73640-74-1

Basic information

• Product Name: 4'-BENZYLOXY-2'-HYDROXY-3'-METHYLACETOPHENONE
• Synonyms: 1-[4-(BENZYLOXY)-2-HYDROXY-3-METHYLPHENYL]ETHAN-1-ONE;4'-BENZYLOXY-2'-HYDROXY-3'-METHYLACETOPHENONE;LABOTEST-BB LT00453052
• CAS NO: 73640-74-1
• Molecular Formula: C₁₆H₁₆O₃
• Molecular Weight: 256.3
• Mol File: 73640-74-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 88-90 °C(lit.)
• Appearance: /
• CAS DataBase Reference: 4'-BENZYLOXY-2'-HYDROXY-3'-METHYLACETOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-BENZYLOXY-2'-HYDROXY-3'-METHYLACETOPHENONE(73640-74-1)
• EPA Substance Registry System: 4'-BENZYLOXY-2'-HYDROXY-3'-METHYLACETOPHENONE(73640-74-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• WGK Germany: 3
• Hazardous Substances Data: 73640-74-1(Hazardous Substances Data)

Usage

Preparation

Preparation by reaction of benzyl chloride on 2,4-di-hydroxy-3-methylacetophenone with potassium carbonate and potassium iodide in refluxing acetone (81%).

Upstream product

• 10139-84-1 1-(2,4-dihydroxy-3-methylphenyl)ethanone 
• 100-44-7 benzyl chloride 
• 608-25-3 2-methylbenzene-1,3-diol 

Downstream Products

• 130736-29-7 2-(dimethylamino)-8-methyl-7-(phenylmethoxy)-4H-1-benzopyran-4-one 
• 118824-96-7 4'-Benzyloxy-2'-methoxy-3'-methylacetophenone 
• 90515-38-1 7-(benzyloxy)-4-hydroxy-8-methyl-2H-chromen-2-one 
• 869989-22-0 7-(benzyloxy)-4-hydroxy-8-methyl-3-nitro-2H-chromen-2-one 
• 869989-26-4 7-benzyloxy-2,6-dimethylchromeno[3,4-d]oxazol-4-one 
• 869989-24-2 N-(7-benzyloxy-4-hydroxy-8-methyl-2-oxo-(2H)-chromen-3-yl)-acetamide 
• 118824-97-8 4'-Hydroxy-2'-methoxy-3'-methylacetophenone 
• 118824-98-9 4'-Hydroxy-2'-methoxy-3'-methyl-5'-nitroacetophenone 
• 130737-44-9 8-Methyl-7-(phenylmethoxy)-2-mercapto-4H-1-benzopyran-4-one 

Relevant articles and documents

2-AMINOPYRIDINE DERIVATIVE

The invention relates to a compound useful as remedies or preventives for IKK2-related inflammatory diseases or autoimmune diseases, or that is, a 2-aminopyrimidine derivative having a 2-hydroxyphenyl group at the 6-position thereof and having a saturated

Synthesis of Indolin-2-ones (Oxindoles) Related to Mitomycin A

Oxindoles (indolin-2-ones) containing the functionality of the first two rings of the mytomicin A structure have been synthesized.Attempts to employ the oxindole grouping to construct the third ring were unsuccessful because of the resistance of the oxindole group or its derivatives towards nucleophilic attack.An unusual methylation of 3-methyl-5-nitrobenzene-1,2,4-triol to give the (E)-3,6-dihydroxy-2-methyl-1,4-benzoquinone 4-methoxyimine N-oxide is noted.A novel indole formation is described.