CAS 105108-20-1

2(3H)-Naphthalenone,4,4a,5,6,7,8-hexahydro-4-hydroxy-1,4a-diméthyl-7-(1-méthyléthényl)-,(4R,4aR,7R)-

Formule : C₁₅H₂₂O₂

InChI : InChI=1S/C15H22O2/c1-9(2)11-5-6-15(4)12(7-11)10(3)13(16)8-14(15)17/h11,14,17H,1,5-8H2,2-4H3/t11-,14-,15-/m1/s1

Code InChI : InChIKey=MROVETGJOLYNJI-KCPJHIHWSA-N

SMILES : C[C@]12C(C[C@H](C(C)=C)CC1)=C(C)C(=O)C[C@H]2O

Synonymes :

• (4R,4aR,7R)-4,4a,5,6,7,8-Hexahydro-4-hydroxy-1,4a-dimethyl-7-(1-methylethenyl)-2(3H)-naphthalenone
• 1b-Hydroxy-a-cyperone
• 2(3H)-Naphthalenone,4,4a,5,6,7,8-hexahydro-4-hydroxy-1,4a-dimethyl-7-(1-methylethenyl)-, [4R-(4a,4aa,7a)]-
• Ligucyperonol
• 2(3H)-Naphthalenone, 4,4a,5,6,7,8-hexahydro-4-hydroxy-1,4a-dimethyl-7-(1-methylethenyl)-, (4R,4aR,7R)-
• (4R)-4,4a,5,6,7,8-Hexahydro-4β-hydroxy-1,4aβ-dimethyl-7β-(1-methylethenyl)naphthalen-2(3H)-one
• (4R)-2,3,4,4a,5,6,7,8-Octahydro-4β-hydroxy-7β-(1-methyleneethyl)-1,4aβ-dimethylnaphthalen-2-one
• 1beta-Hydroxy-alpha-cyperone

Ligucyperonol

CAS : 105108-20-1

Ligucyperonol

Formule : C₁₅H₂₂O₂

Degré de pureté : ≥98%

Masse moléculaire : 234.33

Ref: 54-OR1108295

(4R)-4,4a,5,6,7,8-Hexahydro-4β-hydroxy-1,4aβ-dimethyl-7β-(1-methylethenyl)naphthalen-2(3H)-one

CAS : 105108-20-1

Formule : C₁₅H₂₂O₂

Degré de pureté : 98.0%

Couleur et forme : Solid

Masse moléculaire : 234.3340

Ref: IN-DA0092XT

Ligucyperonol

CAS : 105108-20-1

Ligucyperonol exhibits significant activities on protecting muscle cells from mild to moderate oxidative stress.

Formule : C₁₅H₂₂O₂

Degré de pureté : 98%

Couleur et forme : Solid

Masse moléculaire : 234.33

Ref: TM-TN4438

Ligucyperonol

CAS : 105108-20-1

Formule : C₁₅H₂₂O₂

Degré de pureté : 95%~99%

Masse moléculaire : 234.339

Ref: BP-SBP03288

4-Hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one

CAS : 105108-20-1

4-Hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one is a naturally occurring sesquiterpene, which is a class of terpenes characterized by their 15-carbon skeletons and complex structures. This compound is typically sourced from various plant species known for their volatile oils and resins. Its biosynthesis involves enzymatic reactions that lead to the cyclization and modification of basic isoprene units, often through the action of terpene synthases.

Formule : C₁₅H₂₂O₂

Degré de pureté : Min. 95%

Masse moléculaire : 234.33 g/mol

Ref: 3D-FEA10820