64353-30-6

Basic information

• Product Name: 4-(2-Aminoethyl)phenylmethanol
• Synonyms: [4-(2-AMINO-ETHYL)-PHENYL]-METHANOL
• CAS NO: 64353-30-6
• Molecular Formula: C₉H₁₃NO
• Molecular Weight: 151.21
• Mol File: 64353-30-6.mol
• Article Data: 6

Chemical Properties

• Melting Point: <20 °C
• Boiling Point: 291.9 °C at 760 mmHg
• Flash Point: 130.4 °C
• Appearance: /
• Density: 1.082 g/cm³
• Refractive Index: 1.569
• Storage Temp.: 2-8°C
• PKA: 14.44±0.10(Predicted)
• CAS DataBase Reference: 4-(2-Aminoethyl)phenylmethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-Aminoethyl)phenylmethanol(64353-30-6)
• EPA Substance Registry System: 4-(2-Aminoethyl)phenylmethanol(64353-30-6)

Safety Data

• Hazardous Substances Data: 64353-30-6(Hazardous Substances Data)

Usage

General Description

4-(2-Aminoethyl)phenylmethanol is a chemical compound with the molecular formula C9H13NO. It is an aromatic alcohol that contains an aminoethyl group and a phenyl group. 4-(2-Aminoethyl)phenylmethanol is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It has been studied for its potential therapeutic applications, such as its role in the treatment of various diseases and disorders. Additionally, 4-(2-Aminoethyl)phenylmethanol has been investigated for its potential use as a building block in the production of new materials and chemical products. Overall, this compound has a variety of potential applications in the pharmaceutical and chemical industries due to its unique chemical structure and properties.

InChI:InChI=1/C9H13NO/c10-6-5-8-1-3-9(7-11)4-2-8/h1-4,11H,5-7,10H2

Upstream product

• 77265-67-9 4-(2-amino-ethyl)-benzoic acid methyl ester 
• 52010-97-6 4-(hydroxylmethyl)benzaldehyde 
• 623-27-8 terephthalaldehyde, 
• 2417-72-3 Methyl 4-(bromomethyl)benzoate 
• 99-75-2 4-methyl-benzoic acid methyl ester 
• 76469-88-0 methyl 4-(cyanomethyl)benzoate 
• 1199-69-5 4-(2-aminoethyl)benzoic acid 

Downstream Products

• 68559-71-7 [4-(2-Amino-ethyl)-phenyl]-methanol hydrochloride 
• 64353-37-3 4-(2-aminoethyl)-benzaldehyde-hydrochloride 
• 1402088-38-3 N-(4-(hydroxymethyl)phenethyl)benzamide 
• 1402088-43-0 N-(4-(hydroxymethyl)benzyl)-4-(trifluoromethyl)benzamide 
• 1253889-45-0 N⁽¹⁾-(4-butylphenyl)-N⁽²⁾-(4-(hydroxymethyl)phenethyl)phthalamide 
• 137668-71-4 4-(2-{4-[Hydroxy-(1-methyl-cyclohexyloxy)-phosphorylmethyl]-phenyl}-ethylcarbamoyl)-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester 
• 137668-75-8 4-<2-<<(benzyloxy)carbonyl>amino>ethyl>benzyl bromide 
• 137668-73-6 [4-(2-Amino-ethyl)-benzyl]-phosphonic acid mono-(1-methyl-cyclohexyl) ester 
• 914104-08-8 benzyl {2-[4-(hydroxymethyl)phenyl]ethyl}carbamate 

Relevant articles and documents

A traceless photocleavable linker for the automated glycan assembly of carbohydrates with free reducing ends

We report a traceless photocleavable linker for the automated glycan assembly of carbohydrates with free reducing ends. The reductive-labile functionality in the linker tolerates all commonly used reagents and protocols for automated glycan assembly, as demonstrated with the successful preparation of nine plant cell wall-related oligosaccharides, and is cleaved by hydrogenolysis.

Phthalaphos: Chiral supramolecular ligands for enantioselective rhodium-catalyzed hydrogenation reactions

Interligand hydrogen bonding of chiral monodentate phosphite ligands bearing H-bond donor and acceptor groups leads to formation of supramolecular bidentate ligands, rhodium complexes of which (see picture) afford excellent enantiomeric excesses in catalyzed hydrogenation of classical benchmark and industrially relevant substrates. cod=1,5-cyclooctadiene.

Amidine derivatives and cardiotonic compositions

Amidine derivatives of the formula STR1 wherein R1 and R2, which may be the same or different, represent each a hydrogen atom or a lower alkyl group, or R1 and R2 together with an intermediary carbon atom and/or hetero atom may form a ring; X represents STR2 (wherein R8 represents a hydrogen atom, a lower alkyl group, or --CH2 COOR9, where R9 represents a hydrogen atom or a lower alkyl group; Z represents a single bond, --CH2 --, --CH2 CH2 --, or --CH=CH--); R3 represents a hydrogen or chlorine atom, methoxy group, nitro group, or amino group; Y represents --CH2 CH2 --, --CH=CH--, --CH2 O--, or --OCH2 --; R4 represents a hydrogen atom, methoxy group, benzoyl group, nitro group, or amino group; and R5, R6 and R7, which may be the same or different, represent each a hydrogen atom, lower alkyl group, cycloalkyl group, aralkyl group, substituted alkyl group, substituted aralkyl group, or amino group, or R5 and R7 may form a ring, or salts thereof have an excellent cardiotonic activity and can be used as cardiotonics.