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Postion:Product Catalog >Organic Chemistry>Alcohols,Phenols,Phenol alcohols>(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL
(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL
  • (+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL

(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL

Price $7
Package 1KG
Min. Order: 1KG
Supply Ability: 1000KGS
Update Time: 2024-08-15

Product Details

Product Name: (+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL CAS No.: 22972-51-6
Min. Order: 1KG Purity: 98%
Supply Ability: 1000KGS Release date: 2024/08/15

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(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL Basic information
Product Name:(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL
Synonyms:(1S,4R) 1-METHYL-4-(1-METHYLETHENYL)-2-CYCLOHEXEN-1-OL;(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL;2-Cyclohexen-1-ol,1-Methyl-4-(1-Methylethenyl)-, (1S,4R)-;(1S,4R)-1-methyl-4-prop-1-en-2-ylcyclohex-2-en-1-ol;(1S,4R)-p-Menth-2,8-dien-1-ol;(1S,4S)-1-methyl-4-(prop-1-en-2-yl)cyclohex-2-en-1-ol;(1S,4R)-1-methyl-4-(prop-1-en-2-yl)cyclohex-2-en-1-ol22972-51-6;(1S,4R)-1-methyl-4-(prop-1-en-2-yl)cyclohex-2-enol
CAS:22972-51-6
MF:C10H16O
MW:152.23
EINECS:805-440-4
Product Categories:
Mol File:22972-51-6.mol
Article illustration


(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL Chemical Properties
Boiling point 69-70 °C(Press: 3 Torr)
density 0.9398
storage temp. 2-8°C
solubility Chloroform (Soluble), Methanol (Soluble)
pka14.66±0.40(Predicted)
form Oil
color Colourless
Water Solubility 4.2g/L
Stability:Light Sensitive
InChIInChI=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
InChIKeyMKPMHJQMNACGDI-VHSXEESVSA-N
SMILES[C@@]1(C)(O)CC[C@@H](C(C)=C)C=C1
LogP2.82


Safety Information
HS Code 2906190090
MSDS Information


(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL Usage And Synthesis
Uses(+)-(1S,4R)-P-MENTHA-2,8-DIEN-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.
Uses1-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.




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