl optionally substituted with a substituent selected from the group consisting of acyl, hydroxy, lower alkoxy, aryl, lower alkylthio and a group of the formula: STR2 in which R5 is hydrogen or acyl and R6 is hydrogen or lower alkyl; aryl; or amino optionally substituted with substituent(s) selected from the group consisting of lower alkyl and acyl; and R2 is hydrogen or lower alkyl; or R1 and R2 are taken together with the attached nitrogen atom to form a heterocyclic group optionally substituted with substituent(s) selected from the group consisting of lower alkyl, hydroxy(lower )alkyl, lower alkoxy(lower)alkyl, acyl(lower)alkyl, oxo and acyl; R3 is hydrogen or lower alkyl; and R4 is lower alkyl; and its pharmaceutically acceptable salt, processes for the preparation thereof and pharmaceutical composition comprising the same.