119927-90-1

Basic information

• Product Name: 2,5-Cyclohexadien-1-one, 3-chloro-4,4-dimethoxy-
• CAS NO: 119927-90-1
• Molecular Formula: C8H9ClO3
• Molecular Weight: 188.611
• Mol File: 119927-90-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2,5-Cyclohexadien-1-one, 3-chloro-4,4-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Cyclohexadien-1-one, 3-chloro-4,4-dimethoxy-(119927-90-1)
• EPA Substance Registry System: 2,5-Cyclohexadien-1-one, 3-chloro-4,4-dimethoxy-(119927-90-1)

Safety Data

• Hazardous Substances Data: 119927-90-1(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 108-43-0 3-monochlorophenol 
• 7073-42-9 N-(3-chloro-4-methoxyphenyl)acetamide 
• 18093-12-4 3-chloro-4-methoxyphenol 

Downstream Products

• 5345-54-0 3-chloro-4-methoxyaniline 
• 18113-14-9 2,5-dichloro-4-methoxyphenol 
• 39542-65-9 2,3-dichloro-4-methoxyphenol 
• 1431660-68-2 C₁₅H₁₂ClNO 
• 1431660-69-3 C₁₅H₁₂ClNO 
• 1431793-58-6 C₁₆H₁₇ClO₅ 
• 132802-68-7 (+/-)-trans-2-(3,4-dimethoxyphenyl)-2,3-dihydro-7-allyl-4-chloro-5-methoxy-3-methylbenzofuran 
• 132802-65-4 2-allyl-5-chloro-4-methoxyphenol 
• 119927-94-5 3-chloro-4,4-dimethoxy-5-phenyl-2-cyclohexenone 

Relevant articles and documents

Synthesis of (+)-Antroquinonol and Analogues by Using Enantioselective Michael Reactions of Benzoquinone Monoketals

(+)-Antroquinonol is an anticancer agent that was first isolated from the rare mushroom Antrodia cinnamomea, which is indigenous to Taiwan. In this study, (+)-antroquinonol is synthesized from benzoquinone monoketals by using an enantioselective Michael r

Synthesis of o-chlorophenols via an unexpected nucleophilic chlorination of quinone monoketals mediated by N,N′-dimethylhydrazine dihydrochloride

An unexpected nucleophilic chlorination of a quinone monoketal while carrying out a pyrazolidine synthesis has led to a general preparation of multisubstituted phenols. The products are obtained in good to high yields under mild conditions. The bridged pyrazolidines that were the original targets are obtained in the presence of a protic solvent. This journal is the Partner Organisations 2014.

Efficient synthesis of oxygenated terphenyls and other oligomers: Sequential arylation reactions through phenol oxidation-rearomatization

One by one: Starting from simple phenols, a diverse series of oxygenated terphenyl compounds can be prepared in a concise and practical manner using sequential arylation reactions involving phenol oxidation/rearomatization and quinone monoacetal intermediates (see scheme). Many of the terphenyl products can be used for preparing well-defined oligomers and, furthermore, contain valuable functional groups that can be transformed for further diversification. Copyright