92243-37-3

Basic information

• Product Name: (1S,2R_.5S)-2-isopropyl-5-methylcyclohexyl 2-methoxybenzoate
• Synonyms: (1S,2R_.5S)-2-isopropyl-5-methylcyclohexyl 2-methoxybenzoate
• CAS NO: 92243-37-3
• Molecular Weight: 290.403
• Mol File: 92243-37-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (1S,2R_.5S)-2-isopropyl-5-methylcyclohexyl 2-methoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R_.5S)-2-isopropyl-5-methylcyclohexyl 2-methoxybenzoate(92243-37-3)
• EPA Substance Registry System: (1S,2R_.5S)-2-isopropyl-5-methylcyclohexyl 2-methoxybenzoate(92243-37-3)

Safety Data

• Hazardous Substances Data: 92243-37-3(Hazardous Substances Data)

Upstream product

• 15356-60-2 (1S,2R,5S)-(+)-menthol 
• 21615-34-9 2-Methoxybenzoyl chloride 
• 119-36-8 methyl salicylate 
• 69-72-7 salicylic acid 
• 2216-51-5 (-)-menthol 
• 579-75-9 2-Methoxybenzoic acid 
• 67392-57-8 (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester of diphenylphosphinous acid 

Downstream Products

• 92243-38-4 2-Methoxy-1-methyl-cyclohexa-2,5-dienecarboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester 

Relevant articles and documents

Synthesis, antimicrobial evaluation, and QSAR analysis of 2-isopropyl-5-methylcyclohexanol derivatives

A series of 2-isopropyl-5-methylcyclohexanol derivatives were synthesized and evaluated for their antibacterial activity against Gram-positive Staphylococcus aureus and Bacillus subtilis and Gram-negative Escherichia coli and in vitro antifungal activity against Candida albicans and Aspergillus niger. The results of antimicrobial activity demonstrated that the compounds 10, 20, and 21 were the most active ones among the synthesized compounds. The QSAR studies revealed the importance of dipole moment (μ), total energy (Te), and topological parameters (κ1 and κ3) in describing the antimicrobial activity of 2-isopropyl-5-methylcyclohexanol derivatives. Springer Science+Business Media, LLC 2011.

Efficient method for the preparation of carboxylic acid alkyl esters or alkyl phenyl ethers by a new-type of oxidation-reduction condensation using 2,6-dimethyl-1,4-benzoquinone and alkoxydiphenylphosphines

A new-type of oxidation-reduction condensation proceeded smoothly to afford carboxylic acid alkyl esters or alkyl phenyl ethers in good to high yields by combined use of alkoxydiphenylphosphines (1) having primary, bulky secondary or tertiary alkoxy groups, a mild quinone-type oxidant such as 2,6-dimethyl-1,4-benzoquinone (DMBQ) and carboxylic acids or phenols. Generally, alkoxydiphenylphosphines were prepared easily from chlorodiphenylphosphine (2) and alcohols in the presence of pyridine, and were isolated by distillation. On the other hand, the phosphines 1 were also prepared in situ from N,N-dimethylaminodiphenylphosphine (3a) and primary or secondary alcohols while primary, bulky secondary or tertiary alkoxydiphenylphosphines were alternatively formed in situ by adding 2 to the "BuLi-treated alcohols in order to perform the above reactions by a one-pot procedure from alcohols and nucleophiles. The reaction of thus formed 1, DMBQ and carboxylic acids or phenols afforded the corresponding alkylated products, including hindered secondary and tertiary alkylated ones, in good to high yields at room temperature. In the case of using chiral secondary alcohols, the corresponding carboxylic acid alkyl esters were obtained as well in high yields with perfect inversion of stereochemistry by SN2 replacement.

Preparation of chiral amine carbonyl chromium(0) complexes with [(norbornadiene)Cr(CO)4] as the complexation reagent

A number of chiral amines were prepared and used as ligands in carbonylchromium(0) complexes. Included are monoamines chelating diamines and methionine methyl ester. For their complexation (norbornadiene)tetracarbonylchromium(0) was found to allow complex