11056-03-4 Usage
Description
(1R,4aβ)-Decahydro-1β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8aβ-tetramethylnaphthalen-2α-ol is a complex chemical compound belonging to the naphthalenol class. It features a naphthalene ring with a hydroxyl group and a pentenyl chain that includes a double bond, a hydroxyl group, and a methyl group. As a stereoisomer, this compound has a distinct arrangement of carbon atoms, which influences its properties and potential applications.
Uses
Used in Chemical Synthesis:
(1R,4aβ)-Decahydro-1β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8aβ-tetramethylnaphthalen-2α-ol serves as an intermediate or reactant in various chemical synthesis processes. Its unique structure allows it to participate in a range of reactions, making it valuable for creating new compounds with specific properties.
Used in Research:
As a complex and distinctive chemical entity, (1R,4aβ)-Decahydro-1β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8aβ-tetramethylnaphthalen-2α-ol is utilized in research settings to explore its properties, reactivity, and potential interactions with other molecules. This can lead to a better understanding of its behavior and possible applications in different fields.
Used in Pharmaceutical Development:
Due to its unique structure and properties, (1R,4aβ)-Decahydro-1β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8aβ-tetramethylnaphthalen-2α-ol may be investigated for its potential use in pharmaceuticals. It could be studied for its interactions with biological systems, possibly leading to the development of new drugs or therapeutic agents.
Used in Industrial Applications:
(1R,4aβ)-Decahydro-1β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-2,5,5,8aβ-tetramethylnaphthalen-2α-ol's specific configuration and properties may also make it suitable for use in various industrial applications. This could include its use as a component in the development of new materials, coatings, or other products where its chemical characteristics are advantageous.
Check Digit Verification of cas no
The CAS Registry Mumber 11056-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,1,0,5 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 11056-03:
(7*1)+(6*1)+(5*0)+(4*5)+(3*6)+(2*0)+(1*3)=54
54 % 10 = 4
So 11056-03-4 is a valid CAS Registry Number.
11056-03-4Relevant articles and documents
A single residue change leads to a hydroxylated product from the class II diterpene cyclization catalyzed by abietadiene synthase
Criswell, Jared,Potter, Kevin,Shephard, Freya,Beale, Michael H.,Peters, Reuben J.
, p. 5828 - 5831 (2013/02/23)
Class II diterpene cyclases catalyze bicyclization of geranylgeranyl diphosphate. While this reaction typically is terminated via methyl deprotonation to yield copalyl diphosphate, in rare cases hydroxylated bicycles are produced instead. Abietadiene synthase is a bifunctional diterpene cyclase that usually produces a copalyl diphosphate intermediate. Here it is shown that substitution of aspartate for a conserved histidine in the class II active site of abietadiene synthase leads to selective production of 8α-hydroxy-CPP instead, demonstrating striking plasticity.
Oxidative degradation of the sclareol side chain: hemisyntheses of ambergris derivatives using in the key steps palladium complexes or ruthenium tetroxide generated in situ
Zahra, Jean-Pierre,Chauvet, Frederic,Coste-Maniere, Ivan,Martres, Paul,Perfetti, Patricia,Waegell, Bernard
, p. 1001 - 1024 (2007/10/03)
We report the hemisyntheses of various ambergris-type derivatives: ambraoxide 4, Ambrox 8, 13-methylambraoxide 13, ambraketal 14, norambraketal 15, non-norambraketal 16 and dioxepane 53.Sclareol 12 is used as starting material because it is currently available from Salvia sclarea.The key steps involve an oxidative degradation of the sclareol 12 side chain, using either palladium complexes or ruthenium tetroxide generated in situ. - Keywords: sclareol; Ambrox; ambraoxide; 13-methylambraoxide; ambraketal; norambraketal; nor-norambraketal; farnesylic aldehyde; palladium complex; ruthenium tetroxide generated in situ; oxidative degradation
BICYCLIC RESIN ACIDS OF THE OLEORESINS OF Pinus mugo AND P. strobus
Bol'shakova, V. I.,Shmidt, E. N.,Pentegova, V. A.
, p. 260 (2007/10/02)
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