511-02-4 Usage
Description
Naphthalene, decahydro-1,1, also known as Decahydro-1,1-naphthalene, is a diterpene with a labdane skeleton featuring double bonds at positions C-8(17), C-13(16), and C-14. It is a naturally occurring organic compound derived from the labdane family of diterpenoids.
Uses
Used in Pharmaceutical Industry:
Naphthalene, decahydro-1,1, is used as a pharmaceutical compound for its potential therapeutic properties. Its unique chemical structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs and treatments.
Used in Chemical Industry:
In the chemical industry, naphthalene, decahydro-1,1, is used as a starting material for the synthesis of various chemical products. Its versatile structure can be modified to produce a range of compounds with different applications, such as fragrances, dyes, and other specialty chemicals.
Used in Research and Development:
Naphthalene, decahydro-1,1, is also utilized in research and development for studying the properties and reactivity of labdane-type diterpenoids. This knowledge can be applied to the design and synthesis of novel compounds with potential applications in various fields, including medicine, agriculture, and materials science.
Used in Cosmetics Industry:
Due to its unique chemical structure and properties, naphthalene, decahydro-1,1, can be used as an ingredient in the cosmetics industry. It may be employed in the formulation of fragrances, skincare products, and other personal care items, where its properties can contribute to the product's efficacy and sensory experience.
Check Digit Verification of cas no
The CAS Registry Mumber 511-02-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 511-02:
(5*5)+(4*1)+(3*1)+(2*0)+(1*2)=34
34 % 10 = 4
So 511-02-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H32/c1-7-15(2)9-11-17-16(3)10-12-18-19(4,5)13-8-14-20(17,18)6/h7,17-18H,1-3,8-14H2,4-6H3/t17-,18-,20+/m0/s1
511-02-4Relevant articles and documents
FOLIAGE DITERPENES OF DACRYDIUM INTERMEDIUM: IDENTIFICATION, VARIATION AND BIOSYNTHESIS
Perry, Nigel B.,Weavers, Rex T.
, p. 2899 - 2904 (1985)
The major diterpenes in the foliage of Dacrydium intermedium have been identified as rimuene, ent-rosadiene, ent-beyerene, phyllocladene, ent-kaurene, sclarene and ent-sclarene. ent-Rosadiene and ent-sclarene have not been reported previously from natural sources.Considerable tree-to-tree variations are encountered and genetic control is proposed.Biosynthetic mechanism are put forward to explain the presence of diterpenes of both enantiomeric series.A lack of mono- and sesquiterpenes in both D. intermedium and D. fonkii, which ties in with Quinn's proposed revision of the Dacrydium genus, is also noted.Key Word Index - Dacrydium intermedium; D. fonkii; Podocarpaceae; infraspecific variation; biosynthesis; diterpenes; ent-rosadiene; ent-sclarene; co-occurrence of enantiomers; biochemical systematics; Lepidothamnus.
Development of synthetic routes to D,L-α-tocopherol (vitamin E) from biologically produced geranylgeraniol
Hyatt, John A.,Kottas, Gregg S.,Effler, Janet
, p. 782 - 787 (2013/09/06)
The use of the biologically derived diterpene alcohol geranylgeraniol was explored as an alternative to petrochemical-based isophytol as a side-chain synthon for producing D,L-α-tocopherol. Two routes were studied, both of which begin with allylic epoxidation followed by olefin hydrogenation to give epoxyphytol. Epoxyphytol can be reduced with Red-Al to provide phytan-1,3-diol which upon acid-catalyzed condensation with trimethylhydroquinone gives vitamin E in fair yield. In a higher-yielding process, epoxyphytol was deoxygenated with methylrhenium trioxide/triphenylphosphine to generate a mixture of phytol and isophytol (> 90% yield from geranylgeraniol). This mixture can serve as a "plug-in" replacement for isophytol in the final step of the currently practiced vitamin E chemistry. The use of methylrhenium trioxide to catalyse dehydration of vinyl dialkyl carbinols to 1,3-dienes was also demonstrated.
