468-84-8 Usage
Description
[4aR-(4aalpha,6abeta,10aalpha,10bbeta)]-dodecahydro-4a,7,7,10a-tetramethyl-3H-naphth[2,1-b]pyran-3-one, commonly known as djson, is a complex chemical compound belonging to the class of naphthopyrans. It is a tetramethylated derivative of dodecahydronaphthalene, which contributes to its unique molecular structure. Djson has been the subject of research due to its potential therapeutic properties, such as acting as an anti-inflammatory, analgesic, antioxidant, and possibly providing neuroprotective effects.
Uses
Used in Pharmaceutical Applications:
Djson is used as a therapeutic agent for its potential anti-inflammatory and analgesic properties, which can be beneficial in the treatment of various conditions characterized by inflammation and pain.
Used in Antioxidant Applications:
As an antioxidant, djson is used to protect cells from oxidative stress and damage, which can be helpful in preventing or treating a range of diseases associated with oxidative stress, such as neurodegenerative disorders.
Used in Neuroprotective Applications:
Djson's potential neuroprotective effects make it a candidate for use in applications aimed at protecting the nervous system and preventing neurodegenerative diseases.
Used in Research and Development:
Due to its ongoing research and exploration of biological activities, djson is used in the field of research and development to further understand its potential applications in medicine and other fields.
Used in Cosmetics Industry:
Given its anti-inflammatory and antioxidant properties, djson may also find applications in the cosmetics industry for the development of products aimed at skin health and protection.
Check Digit Verification of cas no
The CAS Registry Mumber 468-84-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 468-84:
(5*4)+(4*6)+(3*8)+(2*8)+(1*4)=88
88 % 10 = 8
So 468-84-8 is a valid CAS Registry Number.
468-84-8Relevant articles and documents
PRODUCTS OF THE OZONOLYSIS OF ISOABIENOL
Aryku, A. N.,Mironov, G. N.,Koltsa, M. N.,Vlad, P. F.
, p. 42 - 45 (1991)
The ozonization of abienol in ethyl acetate in the presence of pyridine or in methanol followed by the reduction of the peroxides by methyl sulfide has given ambreinolide.On reduction of the peroxide products of the ozonolysis of isoabienol in methanol with potassium tetrahydroborate, the main reaction product was 15,16-bisnorlabdane-8,13,14-triol.Dimethyl sulfide first caused the rearrangement of the peroxide products of ozonization with the cleavage of the ordinary C-13-C-14 carbon bond, and then their reduction.
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Lederer,Stoll
, p. 1345,1347 (1950)
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New total synthesis of (+)-ambrein
Fujiwara, Naoko,Kinoshita, Masako,Akita, Hiroyuki
, p. 3037 - 3045 (2007/10/03)
The convergent synthesis of (+)-ambrein 1 was achieved based on a modified Julia coupling reaction between aldehyde 14 corresponding to the left-half A and sulfone 25a or 25b corresponding to the right-half B. Aldehyde 14 was synthesized in 14% overall yield (nine steps) from the enzymatic resolution product, epoxy alcohol (8aS)-2. Sulfone 25a or 25b was synthesized in 11 steps (25a: 41% overall yield, 25b: 56% overall yield) from the enzymatic resolution product, (1S,6S)-2,2-dimethyl-6-hydroxyhexane-1-carboxylate 4.
Cloning and functional expression of cDNA encoding aphidicolan-16β-ol synthase: A key enzyme responsible for formation of an unusual diterpene skeleton in biosynthesis of aphidicolin
Oikawa,Toyomasu,Toshima,Ohashi,Kawaide,Kamiya,Ohtsuka,Shinoda,Mitsuhashi,Sassa
, p. 5154 - 5155 (2007/10/03)
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