64681-98-7

Basic information

• Product Name: dimethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate
• Synonyms: 1,3-cyclohexanedicarboxylic acid, 4-hydroxy-4-methyl-6-oxo-2-phenyl-, dimethyl ester
• CAS NO: 64681-98-7
• Molecular Formula: C₁₇H₂₀O₆
• Molecular Weight: 320.3371
• Mol File: 64681-98-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 461.4°C at 760 mmHg
• Flash Point: 164.4°C
• Density: 1.242g/cm³
• Vapor Pressure: 2.61E-09mmHg at 25°C
• Refractive Index: 1.535
• CAS DataBase Reference: dimethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate(64681-98-7)
• EPA Substance Registry System: dimethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate(64681-98-7)

Safety Data

• Hazardous Substances Data: 64681-98-7(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 105-45-3 acetoacetic acid methyl ester 
• 15768-07-7 methyl 2-benzylidene-3-oxobutanoate 

Downstream Products

• 1176846-02-8 C₂₄H₂₇NO₅ 
• 1013755-52-6 C₂₅H₂₉NO₅ 
• 1013986-40-7 C₂₇H₃₃NO₇ 
• 936079-25-3 dimethyl 4-[2-(1H-indol-3-yl)ethylamino]-6-methyl-2-phenylcyclohexa-3,5-diene-1,3-dicarboxylate 
• 1020373-69-6 5-methoxycarbonyl-6-hydroxy-6-methyl-4-phenyl-4,5,6,7-tetrahydro-3-hydroxy-1H-indazole 
• 94445-22-4 2,4-dimethoxycarbonyl-5-methyl-3-phenylcyclohexan-1-ol 
• 24904-04-9 4,6-dimethoxycarbonyl-3-methyl-5-phenyl-2-cyclohexenone 
• 94445-20-2 2,4-dimethoxycarbonyl-5-methyl-3-phenylcyclohexen-1-one 
• 142592-01-6 1,5-dimethoxycarbonyl-2-methyl-4-morpholino-6-phenyl-1,3-cyclohexadiene 
• 142592-22-1 1,5-dimethoxycarbonyl-2-methyl-6-phenyl-4-piperidino-1,3-cyclohexadiene 

Relevant articles and documents

A mild and convenient one-pot synthesis of 4-aryl-n-oh-hantzsch esters

A general methodology to prepare a series of 4-Aryl-N-OH Hantzsch esters was developed. The key factor is to control the first-step of Michael addition at 0 °C. The method was practical to produce symmetrical and unsymmetric N-OH-Hantzsch esters in moderate yield. This class of compounds might have use in medicinal and material science.

A facile synthesis of 4-aryl-5-alkoxycarbonyl-6-hydroxy-6-methyl-4,5,6,7-tetrahydro-3-hydroxy-2-(pyridin-2-yl)-indazoles and their nmr characterizations

A series of N-pyridinyl tetrahydroindazoles have been synthesized by a convenient and regioseletive method by taking cyclic 2-ketoesters as scaffolds. An optimum reaction condition was achieved by monitoring the reaction in different reaction c

Synthesis and structures of 6-aryl-1,5-dimethoxycarbonyl-2-methyl-4-morpholino-1,3-cyclohexadienes and related compounds

Reaction of benzaldehyde (1a) with methyl acetoacetate (2) in the presence of morpholine (or piperidine) and AcOH in refluxing C6H6 yielded a new condensation product, 1,5-dimethoxycarbonyl-2-methyl-4-morpholino (or piperidino)-6-phe