90430-14-1

Basic information

• Product Name: 4-HYDROXYBENZYLAMINE HYDROBROMIDE
• Synonyms: 4-Hydroxybenzylammonium bromide;4-(Aminomethyl)phenol hydrobromide 98%;4-Hydroxybenzylamine hydrobromide, (4-Hydroxyphenyl)methylamine hydrobromide;4-(Aminomethyl)phenolhydrobromide98%;4-AMINOMETHYL-PHENOL HYDROBROMIDE;4-HYDROXY-BENZYLAMINE HBR;4-HYDROXYBENZYLAMINE HYDROBROMIDE;(4-HYDROXYPHENYL)METHANAMINIUM BROMIDE
• CAS NO: 90430-14-1
• Molecular Formula: BrH*C₇H₉NO
• Molecular Weight: 204.06
• Mol File: 90430-14-1.mol
• Article Data: 6

Chemical Properties

• Melting Point: 200-203°C
• Boiling Point: 262.4°Cat760mmHg
• Flash Point: 112.5°C
• Appearance: /
• Density: g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-HYDROXYBENZYLAMINE HYDROBROMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-HYDROXYBENZYLAMINE HYDROBROMIDE(90430-14-1)
• EPA Substance Registry System: 4-HYDROXYBENZYLAMINE HYDROBROMIDE(90430-14-1)

Safety Data

• Hazard Codes: C
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 90430-14-1(Hazardous Substances Data)

Usage

General Description

4-Hydroxybenzylamine hydrobromide is a chemical compound that is commonly used in organic synthesis and pharmaceutical research. It is a derivative of benzylamine, a primary amine. The hydrobromide salt form of this compound is often used in the synthesis of various pharmaceuticals and as a building block for organic reactions. It may also have applications in the treatment of certain medical conditions, although further research is needed to fully understand its potential pharmacological properties. Overall, 4-hydroxybenzylamine hydrobromide is a valuable compound with important applications in the fields of chemistry and medicine.

Upstream product

• 2393-23-9 4-methoxy-benzylamine 

Downstream Products

• 852815-05-5 3-[4-(1,1-dimethylethyl)phenyl]-N-[(4-hydroxyphenyl)methyl]-1-methyl-1H-pyrazole-5-carboxamide 
• 1380401-33-1 tert-butyl N-{[4-(prop-2-yn-1-yloxy)phenyl]methyl}carbamate 
• 890042-55-4 2-[2-chloro-4-(6-oxo-1,4,5,6-tetrahydro-pyridazin-3-yl)-phenoxy]-N-(4-hydroxybenzyl)-acetamide 
• 909901-13-9 biphenyl-2-ylcarbamic acid 1-(3-{3-[3-(4-hydroxybenzylamino)propyl]-2-oxoimidazolidin-1-yl}propyl)piperidin-4-yl ester 
• 866915-88-0 (4-{4'-[4-(tert-butoxycarbonylamino-methyl)-phenoxy]-1,1'-dioxy-[2,2']bipyridinyl-4-yloxy}-benzyl)-carbamic acid tert-butyl ester 
• 149505-94-2 tert-butyl (4-hydroxybenzyl)carbamate 

Relevant articles and documents

Post-synthetic modifications of cadmium-based knots and links

Three topologically non-trivial cadmium(ii)-based complexes - Cd-[2]C, Cd-TK and Cd-SL - were simultaneously self-assembled in a dynamic library, individually isolated and fully characterized using solid-state, gas-phase and solution-phase techniques. Post-synthetic modifications, including reduction and transmetalation, were subsequently achieved. Imine bond reduction followed by demetallation led to the isolation of the corresponding organic molecules [2]C, TK and SL. Transmetalation of Cd-TK and Cd-SL with the zinc(ii) cation resulted in isolation of the corresponding zinc(ii)-containing complexes Zn-TK and Zn-SL.

Simultaneous self-assembly of a [2]catenane, a trefoil knot, and a solomon link from a simple pair of ligands

A topological triptych: Three molecular links, a [2]catenane, a trefoil knot, and a Solomon link, were obtained in one pot through the self-assembly of two simple ligands in the presence of ZnII (see picture). The approach relied on dynamic covalent chemistry and metal templation.

Triazolo[4,5-D]pyrimidinyl derivatives and their use as medicaments

The invention relates to triazolo[4,5-d]pyrimidin-3-yl derivatives which are useful in the treatment of platelet aggregation disorders.