155697-42-0

Usage

Uses

Since the provided materials do not specify the exact applications of 2-Propen-1-ol, 3-[3-(phenylmethoxy)phenyl]-, (2E)-, I will list some potential uses based on its chemical properties and the general applications of stilbenes:
Used in Pharmaceutical Industry:
2-Propen-1-ol, 3-[3-(phenylmethoxy)phenyl]-, (2E)can be used as a pharmaceutical intermediate for the synthesis of various drugs and pharmaceutical compounds. Its unique structure and functional groups may contribute to the development of new therapeutic agents.
Used in Agrochemical Industry:
2-Propen-1-ol, 3-[3-(phenylmethoxy)phenyl]-, (2E)may also find applications in the agrochemical industry as a precursor for the synthesis of pesticides, herbicides, or other agrochemicals. Its specific properties and reactivity could be utilized to create new and effective products.
Used in Flavor and Fragrance Industry:
Due to its aromatic nature, 2-Propen-1-ol, 3-[3-(phenylmethoxy)phenyl]-, (2E)could be used as a component in the flavor and fragrance industry to create unique scents or flavors for various products.
Used in Dye and Pigment Industry:
2-Propen-1-ol, 3-[3-(phenylmethoxy)phenyl]-, (2E)-'s chemical structure may also allow it to be used in the dye and pigment industry for the development of new colorants or dyes for various applications, such as textiles, plastics, or printing inks.

Upstream product

• 208836-69-5 3-(3'-benzyloxyphenyl)-(E)-propenoic acid ethyl ester 
• 1700-37-4 3-Benzyloxybenzaldehyde 
• 122024-75-3 3-<3-(phenylmethoxy)phenyl>-2-propenoic acid 
• 1026884-98-9 benzyl (E)-3'-benzyloxycinnamate 
• 14755-02-3 3-hydroxy-trans-cinnamic acid 
• 96251-92-2 (E)-3-(3-hydroxyphenyl)acrylic acid ethyl ester 
• 100-39-0 benzyl bromide 

Downstream Products

• 155697-43-1 3-(3-Benzyloxy-phenyl)-pent-4-enoic acid ethyl ester 
• 850307-91-4 (E)-3-[2,4-bis(benzyloxy)-6-hydroxyphenyl]-1-(3-benzyloxyphenyl)propene 
• 1384457-48-0 (2E)-3-(3-benzyloxyphenyl)prop-2-en-1-yl propionate 
• 175591-09-0 tapentadol hydrochloride 
• 1384457-51-5 (αR,βR)-β-ethyl-3-hydroxy-N,N,α-trimethylbenzenepropanamide 
• 1384457-44-6 (2R,3R)-3-(3-benzyloxyphenyl)-2-methylpent-4-enoic acid 
• 1384457-45-7 (2R,3R)-3-(3-benzyloxyphenyl)-2-methylpent-4-enoic acid (R)-1-phenylethylamine salt 
• 1384457-52-6 (1R,2R)-3-(3-hydroxyphenyl)-2-methyl-pentanoic acid 
• 1384457-50-4 (2R,3R)-3-(3-hydroxyphenyl)-2-methylpentanoic acid chloride 
• 175591-23-8 tapentadol 
• 1443156-34-0 (2R,3R)-3-(3-(benzyloxy)phenyl)-2-methylpent-4-enal 
• 1367878-83-8 (2R,3R)-3-(3-(benzyloxy)phenyl)-N,N,2-trimethylpent-4-en-1-amine 
• 1443156-35-1 (2R,3R)-3-(3-(benzyloxy)phenyl)-N,N,2-trimethylpent-4-en-1-amine hydrochloride 
• 1443156-32-8 (E)-1-(3-(allyloxy)prop-1-enyl)-3-(benzyloxy)benzene 

Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESIS OF TAPENTADOL AND ITS SALTS

A process for the synthesis of a salt of tapentadol.

O-SUBSTITUTED (2R,3R)-3-(3-HYDROXYPHENYL)-2-METHYL-4-PENTENOIC ACIDS AND A METHOD OF OBTAINING THE SAME

The compounds of general formula II are new and represent important intermediates in the synthesis of tapentadol. In the synthesis of tapentadol of formula I and its pharmaceutically acceptable salts, O-protected (2R,3R)-acids of general formula II, in step A, are reacted in an inert organic solvent with an activating agent, optionally in presence of a catalyst or a base; in step B, the obtained compounds of general formula V, wherein R has the above mentioned meaning and X stands for chlorine or alkoxycarbonyloxyl group O-CO-OR1 or pivaloyloxyl O-CO-t-Bu group, wherein R1 is methyl or ethyl, are reacted with dimethylamine or its salts optionally in presence of a base; in step C, the obtained N, N-dimethylamides of general formula VI, wherein R has the above mentioned meaning, are reduced by means of hydride agents in a suitable solvent; in step D, the produced alkeneamines of general formula VII, wherein R has the above mentioned meaning, are hydrogenated on a metal catalysts in a suitable solvent; and, finally, in step E, the produced alkaneamines of general formula VIII, wherein R has the above mentioned meaning, are O-dealkylated by means of dealkylating agents, and, if required, the obtained tapentadol is converted by the action of a pharmaceutically acceptable acid to respective salts, e.g. hydrochloride.

Fluorinated amino acids Part 2: Synthesis of diastereomeric N-acyloxazolidinone precursors

Evans' chiral auxiliary is used to resolve 3-difluoromethyl-3-(3-benzyloxyphenyl)propionic acid (8), which provides key building blocks for the synthesis of chiral β-substituted m-tyrosine derivatives.