3886-19-9

Basic information

• Product Name: 1-[2,6-bis(benzyloxy)phenyl]ethanone
• CAS NO: 3886-19-9
• Molecular Formula: C₂₂H₂₀O₃
• Molecular Weight: 332.3924
• Mol File: 3886-19-9.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 492.4°C at 760 mmHg
• Flash Point: 243.9°C
• Density: 1.144g/cm³
• Vapor Pressure: 7.71E-10mmHg at 25°C
• Refractive Index: 1.594
• CAS DataBase Reference: 1-[2,6-bis(benzyloxy)phenyl]ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[2,6-bis(benzyloxy)phenyl]ethanone(3886-19-9)
• EPA Substance Registry System: 1-[2,6-bis(benzyloxy)phenyl]ethanone(3886-19-9)

Safety Data

• Hazardous Substances Data: 3886-19-9(Hazardous Substances Data)

Usage

General Description

1-[2,6-bis(benzyloxy)phenyl]ethanone is a chemical compound with the molecular formula C22H20O3. It is a white solid with a molecular weight of 332.39 g/mol. 1-[2,6-bis(benzyloxy)phenyl]ethanone is commonly used as a building block in organic synthesis and pharmaceutical research. It is a ketone derivative with two benzyloxy groups attached to a phenyl ring, making it a versatile intermediate for the synthesis of various organic compounds. It is also known by its synonyms such as 2,6-bis(benzyloxy)acetophenone and 1-(2,6-bis-(benzyloxy)phenyl)ethanone. 1-[2,6-bis(benzyloxy)phenyl]ethanone is commonly handled and stored in airtight containers away from sources of heat and moisture due to its sensitivity to air and light. Overall, 1-[2,6-bis(benzyloxy)phenyl]ethanone is a valuable chemical in organic synthesis and pharmaceutical research due to its versatile nature and potential for use in various chemical reactions.

Upstream product

• 699-83-2 2,6-dihydroxylacetophenone 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 
• 4047-24-9 1-[2-(benzyloxy)-6-hydroxyphenyl]ethanone 

Downstream Products

• 148356-58-5 2',3,4,6'-tetrakis(benzyloxy)chalcone 
• 148356-57-4 2',4,6'-tris(benzyloxy)chalcone 
• 148356-56-3 2',6'-bis(benzyloxy)chalcone 
• 76799-16-1 2,3',6,-tris(benzyloxy)-4'-methoxychalcone 
• 406212-57-5 tert-butyl 3-{2-amino-6-[2,6-bis(benzyloxy)phenyl]-3-cyano-4-pyridinyl}-1-piperidinecarboxylate 
• 41514-83-4 5-hydroxy-3-phenyl-4H-chromen-4-one 
• 148356-24-5 5-hydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 
• 150436-37-6 5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chroman-4-one 
• 406212-87-1 tert-butyl 2-amino-6-[2,6-bis(benzyloxy)phenyl]-4-[1-(tert-butoxycarbonyl)-3-piperidinyl]nicotinate 
• 1338672-40-4 (E)-1-(2,6-dihydroxyphenyl)-3-(2-hydroxyphenyl)-2-propen-1-one 

Relevant articles and documents

PYRIDINE COMPOUND SUBSTITUTED WITH AZOLE

The present invention provides a compound represented by formula [I] shown below or a pharmaceutically acceptable salt thereof that has an inhibitory effect on 20-HETE producing enzyme. (in formula [I] above, the structure represented by formula [II] below: represents any of the structures represented by formula group [III] below: R1, R2, R3, and R4 independently represent a hydrogen atom, a fluorine atom, methyl, or the like, R5 represents any of the structures represented by formula group [IV]:

Towards the first inhibitors of trihydroxynaphthalene reductase from Curvularia lunata: Synthesis of artificial substrate, homology modelling and initial screening

Trihydroxynaphthalene reductase (3HNR) is an essential enzyme in the biosynthesis of fungal melanin and it represents an emerging target for the development of new fungicides and antimicotics. To promote the discovery of new inhibitors, an improved chemic

Pyridine derivatives

Pyridine compounds of general formula: wherein —R1represents in which R11is hydrogen, C1-6alkyl, halogen, hydroxy, C1-12alkoxy, nitro, amino, C1-6alkylsulfonylamino, C1-6alkoxycarbonyl, C1-6alkylamino, di(C1-6alkyl)amino, C1-6alkanoylamino, phenyl C1-6alkylamino, phenylsulfonylamino, or —O—(CH2)n—R111; R2represents hydrogen or halogen; R3represents hydrogen, —CR31R32R33, or —NR34R35; R4is hydrogen, carbamoyl, CN, carboxyl, etc.; R5is amino, C1-6alkylamino, di C1-6alkylamino, etc. or salt thereof. The compound has an excellent anti-inflammatory activity, and other biological activity.