289657-26-7

Basic information

• Product Name: (R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol
• Synonyms: (R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol
• CAS NO: 289657-26-7
• Molecular Weight: 496.649
• Mol File: 289657-26-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol(289657-26-7)
• EPA Substance Registry System: (R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol(289657-26-7)

Safety Data

• Hazardous Substances Data: 289657-26-7(Hazardous Substances Data)

Usage

Description

(R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol is a complex organic compound characterized by its multiple functional groups, including an amino group, a benzene ring, a methoxyphenyl group, a phenylmethoxy group, an alcohol group, and a chiral center denoted by the (R,R) configuration. (R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol's structural complexity and diverse functional groups suggest potential applications in various fields, although further research is necessary to determine its specific properties and uses.

Uses

Used in Pharmaceutical Industry:
(R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol is used as a potential pharmaceutical compound for its diverse functional groups that may interact with biological targets, potentially leading to the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol can be utilized as a starting material or a building block for the synthesis of more complex molecules with specific applications in various industries.
Used in Material Science:
(R,R)-3-amino-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenyl methyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol's unique structure and functional groups may also find applications in material science, where it could be used to develop new materials with tailored properties for use in various technologies.

Upstream product

• 1049695-95-5 benzyl-[2-(4-methoxy-phenyl)-1-methyl-ethyl]-amine; hydrochloride 
• 1198769-18-4 (R)-4-benzyloxy-3-nitro-α-(N-benzyl-N-(1-methyl-2-p-methoxyphenylethyl)amino)acetophenone 
• 245759-64-2 (R)-N-benzyl-N-(1-methyl-2-p-methoxyphenylethyl)amine L-mandelate 
• 1096141-37-5 C₁₇H₁₉NO 
• 43229-65-8 [2-(4-methoxyphenyl)-1-methylethyl](phenylmethyl)amine 
• 122-84-9 4-methoxybenzyl methyl ketone 
• 100-46-9 benzylamine 
• 188690-82-6 (R)-2-bromo-1-(4-benzyloxy-3-nitrophenyl)ethanol 
• 188730-94-1 (R)-1-(4-benzyloxy-3-nitrophenyl)oxirane 
• 67346-60-5 (R)-(-)-1-(4'-methoxyphenyl)-2-benzylaminopropane 
• 43229-01-2 4-benzyloxy-3-nitrophenacyl bromide 
• 245759-65-3 (R,R)-3-nitro-α-[[[2-(4-methoxyphenyl)-1-methylethyl](phenylmethyl)amino]methyl]-4-(phenylmethoxy)-benzenemethanol 

Downstream Products

• 73573-87-2 (R,R)-formoterol 
• 188690-83-7 N-[5-[(1R)-Hydroxy-2-[[(1R)-methyl-2-(4-methoxyphenyl)ethyl](phenylmethyl)amino]ethyl]-2-(phenylmethoxy)phenyl]-formamide 

Relevant articles and documents

Preparation method of arformoterol tartrate important intermediate

The invention relates to a preparation method of an arformoterol tartrate important intermediate and belongs to the field of pharmaceutical chemistry. According to the method, I is subjected to reduction by the use of iron powder and acetic acid to prepar

PROCESS FOR THE SYNTHESIS OF ARFORMOTEROL

The present invention provides a process for preparing a compound of formula (Vl) or a salt thereof, the process comprising: (i) reacting 4-methoxyphenyl acetone with an amine of formula (VIII) under conditions of reductive amination to produce a compound of formula (II) or a salt thereof, wherein there is no isolation of an imine intermediate formed during the reductive amination; (ii) condensing the compound (II) or the acid addition salt thereof with an α-haloketone of formula (III) to produce the compound of formula (IV); (iii) reducing the compound (IV) to a compound of formula (V); and (iv) reducing the compound (V) to the compound of formula (Vl), wherein the reduction is carried out in the presence of either (1 ) a hydrogen donating compound in the presence of a hydrogen transfer catalyst; or (2) ammonium formate using a hydrogenation catalyst, wherein: R1 and R2 are independently optionally substituted arylalkyl, and Hal is selected from chloro or bromo.