93489-14-6

Basic information

• Product Name: 3-METHOXY-4-ETHOXYBENZYLAMINE
• Synonyms: 3-METHOXY-4-ETHOXYBENZYLAMINE;AKOS BC-2644;(4-Ethoxy-3-methoxybenzyl)amine;(4-ethoxy-3-methoxyphenyl)methanamine
• CAS NO: 93489-14-6
• Molecular Formula: C₁₀H₁₅NO₂
• Molecular Weight: 181.23
• Mol File: 93489-14-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 48 °C
• Boiling Point: 279.8±25.0 °C(Predicted)
• Appearance: /
• Density: 1.041±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 9.30±0.10(Predicted)
• CAS DataBase Reference: 3-METHOXY-4-ETHOXYBENZYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-METHOXY-4-ETHOXYBENZYLAMINE(93489-14-6)
• EPA Substance Registry System: 3-METHOXY-4-ETHOXYBENZYLAMINE(93489-14-6)

Safety Data

• Hazardous Substances Data: 93489-14-6(Hazardous Substances Data)

Usage

General Description

3-Methoxy-4-Ethoxybenzylamine is a chemical compound that consists of a benzene ring with a methoxy and an ethoxy group attached to the fourth carbon, and an amine group attached to the third carbon. 3-METHOXY-4-ETHOXYBENZYLAMINE is commonly used in organic synthesis and as a building block to create more complex chemical structures. It can also be used as a reagent in the production of pharmaceuticals and agrochemicals. Additionally, 3-Methoxy-4-Ethoxybenzylamine has potential applications in the fields of medicinal chemistry and drug discovery due to its unique chemical structure and potential biological activity.

Upstream product

• 120-25-2 4-ethoxy-3-methoxybenzaldehyde 
• 247569-93-3 4-ethoxy-3-methoxy-benzoic acid amide 
• 3535-24-8 4-ethoxy-3-methoxybenzoic acid methyl ester 
• 121-34-6 3-methoxy-4-hydroxybenzoic acid 
• 3535-30-6 4-ethoxy-3-methoxybenzoic acid 
• 3943-74-6 4-hydroxy-3-methoxybenzoic acid methyl ester 
• 944256-01-3 C₁₅H₂₃NO₄ 
• 81259-56-5 4-ethoxy-3-methoxybenzonitrile 

Downstream Products

• 1149587-52-9 ethyl 2-[5-bromo-4-(4-ethoxy-3-methoxybenzylamino)-6-oxopyridazin-1(6H)-yl]acetate 

Relevant articles and documents

Ultra-small cobalt nanoparticles from molecularly-defined Co-salen complexes for catalytic synthesis of amines

We report the synthesis of in situ generated cobalt nanoparticles from molecularly defined complexes as efficient and selective catalysts for reductive amination reactions. In the presence of ammonia and hydrogen, cobalt-salen complexes such as cobalt(ii)-N,N′-bis(salicylidene)-1,2-phenylenediamine produce ultra-small (2-4 nm) cobalt-nanoparticles embedded in a carbon-nitrogen framework. The resulting materials constitute stable, reusable and magnetically separable catalysts, which enable the synthesis of linear and branched benzylic, heterocyclic and aliphatic primary amines from carbonyl compounds and ammonia. The isolated nanoparticles also represent excellent catalysts for the synthesis of primary, secondary as well as tertiary amines including biologically relevant N-methyl amines.

Anthranilic acid derivatives as inhibitors of the cGMP-phosphodiesterase

Compounds of formula (I) STR1where R 1 is hydrogen; R 2 is nitro, cyano or halo(lower)alkyl; R 3 is phenyl substituted with one or more substituents selected from halogen, cyano and lower alkoxy; A is a lower alkylene group; R 4 is a group CR 6 R 7 R 8 wherein R 6 and R 7 form, together with the carbon atom to which they are attached a cycloalkyl group optionally substituted with hydroxy, lower alkoxy or a lower alkanoylamino; and R 8 is hydrogen; its prodrug and a salt thereof.