What is the (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene?

(4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene is , while it's Molecular Formula is C 20 H 38 .

What is the CAS number for (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene?

The CAS number of (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene is 561-90-0.

What is (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene (561-90-0) used for?

(4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene is a complex organic compound with a unique molecular structure. It is a decalin derivative, which means it has a decalin ring system, and it is a type of bicyclic compound. The compound is characterized by its stereochemistry, with the 4aR, 5S, 6S, and 8aS configurations indicating the specific arrangement of atoms in three-dimensional space. It features a naphthalene core, which is a hydrocarbon with two fused benzene rings, and is further modified by the presence of methyl groups and a 3-methylpentyl side chain. (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene is an example of the vast diversity in organic chemistry, where small changes in structure can lead to different properties and applications.

What is the (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene?

(4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene is , while it's Molecular Formula is C 20 H 38 .

What is the CAS number for (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene?

The CAS number of (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene is 561-90-0.

What is (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene (561-90-0) used for?

(4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene is a complex organic compound with a unique molecular structure. It is a decalin derivative, which means it has a decalin ring system, and it is a type of bicyclic compound. The compound is characterized by its stereochemistry, with the 4aR, 5S, 6S, and 8aS configurations indicating the specific arrangement of atoms in three-dimensional space. It features a naphthalene core, which is a hydrocarbon with two fused benzene rings, and is further modified by the presence of methyl groups and a 3-methylpentyl side chain. (4aR,5S,6S,8aS)-1,1,4a,6-tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene is an example of the vast diversity in organic chemistry, where small changes in structure can lead to different properties and applications.

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561-90-0

Product Name:15-ol-ent-labdane acid
Molecular Weight:278.5157

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Product Details

Purity:99%

Factory Sells Best Quality 15-ol-ent-labdane acid 561-90-0 with GMP standards

Molecular Formula:C₂₀H₃₈
Molecular Weight:278.5157
Vapor Pressure:0mmHg at 25°C
Boiling Point:332.503°C at 760 mmHg
Flash Point:150.883°C
Density:0.83g/cm³

561-90-0 Process route

: Toluene-4-sulfonic acid (1R,4aR,5S,8aR)-1,4a,6-trimethyl-5-(3-methyl-pentyl)-decahydro-naphthalen-1-ylmethyl ester

: 561-90-0,6868-99-1,95879-87-1,95879-88-2,95879-89-3,95879-98-4
Hexahydrobiformen

Conditions

Conditions	Yield
With lithium aluminium tetrahydride; In 1,4-dioxane; Heating;

: 561-90-0,6868-99-1,95879-87-1,95879-88-2,95879-89-3,95879-98-4
(8S,13Ξ)-Labdan, Hexahydrobiformen, Hexahydrosklaren

Conditions

Conditions	Yield
With hexane; platinum; Hydrogenation_.anschliessend Hydrierung an Palladium/Kohle in Aethanol unter 2 at;
With ethanol; nickel; under 36775.4 Torr; Hydrogenation;

561-90-0 Upstream products

1235-39-8
methyl communate ester

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