CAS 55881-96-4

Decahydro-2-hydroxy-2,5,5,8a-tetramethyl-1-naphthaleneethanol

Description:

Decahydro-2-hydroxy-2,5,5,8a-tetramethyl-1-naphthaleneethanol, identified by its CAS number 55881-96-4, is an organic compound characterized by its complex structure, which includes a naphthalene ring system that has been saturated and functionalized. This compound features a hydroxyl (-OH) group, contributing to its classification as an alcohol. The presence of multiple methyl groups indicates that it is a highly branched molecule, which can influence its physical properties such as boiling point, solubility, and volatility. Typically, compounds of this nature exhibit hydrophobic characteristics due to their large hydrocarbon framework, while the hydroxyl group can impart some degree of hydrophilicity. This substance may be utilized in various applications, including as a fragrance or flavoring agent, owing to its pleasant odor profile. Additionally, its structural features suggest potential uses in the synthesis of more complex organic molecules or as an intermediate in chemical manufacturing. Safety data and handling precautions should be consulted, as with all chemical substances, to ensure proper usage and risk management.

Formula: C₁₆H₃₀O₂

InChI: InChI=1/C16H30O2/c1-14(2)8-5-9-15(3)12(14)6-10-16(4,18)13(15)7-11-17/h12-13,17-18H,5-11H2,1-4H3

InChI key: InChIKey=AIALTZSQORJYNJ-UHFFFAOYSA-N

SMILES: CC12C(CCC(C)(O)C1CCO)C(C)(C)CCC2

Synonyms:

• 1-(2-Hydroxyethyl)-2,5,5,8A-Tetramethyldecahydronaphthalen-2-Ol
• 1-(2-Hydroxyethyl)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol
• 1-Naphthaleneethanol, decahydro-2-hydroxy-2,5,5,8a-tetramethyl-
• Decahydro-2-hydroxy-2,5,5,8a-tetramethyl-1-naphthaleneethanol
• Sclareol glycol
• beta-(2-Hydroxy-2,5,5,9-tetramethyldecalyl) ethanol
• Decahydro-2-hydroxy-2,5,5,8a-tetramethylnaphthalene-1-ethanol
• Einecs 259-880-1
• (1R,4aα)-Decahydro-2α-hydroxy-2,5,5,8aβ-tetramethyl-1-naphthaleneethanol
• Sclareol GlycoI
• 2-Hydroxy-1-(2-hydroxyethyl)-2,5,5,8a-tetramethyldecahydronaphthalene

1-Naphthaleneethanol, decahydro-2-hydroxy-2,5,5,8a-tetramethyl-

CAS: 55881-96-4

Formula: C₁₆H₃₀O₂

Purity: %

Color and Shape: Solid

Molecular weight: 254.4082

Ref: IN-DA00I9Z8

Sclareol glycol

CAS: 55881-96-4

Formula: C₁₆H₃₀O₂

Molecular weight: 254.41

Ref: 7W-GY2312

Sclareol glycol, 10mM (in DMSO)

CAS: 55881-96-4

Sclareol glycol, 10mM (in DMSO)

Purity: ≥98%

Molecular weight: 254.41g/mol

Ref: 54-BUP19579

Sclareol glycol

CAS: 55881-96-4

Formula: C₁₆H₃₀O₂

Purity: 95%~99%

Molecular weight: 254.41

Ref: BP-BP3935

Sclareol glycol

CAS: 55881-96-4

Sclareol glycol is the precursor of ambroxide.

Formula: C₁₆H₃₀O₂

Purity: 98% - 99.87%

Color and Shape: Solid

Molecular weight: 254.41

Ref: TM-T8295

Sclareol Glycol

CAS: 55881-96-4

Applications Sclareol Glycol is a reversible activator of adenylate cyclase sclareol glycol (SG), a semisynthetic diterpene of the labdane family. Anti-hypoxia agent.
References Georgieva J. et al.: Methods Find. Exp. Clin. Pharmacol., 12, 591 (1990);

Formula: C₁₆H₃₀O₂

Color and Shape: Neat

Molecular weight: 254.41

Ref: TR-S199895

Sclareol Glycol

Controlled Product

CAS: 55881-96-4

Sclareol glycol is a natural product that has been shown to have a variety of physiological effects. It is a carbon source for bacteria and yeast. Sclareol glycol also stimulates the release of extracellular calcium (Ca2+) in tissue cultures, which may be due to its ability to stimulate cytosolic Ca2+ levels. In addition, sclareol glycol has been shown to increase renal blood flow and inhibit the synthesis of dopamine by inhibiting translation in kidney cells. Sclareol glycol also induces locomotor activity in mice, likely through its ability to bind with GABA receptors in the brain.

Formula: C₁₆H₃₀O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 254.41 g/mol

Ref: 3D-FCA88196