CAS 22972-51-6
:(1S,4R)-1-Methyl-4-(1-methylethenyl)-2-cyclohexen-1-ol
Description:
(1S,4R)-1-Methyl-4-(1-methylethenyl)-2-cyclohexen-1-ol, with the CAS number 22972-51-6, is a bicyclic organic compound characterized by its unique structure that includes a cyclohexene ring with various substituents. This compound features a hydroxyl group (-OH) that contributes to its reactivity and potential as an alcohol. The presence of a methyl group and a methylethenyl group indicates that it has branched alkyl substituents, which can influence its physical properties, such as boiling point and solubility. The stereochemistry denoted by (1S,4R) suggests specific spatial arrangements of its atoms, which can affect its biological activity and interactions with other molecules. Typically, compounds like this may exhibit interesting properties such as fragrance or flavor characteristics, making them relevant in the fields of perfumery and food science. Additionally, the compound may participate in various chemical reactions, including oxidation and substitution, due to the presence of the hydroxyl group and the unsaturation in the cyclohexene ring.
Formula:C10H16O
InChI:InChI=1S/C10H16O/c1-8(2)9-4-6-10(3,11)7-5-9/h4,6,9,11H,1,5,7H2,2-3H3/t9-,10+/m0/s1
InChI key:InChIKey=MKPMHJQMNACGDI-VHSXEESVSA-N
SMILES:C(C)(=C)[C@@H]1CC[C@](C)(O)C=C1
Synonyms:- (+)-(1S,4R)-p-Mentha-2,8-dien-1-ol
- (+)-cis-p-Mentha-2,8-dien-1-ol
- (+)-p-Mentha-2,8-dien-1-ol
- (1S,4R)-1-Methyl-4-(1-methylethenyl)-2-cyclohexen-1-ol
- (1S,4R)-1-Methyl-4-(Prop-1-En-2-Yl)Cyclohex-2-Enol
- (1S,4R)-p-Menth-2,8-dien-1-ol
- 2-Cyclohexen-1-ol,1-methyl-4-(1-methylethenyl)-, (1S-cis)-
- cis-Isolimonenol
- p-Mentha-2,8-dien-1-b-ol
- p-Mentha-2,8-dien-1-ol, stereoisomer
- 2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethenyl)-, (1S,4R)-
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Found 9 products.
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethenyl)-, (1S,4R)-
CAS:Formula:C10H16OPurity:97%Color and Shape:LiquidMolecular weight:152.2334Ref: IN-DA002LQK
1g20.00€5g50.00€10g71.00€25g111.00€50g155.00€100g270.00€500gTo inquire250mgTo inquire(+)-p-Mentha-2,8-dien-1-ol, 98%
CAS:Formula:C10H16OPurity:≥ 90.0%Color and Shape:Clear, colourless to light-yellow liquidMolecular weight:152.23(+)-p-Mentha-2,8-dien-1-ol, 95%
CAS:Formula:C10H16OPurity:≥ 95.0%Color and Shape:Clear, colourless to light-yellow liquidMolecular weight:152.23(1S,4R)-1-Methyl-4-(prop-1-en-2-yl)cyclohex-2-en-1-ol
CAS:(1S,4R)-1-Methyl-4-(prop-1-en-2-yl)cyclohex-2-en-1-olFormula:C10H16OPurity:98%Color and Shape: clear. faint yellow liquidMolecular weight:152.23g/mol(1S,4R)-4-Isopropenyl-1-methylcyclohex-2-en-1-ol
CAS:Formula:C10H16OPurity:97%Color and Shape:Liquid, ClearMolecular weight:152.237cis-Isolimonenol
CAS:<p>cis-Isolimonenol is a natural terpenoid alcohol suitable for biochemical experiments and drug synthesis research.</p>Formula:C10H16OPurity:97.30%Color and Shape:SolidMolecular weight:152.23(1S,4R)-4-Isopropenyl-1-methylcyclohex-2-en-1-ol
CAS:<p>(1S,4R)-4-Isopropenyl-1-methylcyclohex-2-en-1-ol is an organic compound that belongs to the group of flavouring agents. It is a multistep synthesis from cyclohexene, which involves isomerization and diastereoisomeric rearrangement. The intermediate in this process is an acid catalyst, which can be obtained by oxidation of alcohols. This process yields high yields of the desired product with byproducts such as alcohols and hydrocarbons in small quantities.</p>Formula:C10H16OPurity:Min. 98 Area-%Color and Shape:Colorless Clear LiquidMolecular weight:152.23 g/mol(1S,4R)-1-Methyl-4-(1-methylethenyl)-2-cyclohexen-1-ol
CAS:Controlled Product<p>Applications 1-Methyl-4-(1-methylethenyl)-2-cyclohexen-1-ol is an acetal reagent used in the synthesis of desoxy cannabidiols and THC (T293202) related psychoactive compounds. It is formed from (+)-Limonene using a photosynthesized O2 transfer.<br>References Wilkinson, S. et al.: Tetrahedron Lett., 54, 52 (2013);<br></p>Formula:C10H16OColor and Shape:NeatMolecular weight:152.23







