215316-59-9

Basic information

• Product Name: (R)-3-Hydroxy-3-(2-Phenylethyl)Hexanoic Acid
• Synonyms: (R)-3-Hydroxy-3-(2-Phenylethyl)Hexanoic Acid
• CAS NO: 215316-59-9
• Molecular Formula: C₁₄H₂₀O₃
• Molecular Weight: 236.3068
• Mol File: 215316-59-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-3-Hydroxy-3-(2-Phenylethyl)Hexanoic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-Hydroxy-3-(2-Phenylethyl)Hexanoic Acid(215316-59-9)
• EPA Substance Registry System: (R)-3-Hydroxy-3-(2-Phenylethyl)Hexanoic Acid(215316-59-9)

Safety Data

• Hazardous Substances Data: 215316-59-9(Hazardous Substances Data)

Usage

Uses

Used in Perfumery and Cosmetics:
(R)-3-Hydroxy-3-(2-Phenylethyl)Hexanoic Acid is used as a fragrance ingredient for its pleasant aroma, contributing to the overall scent profile of perfumes and cosmetics. Its natural origin and appealing scent make it a popular choice in the fragrance industry.
Used in Food and Beverage Industry:
(R)-3-Hydroxy-3-(2-Phenylethyl)Hexanoic Acid is used as a flavoring agent for its characteristic fruity taste, enhancing the flavor of various food and beverage products. Its natural presence in fruits and its ability to impart a desirable taste make it a valuable addition to the flavor industry.
Used in Health and Wellness Applications:
(R)-3-Hydroxy-3-(2-Phenylethyl)Hexanoic Acid is being researched for its potential health benefits, such as aiding in weight loss and improving metabolic function. While more research is needed to fully understand its effects on the human body, raspberry ketone has shown promise as a natural supplement for health and wellness.

Upstream product

• 215316-49-7 3-hydroxy-3-(2'-phenylethyl)hexanoic acid 

Downstream Products

• 215317-08-1 (R)-(4-phenylphenoxy)methyl-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanoate 
• 174484-41-4 tipranavir 
• 174485-90-6 (R)-3-[(R)-1-(3-Amino-phenyl)-propyl]-4-hydroxy-6-phenethyl-6-propyl-5,6-dihydro-pyran-2-one 
• 215317-11-6 (R)-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanol 
• 215317-14-9 (R)-3-(2-phenylethyl)-3-[(4-phenylphenoxy)methoxy]hexanal 
• 215317-22-9 (6R)-4-hydroxy-3-[1-(3-nitrophenyl)-1-propyl]-6-phenethyl-6-propyl-5,6-dihydro-2H-pyran-2-one 
• 215317-20-7 (R)-5-Hydroxy-2-[(S)-1-(3-nitro-phenyl)-propyl]-3-oxo-5-phenethyl-octanoic acid methyl ester 
• 215317-17-2 (R)-5-(Biphenyl-4-yloxymethoxy)-3-hydroxy-2-[(S)-1-(3-nitro-phenyl)-propyl]-5-phenethyl-octanoic acid methyl ester 
• 215317-19-4 (R)-5-(Biphenyl-4-yloxymethoxy)-2-[(S)-1-(3-nitro-phenyl)-propyl]-3-oxo-5-phenethyl-octanoic acid methyl ester 
• 577979-85-2 (R)-3-hydroxy-1-(1-imidazolyl)-3-(2-phenylethyl)hexane-1-one 

Relevant articles and documents

Process for the synthesis of an antiviral compound

In a process comprising synthesizing pyranes including [R—(R*,R*)]-N-[3-[1-[5,6-dihydro-4-hydroxy-2-oxo-6-(2-phenylethyl)-6-propyl-2H-pyran-3-yl]propyl]phenyl]-5-(trifluoromethyl)-2-pyridinesulfonamide the present invention comprises the improvements comp

Production method of (R) -3 hydroxy-3- (2-phenylethyl) hexanoic acid and intermediate thereof

The present invention relates to a production method of (R)-3-hydroxy-3-(2-phenylethyl)hexanoic acid which comprises optical resolution of racemic 3-hydroxy-3-(2-phenylethyl)hexanoic acid with an optically active amine of the formula (VIII) 1wherein R2 is 3,4-dimethoxyphenyl or 2-chlorophenyl. According to the present invention, (R)-3-hydroxy-3-(2-phenylethyl)hexanoic acid useful as a starting material of a pharmaceutical agent can be efficiently produced with a high optical purity and a relatively high total yield.