What is the (+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL?

(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL is white solid, while it's Molecular Formula is C10H16O. white solid 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.

What is the CAS number for (+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL?

The CAS number of (+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL is 22972-51-6.

What is the (+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL?

(+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL is white solid, while it's Molecular Formula is C10H16O. white solid 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.

What is the CAS number for (+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL?

The CAS number of (+)-(1S,4R)-P-MENTHA-2,8-DIEN-1-OL is 22972-51-6.

Product classification

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22972-51-6

Product Name:(1S,4R)-1-methyl-4-(prop-1-en-2-yl)cyclohex-2-enol
Molecular Formula:C₁₀H₁₆O
Molecular Weight:152.236
Appearance:white solid

Inquiry

Product Details

Appearance:white solid

Purity:99%

Reliable factory customized supply (1S,4R)-1-methyl-4-(prop-1-en-2-yl)cyclohex-2-enol 22972-51-6

Molecular Formula:C10H16O
Molecular Weight:152.236
Appearance/Colour:white solid
Boiling Point:216.873 °C at 760 mmHg
PKA:14.66±0.40(Predicted)
Flash Point:86.957 °C
PSA：20.23000
Density:0.947 g/cm³
LogP:2.27970

22972-51-6 Relevant articles

Highly efficient catalysts in directed oxygen-transfer processes: Synthesis, structures of novel manganese-containing heteropolyanions, and applications in regioselective epoxidation of dienes with hydrogen peroxide

B?sing, Michael,N?h, Andreas,Loose, Ina,Krebs, Bernt

, p. 7252 - 7259 (1998)

A series of novel manganese(II)-substitu...

Stereoselective Synthesis of Nonpsychotic Natural Cannabidiol and Its Unnatural/Terpenyl/Tail-Modified Analogues

Anand, Radhika,Cham, Pankaj Singh,Gannedi, Veeranjaneyulu,Sharma, Sumit,Kumar, Mukesh,Singh, Rohit,Vishwakarma, Ram A.,Singh, Parvinder Pal

, p. 4489 - 4498 (2022/04/07)

Here, we report a three-step concise and...

Preparation method of (1S, 4R)-1-methyl-4-(1-methylvinyl)-2-cyclohexene-1-ol

-

, (2021/04/17)

The invention relates to a preparation m...

CANNABINOID DERIVATIVES, PRECURSORS AND USES

-

, (2021/03/19)

The present disclosure relates to new ca...

Preparation method of (1S, 4R)-1-methyl-4-(1-methyl vinyl)-2-cyclohexene-1-alcohol

-

, (2021/01/15)

The invention discloses a preparation me...

22972-51-6 Process route

: 5989-27-5,555-08-8,8022-90-0,9003-73-0,95327-98-3
D-limonene

: 99-48-9,1197-06-4,1197-07-5,2102-58-1,2102-59-2,5157-78-8,5503-11-7,7632-16-8,18383-51-2,22567-18-6,20307-86-2
(4R,6R)-carveol

: 18383-51-2,22567-18-6,20307-86-2
(-)-trans-carveol

: 52154-82-2
(1R,4R)-p-mentha-2,8-dien-1-ol

: 22972-51-6
(1S,4R)-p-mentha-2,8-dien-1-ol

: 2102-62-7
p-Menthadiene-<1(7),8>-trans-ol-(2)

: 10374-04-6
p-Menthadiene<1(7),8>-cis-ol-(2)

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane; air; zinc 5,10,15,20-tetraphenylporphyrin; triphenylphosphine; In benzene; for 3h; Irradiation; multistep reaction: photosensitized oxygenation of olefines;
With sodium tetrahydroborate; tetraphenylporphyrine; oxygen; Product distribution; 1.) acetonitrile, irradiation, 2.) methanol; other sensitizers;	40 % Chromat. 9 % Chromat. 16 % Chromat. 7 % Chromat. 23 % Chromat. 5 % Chromat.
With oxygen; fullerene-C₆₀; In toluene; at 0 - 10 ℃; for 4h; Product distribution; Irradiation; other sensitizer in other solvent;

: 1686-14-2,25488-94-2
α-pinene epoxide

: 22771-44-4,3886-78-0,4017-73-6,7212-40-0,22972-51-6,52154-82-2,82769-01-5
(+)-p-mentha-2,8-dien-1-ol

: 4501-58-0,23727-15-3,91200-86-1,91819-58-8
campholenyc aldehyde

: 33171-49-2,56270-99-6,3899-09-0
isocampholenic aldehyde

: 547-61-5,1674-08-4,2158-49-8,3917-59-7,5947-36-4,6712-79-4,19889-99-7,19894-98-5
pinocarveol

: 99-48-9,1197-06-4,1197-07-5,2102-58-1,2102-59-2,5157-78-8,5503-11-7,7632-16-8,18383-51-2,22567-18-6,20307-86-2
(4R,6R)-carveol

: 4017-82-7,52153-53-4,62532-46-1,88390-12-9,103063-10-1,6617-35-2
trans-2-caren-4-ol

Conditions

Conditions	Yield
With Fe/MCM-41(N₂); for 0.166667h;

22972-51-6 Upstream products

138-86-3
limonene.
1686-14-2
α-pinene epoxide
5989-27-5
D-limonene
74756-11-9
(1S,2S,4R)-2-phenylseleninyl-p-menth-8-en-1-ol

22972-51-6 Downstream products

14132-18-4
6,6,9-Trimethyl-3-pentyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromen-1-ol
16849-50-6
tetrahydrocannabinol
111319-95-0
(5R)-2-methyl-5-(1-methylethenyl)-1,3-cyclohexadiene
3901-95-9
cis p-menthanol

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