155419-08-2

Basic information

• Product Name: 1,2-Cyclohexanediol,3-methyl-6-(1-methylethyl)-,[1S-(1alpha,2alpha,3bta,6alpha)]-(9CI)
• Synonyms: 1,2-Cyclohexanediol,3-methyl-6-(1-methylethyl)-,[1S-(1alpha,2alpha,3bta,6alpha)]-(9CI)
• CAS NO: 155419-08-2
• Molecular Formula: C10H20O2
• Molecular Weight: 172.2646
• Product Categories: ISOPROPYL
• Mol File: 155419-08-2.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-Cyclohexanediol,3-methyl-6-(1-methylethyl)-,[1S-(1alpha,2alpha,3bta,6alpha)]-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Cyclohexanediol,3-methyl-6-(1-methylethyl)-,[1S-(1alpha,2alpha,3bta,6alpha)]-(9CI)(155419-08-2)
• EPA Substance Registry System: 1,2-Cyclohexanediol,3-methyl-6-(1-methylethyl)-,[1S-(1alpha,2alpha,3bta,6alpha)]-(9CI)(155419-08-2)

Safety Data

• Hazardous Substances Data: 155419-08-2(Hazardous Substances Data)

Usage

General Description

1,2-Cyclohexanediol,3-methyl-6-(1-methylethyl)-,[1S-(1alpha,2alpha,3beta,6alpha)]-(9CI) is a chemical compound with a unique molecular structure that includes a cyclohexane ring and two hydroxyl groups. It is also known as 3-methyl-6-isopropylcyclohexane-1,2-diol and is classified as a bicyclic alcohol. 1,2-Cyclohexanediol,3-methyl-6-(1-methylethyl)-,[1S-(1alpha,2alpha,3bta,6alpha)]-(9CI) is used in various industrial and research applications, including as a building block for the synthesis of other organic compounds. It may also have potential uses in the pharmaceutical and healthcare industries. The specific stereochemistry of the compound, as indicated by the [1S-(1alpha,2alpha,3beta,6alpha)] designation, is important for its proper identification and application in scientific studies.

Upstream product

• 1753-38-4 2t-Acetoxy-3t-isopropyl-6c-methyl-cyclohexan-1r-ol 
• 93-59-4 Perbenzoic acid 
• 935670-67-0 (1R,2R,6S)-3-methyl-6-(1-methylethenyl)cyclohex-3-ene-1,2-diol 
• 34315-76-9 p-menthane-2,3-dione 
• 2216-51-5 (-)-menthol 
• 5113-93-9 (1R)-trans-p-menth-2-ene 
• 1124-26-1 (+/-)-(3R,6S)-3-isopropyl-6-methyl-1-cyclohexene 
• 1124-26-1 (+/-)-(3R,6R)-3-isopropyl-6-methyl-1-cyclohexene 
• 20747-49-3 (-)-neomenthol 
• 6485-40-1 (R)-Carvone 
• 5206-83-7 (1R,4R)-(+)-carvomenthone 
• 5524-05-0 (2R,5R)-5-isopropenyl-2-methylcyclohexanone 
• 308239-15-8 (1S,2R,3R,6S)-2-hydroxy-3-methyl-6-(methylethyl)cyclohexyl benzoate 
• 308239-17-0 (1R,2S,3S,6R)-2-hydroxy-6-methyl-3-(methylethyl)cyclohexyl methylsulfonate 

Downstream Products

• 102748-64-1 (1R,2S,3S,4S)-2,3-bis-(3,5-dinitro-benzoyloxy)-p-menthane 
• 112506-98-6 (1R,2S,3R,4S)-3-(3,5-dinitro-benzoyloxy)-p-menthan-2-ol 
• 102748-64-1 (1RS,2RS,3SR,4RS)-2,3-bis-(3,5-dinitro-benzoyloxy)-p-menthane 
• 102748-64-1 (1RS,2SR,3SR,4RS)-2,3-bis-(3,5-dinitro-benzoyloxy)-p-menthane 
• 102748-64-1 (1RS,2RS,3RS,4SR)-2,3-bis-(3,5-dinitro-benzoyloxy)-p-menthane 
• 102748-64-1 (1RS,2RS,3RS,4RS)-2,3-bis-(3,5-dinitro-benzoyloxy)-p-menthane 
• 102748-64-1 (1RS,2SR,3SR,4SR)-2,3-bis-(3,5-dinitro-benzoyloxy)-p-menthane 
• 102748-64-1 (1RS,2SR,3RS,4RS)-2,3-bis-(3,5-dinitro-benzoyloxy)-p-menthane 
• 115387-81-0 (1RS,2SR,3RS,4SR)-2,3-bis-(3-nitro-benzoyloxy)-p-menthane 
• 115387-81-0 (1RS,2RS,3SR,4SR)-2,3-bis-(3-nitro-benzoyloxy)-p-menthane 

Relevant articles and documents

Natural-Product-Derived Transient Receptor Potential Melastatin 8 (TRPM8) Channel Modulators

A library of novel structural hybrids of menthol and cubebol was tested for each derivative's ability to interact with the transient receptor potential subfamily melastatin member 8 (TRPM8) channel. This structure-activity relationship study revealed three potent modulators of the TRPM8 ion channel: a novel agonist (4) with an EC50 value of 11 ± 1 μM, an antagonist (15) with an IC50 value of 2 ± 1 μM, and an allosteric modulator (21) that minimized channel desensitization toward menthol. Each of these novel exocyclic olefin analogues of menthol is readily accessible by synthesis and was tested using Ca2+ assays and electrophysiology.

P450 fingerprinting method for rapid discovery of terpene hydroxylating P450 catalysts with diversified regioselectivity

Engineered P450 enzymes constitute attractive catalysts for the selective oxidation of unactivated C-H bonds in complex molecules. A current bottleneck in the use of P450 catalysis for chemical synthesis is the time and effort required to identify the P45

Insight into acid-mediated asymmetric spirocyclization in the presence of a chiral diol

Asymmetric spirocyclization based on intramolecular conjugate addition using a combination of a Lewis acid and an optically active cyclohexane-1,2-diol has been studied in connection with 1) the effect of substituents on the cyclohexane-1,2-diol and 2) th