934842-69-0

Basic information

• Product Name: 4-Hydroxy-alpha1-[[[6-(4-phenylbutoxy)hexyl](phenylmethyl)amino]methyl]-1,3-benzenedimethanol
• Synonyms: 4-(2-(Benzyl(6-(4-phenylbutoxy)hexyl)amino)-1-hydroxyethyl)-2-(hydroxymethyl)phenol;4-Hydroxy-alpha1-[[[6-(4-phenylbutoxy)hexyl](phenylmethyl)amino]methyl]-1,3-benzenedimethanol; 1,3-BENZENEDIMETHANOL, 4-HYDROXY-A1-[[[6-(4-PHENYLBUTOXY)HEXYL](PHENYLMETHYL)AMINO]METHYL]-
• CAS NO: 934842-69-0
• Molecular Formula: C₃₂H₄₃NO₄
• Molecular Weight: 505.695
• Mol File: 934842-69-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 662.1±55.0 °C(Predicted)
• Appearance: /
• Density: 1.125
• PKA: 9.96±0.31(Predicted)
• CAS DataBase Reference: 4-Hydroxy-alpha1-[[[6-(4-phenylbutoxy)hexyl](phenylmethyl)amino]methyl]-1,3-benzenedimethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Hydroxy-alpha1-[[[6-(4-phenylbutoxy)hexyl](phenylmethyl)amino]methyl]-1,3-benzenedimethanol(934842-69-0)
• EPA Substance Registry System: 4-Hydroxy-alpha1-[[[6-(4-phenylbutoxy)hexyl](phenylmethyl)amino]methyl]-1,3-benzenedimethanol(934842-69-0)

Safety Data

• Hazardous Substances Data: 934842-69-0(Hazardous Substances Data)

Usage

Description

4-Hydroxy-alpha1-[[[6-(4-phenylbutoxy)hexyl](phenylmethyl)amino]methyl]-1,3-benzenedimethanol is a complex organic chemical compound characterized by a long and intricate molecular structure. It features hydroxy, benzene, phenyl, and amine functional groups, along with multiple carbon chains of varying lengths. As a type of benzenedimethanol, this compound is expected to have potential applications in the pharmaceutical or biological fields due to its sophisticated structure and functional groups. However, further research and analysis are required to fully comprehend its possible uses and properties.

Uses

Used in Pharmaceutical Industry:
4-Hydroxy-alpha1-[[[6-(4-phenylbutoxy)hexyl](phenylmethyl)amino]methyl]-1,3-benzenedimethanol is used as a potential pharmaceutical agent for [specific application reason, if available] due to its complex structure and the presence of various functional groups that may interact with biological targets.
Used in Research and Development:
In the field of chemical research and development, 4-Hydroxy-alpha1-[[[6-(4-phenylbutoxy)hexyl](phenylmethyl)amino]methyl]-1,3-benzenedimethanol serves as a subject for studying the synthesis, properties, and potential applications of complex organic compounds with multiple functional groups and carbon chains.

Upstream product

• 163923-19-1 2-hydroxy-5-<<<6,6-(4-phenylbutoxy)hexylbenzyl>amino>acetyl>benzaldehyde 
• 629-03-8 1 ,6-dibromohexane 
• 3360-41-6 4-phenyl-butan-1-ol 
• 90-02-8 salicylaldehyde 
• 115787-50-3 5-(2-bromoacetyl)-2-hydroxybenzaldehyde 
• 94749-73-2 6-bromohexyl 4-phenylbutyl ether 
• 97664-55-6 N-[6-(4-phenylbutoxy)hexyl]benzenemethanamine 

Downstream Products

• 89365-50-4 salmeterol 
• 135271-49-7 salmeterol xinafoate 

Relevant articles and documents

Preparation method of salmeterol base

The invention discloses a preparation method of salmeterol. The method includes the following steps: carrying out a condensation reaction on a compound 2 and a compound 3 under an alkaline condition to obtain an intermediate 4; carrying out acidic hydrolysis to obtain an intermediate 5, and reducing the intermediate 5 to obtain an intermediate 6; and removing a benzyl group from the intermediate 6 by using palladium on carbon (Pd/C) to obtain a salmeterol base. The preparation method has the advantages of mild reaction conditions, simple post-treatment, low cost, high yield high product purity, and easiness in realization of industrialization.

PROCESS FOR THE PREPARATION OF SALMETEROL XINAFOATE

The present invention relates to an improved process for the preparation of Salmeterol Xinafoate of Formula (I).

A new synthetic approach to salmeterol

In the present work a short and convenient route for the synthesis of salmeterol from salicylaldehyde has been developed.