55881-96-4 Usage
Description
Decahydro-2-hydroxy-2,5,5,8a-tetramethylnaphthalene-1-ethanol is a complex organic compound with a unique molecular structure. It is characterized by its decahydronaphtalene core, which consists of a naphthalene ring fused with a cyclohexane ring, and features a hydroxyl group and an ethanol side chain. decahydro-2-hydroxy-2,5,5,8a-tetramethylnaphthalene-1-ethanol is known for its diverse applications across various industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
Decahydro-2-hydroxy-2,5,5,8a-tetramethylnaphthalene-1-ethanol is used as a pharmaceutical compound for its potential therapeutic applications. Its unique structure allows it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Synthesis:
In the field of chemical synthesis, decahydro-2-hydroxy-2,5,5,8a-tetramethylnaphthalene-1-ethanol serves as a key intermediate or building block for the creation of more complex molecules. Its versatile structure can be further modified to produce a range of valuable compounds.
Used in Cosmetics Industry:
Decahydro-2-hydroxy-2,5,5,8a-tetramethylnaphthalene-1-ethanol is used as an active ingredient in the cosmetics industry, where it may be employed for its potential skin care benefits. Its unique properties could contribute to the development of innovative cosmetic products.
Used in Research and Development:
decahydro-2-hydroxy-2,5,5,8a-tetramethylnaphthalene-1-ethanol is also used in research and development settings, where it can be studied for its potential applications in various fields. Its unique structure and properties make it an interesting subject for scientific investigation.
Used in Anti-hypoxia Applications:
Decahydro-2-hydroxy-2,5,5,8a-tetramethylnaphthalene-1-ethanol is used as an anti-hypoxia agent, particularly in the development of drugs that can help improve oxygen delivery and utilization in the body. Its unique properties may contribute to the enhancement of cellular respiration and energy production under low-oxygen conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 55881-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,8 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55881-96:
(7*5)+(6*5)+(5*8)+(4*8)+(3*1)+(2*9)+(1*6)=164
164 % 10 = 4
So 55881-96-4 is a valid CAS Registry Number.
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
55881-96-4Relevant articles and documents
METHOD FOR PRODUCING N,N-DIALKYLHOMOFARNESIC ACID AMIDE
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, (2015/09/23)
Provided are: a method for producing N,N-dialkylhomofarnesic acid amide, which is a precursor of (±)-3a,6,6,9a-tetramethyldodecahydronaphtho[2.1-b]furan that is useful as a fragrance, at a high recovery rate of a raw material, at a high purity and at a high yield; and a method for producing (±)-3a,6,6,9a-tetramethyldodecahydronaphtho[2.1-b]furan. It is a method for producing N,N-dialkylhomofarnesic acid amide, said method including reacting nerolidol with N,N-dialkylformamide dimethyl acetal under the conditions that the N,N-dialkylformamide dimethyl acetal can be refluxed, wherein the molar ratio of the N,N-dialkylformamide dimethyl acetal to the nerolidol is in a range of 1.5 to 3.
PROCESS FOR PRODUCTION OF (±)-3a,6,6,9a TETRAMETHYLDECAHYDRONAPHTHO[2,1-b]FURAN-2(1H)-ONE
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Page/Page column 10; 12, (2009/05/29)
The present invention relates to industrially useful production processes in which (±)-3a,6,6,9a-tetramethyldecahydronaphtho[2,1-b]furan-2(1H)-ones and further (±)-3a,6,6,9a-tetramethyldo decahydronapbtho[2,1-b]furans are produced from raw materials which are readily available at low costs, through short steps and in a simple manner. The process for producing (±)-3a,6,6,9a-tetramethyldecahydronaphtho[2,1-b]furan-2(1H)-ones represented by the general formula (III): which includes the steps of cyclizing a homofarnesylic acid amide represented by the general formula (I): wherein R1 and R2 are each independently an alkyl group having 1 to 4 carbon atoms; and wavy lines each represents a carbon-to-carbon single bond having a cis or trans structure, and/or a monocyclohomofarnesylic acid amide represented by the general formula (II): wherein R1 and R2 and wavy lines are the same as defined above; and dotted lines represent that a carbon-to-carbon double bond is present at any of positions represented by the dotted lines, in the presence off an acid agent; and subjecting the cyclized product to hydrolysis.
Ambergris compounds from labdanolic acid
Urones,Basabe,Marcos,Gonzalez,Jimenez,Sexmero,Lithgow
, p. 9991 - 9998 (2007/10/02)
Labdanolic acid (Cistus ladaniferus) is transformed into derivatives with amber odor. The strategy used allowed a process in which the oxidative decarboxylation reaction was carried out with the hydroxyl group protected.
