14203-46-4

Basic information

• Product Name: 1,3-Cyclohexanedione, 4-methyl-
• CAS NO: 14203-46-4
• Molecular Formula: C7H10O2
• Molecular Weight: 126.155
• Mol File: 14203-46-4.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: 1,3-Cyclohexanedione, 4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Cyclohexanedione, 4-methyl-(14203-46-4)
• EPA Substance Registry System: 1,3-Cyclohexanedione, 4-methyl-(14203-46-4)

Safety Data

• Hazardous Substances Data: 14203-46-4(Hazardous Substances Data)

Usage

Type of compound

Cyclic diketone

Primary use

Intermediate in the synthesis of other organic compounds

Odor

Mild, slightly sweet

Physical state at room temperature

Colorless to yellowish liquid

Environmental impact

Potential environmental contaminant

Bioaccumulation potential

Low

Acute toxicity

Low

Carcinogenicity

Not classified as a carcinogen

Applications

Versatile chemical with a wide range of applications in synthesis and research

Upstream product

• 70432-50-7 ethyl 5-oxoheptanoate 
• 141-52-6 sodium ethanolate 
• 74650-83-2 methyl α-methyl-γ-carboethoxy-γ-acetylbutyrate 
• 496-73-1 4-methyl resorcinol 
• 36045-56-4 methyl-4 oxo-5 hexanoate de methyle 
• 4054-96-0 5,6-Dimethyl-3,4-dihydro-2-pyrone 
• 60067-95-0 6-methyl-3-(2-methylpropoxy)cyclohex-2-en-1-one 
• 504-02-9 1,3-cylohexanedione 
• 74-88-4 methyl iodide 
• 84488-23-3 8-methyl-1,4-dioxaspiro<4,5>decan-7-one 
• 124015-80-1 3-(N',N'-Dimethyl-hydrazino)-4-methyl-cyclohex-2-enone 
• 84488-25-5 10-Methyl-1,4-dioxa-spiro[4.5]decan-7-one 
• 67-64-1 acetone 
• 97-88-1 2-methyl-butyl acrylate 

Downstream Products

• 87994-96-5 3-ethoxy-4-methylcyclohex-2-enone 
• 119138-61-3 4-methyl cyclohexane-1,3-diol 
• 122571-21-5 2-Diazo-4-methylcyclohexane-1,3-dione 
• 81465-54-5 3-Iodo-4-methyl-cyclohex-3-enone 
• 81465-40-9 3-iodo-6-methyl-2-cyclohexen-1-one 
• 81465-48-7 3-Iodo-4-methyl-cyclohex-2-enone 
• 69841-15-2 meso-4,6-dimethylcyclohexane-1,3-dione 
• 113924-35-9 5-methyl-4-oxo-1-phenyl-2,3,4,5,6,7-hexhydrobenzofuran 
• 113924-36-0 7-methyk-4-oxo-1-phenyl-2,3,4,5,6,7-hexahydrobenzofuran 
• 67025-06-3 3-methoxy-6-methyl-2-cyclohexenone 
• 53483-54-8 6-Methyl-3-phenylamino-cyclohex-2-enone 
• 1355249-13-6 C₁₆H₁₇BrN₂O₂ 
• 1355249-12-5 C₁₆H₁₇BrN₂O₂ 

Relevant articles and documents

SOLID FORMS OF 2-(TERT-BUTYLAMINO)-4-((1R,3R,4R)-3-HYDROXY-4-METHYLCYCLOHEXYLAMINO)-PYRIMIDINE-5-CARBOXAMIDE, COMPOSITIONS THEREOF AND METHODS OF THEIR USE

Provided herein are formulations, processes, solid forms and methods of use relating to 2- (tert-butylamino)-4-((lR,3R,4R)-3-hydroxy-4-methylcyclohexylamino)-pyrimidine-5- carboxamide.

SUBSTITUTED CYCLOHEXANE-1, 3-DIONE COMPOUNDS, PROCESS FOR PREPARATION THEREOF AND ITS APPLICATIONS

A regio-selective and consecutive Michael-Claisen process has been developed for substituted cyclohexane-1,3-dione synthesis started from unsubstituted or substituted acetone and α,β-unsaturated esters. Substituted cyclohexane-1,3-diones are the basic uni

Tandem reactions leading to benzo[c]chromen-6-ones and 3-substituted isocoumarins

A simple and convenient protocol for the synthesis of benzo[c]chromen-6- ones and 3-substituted isocoumarins through a CuI-catalyzed tandem reaction of 2-bromobenzoates withcyclohexane-1,3-diones or acyclic 1,3-diones is developed. This strategy can also be extended to the one-pot synthesis of isoquinolin-1(2H)-one and 3,4-dihydrophenanthridine-1,6(2H,5H)-dione. A simple and convenient protocol for the synthesis of benzo[c]chromen-6-ones and 3-substituted isocoumarins through a CuI-catalyzed tandem reaction of 2-bromobenzoates with cyclohexane-1,3-dione or acyclic 1,3-dione has been developed. This strategy can also be extended to the one-pot synthesis of isoquionlin-1(2H)-one and 3,4-dihydrophenanthridine-1,6-(2H,5H)-dione. Copyright