31197-69-0

Basic information

• Product Name: ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE
• Synonyms: ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE;Ethyl α-CyclohexylMandelate;α-Cyclohexyl-α-hydroxy-benzeneacetic Acid Ethyl Ester
• CAS NO: 31197-69-0
• Molecular Formula: C₁₆H₂₂O₃
• Molecular Weight: 262.34
• Product Categories: Aromatics Compounds;Aromatics
• Mol File: 31197-69-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), Ethyl Acetate (Slightly)
• CAS DataBase Reference: ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE(31197-69-0)
• EPA Substance Registry System: ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE(31197-69-0)

Safety Data

• Hazardous Substances Data: 31197-69-0(Hazardous Substances Data)

Usage

Description

ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE, with the CAS number 31197-69-0, is a light yellow oil compound that is primarily utilized in organic synthesis. It is known for its unique chemical properties that make it a valuable component in the creation of various organic compounds.

Uses

Used in Organic Synthesis:
ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and properties allow it to be a versatile building block in the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE is used as a starting material for the development of new drugs. Its chemical properties make it suitable for the synthesis of complex molecules with potential therapeutic effects.
Used in Chemical Research:
ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE is also used in chemical research as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. This helps researchers gain a deeper understanding of chemical processes and improve the efficiency of organic synthesis.
Used in Flavor and Fragrance Industry:
Due to its unique chemical structure, ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE can be used as a component in the creation of new fragrances and flavors. Its light yellow oil form and distinct properties make it a valuable addition to the flavor and fragrance industry.

Upstream product

• 1603-79-8 phenylglyoxylic acid ethyl ester 
• 931-50-0 cyclohexylmagnesium bromide 
• 626-62-0 Cyclohexyl iodide 
• 774-40-3 hydroxy-phenyl-acetic acid ethyl ester 

Downstream Products

• 94439-61-9 Cyclohexyl-phenyl-glykolsaeure-<2-dimethylamino-propylester> 
• 712-50-5 Cyclohexyl phenyl ketone 
• 7638-50-8 Cyclohexyl-phenyl-glykolsaeure-<2-(N,N-dimethyl-hydrazonio)-aethylester> 
• 25520-98-3 cyclohexyl-hydroxy-phenyl-acetic acid-(2-dimethylamino-ethyl ester) 
• 14657-85-3 Cyclohexyl-phenyl-glykolsaeure-<2-brom-aethylester> 
• 3570-96-5 demethyloxyphenonium 
• 50-10-2 oxyphenonium bromide 
• 712356-35-9 (1α, 5α, 6α)-6-N-(3-azabicyclo [3.1.0] cyclohexyl)-2-hydroxy-2-cyclohexyl-2-phenyl acetamide 
• 712355-73-2 (1α, 5α, 6α)-6-N-(3-azabicyclo [3.1. 0] hexyl-3-benzyl)-2-cyclohexyl-2-hydroxy-2-phenyl acetamide 
• 29125-54-0 Cyclohexyl-hydroxy-phenyl-acetic acid 1-aza-bicyclo[2.2.2]oct-3-yl ester 
• 4335-77-7 cyclohexylmandelic acid 

Relevant articles and documents

OLIGOMER-ANTICHOLINERGIC AGENT CONJUGATES

The invention provides anticholinergic agents that are chemically modified by covalent attachment of a water-soluble oligomer. A conjugate of the invention, when administered by any of a number of administration routes, exhibits characteristics that are different as compared to the characteristics of the anticholinergic agent not attached to the water-soluble oligomer.

Ethyl Mandelate as a Convenient New Benzoyl Anion Equivalent

Ethyl mandelate acts as a convenient benzoyl anion equivalent for the formation of alkyl aryl ketones by deprotonation-alkylation followed by flash vacuum pyrolysis.