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(3R,4aR,5S,6R,8aR)-5-(2-Furan-3-yl-ethyl)-3-hydroxy-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester is a complex terpenoid compound derived from a naphthalene core. It features a methyl ester group, a hydroxyl group, and multiple methyl groups attached to the naphthalene ring, along with a furan-ethyl side chain. The molecule is characterized by the presence of multiple chiral centers, which contribute to its unique stereochemistry. (3R,4aR,5S,6R,8aR)-5-(2-Furan-3-yl-ethyl)-3-hydroxy-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester may hold potential for applications in the pharmaceutical or chemical industries due to its intricate structure and possible bioactivity, although further research is required to explore its properties and uses.

50428-93-8

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50428-93-8 Usage

Uses

Used in Pharmaceutical Industry:
(3R,4aR,5S,6R,8aR)-5-(2-Furan-3-yl-ethyl)-3-hydroxy-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester is used as a potential pharmaceutical agent for its possible bioactivity and complex structure. (3R,4aR,5S,6R,8aR)-5-(2-Furan-3-yl-ethyl)-3-hydroxy-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester's multiple chiral centers and functional groups may contribute to its interaction with biological targets, making it a candidate for drug development.
Used in Chemical Industry:
In the chemical industry, (3R,4aR,5S,6R,8aR)-5-(2-Furan-3-yl-ethyl)-3-hydroxy-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester may be utilized as a precursor or intermediate in the synthesis of other complex organic compounds. Its unique structure and functional groups could be leveraged to create novel chemical entities with specific applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 50428-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,2 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50428-93:
(7*5)+(6*0)+(5*4)+(4*2)+(3*8)+(2*9)+(1*3)=108
108 % 10 = 8
So 50428-93-8 is a valid CAS Registry Number.

50428-93-8Downstream Products

50428-93-8Relevant academic research and scientific papers

STEREOCHEMISTRY OF STRICTIC ACID AND RELATED FURANODITERPENES FROM CONYZA JAPONICA AND GRANGEA MADERASPATANA

Pandey, Umesh C.,Singhal, Ashok K.,Barua, Nabin C.,Sharma, R. P.,Baruah, Jogendra N.,et al.

, p. 391 - 398 (2007/10/02)

Extraction of Conyza japonica gave strictic acid, ent-2β-hydroxy-15,16-epoxy-3,13(16),14-clerodatrien-18-oic acid and 5,7-dihydroxy-3,8,4'-trimethoxyflavone.Extraction of Grangea maderaspatana gave (-)-hardwickiic acid, ent-15,16-epoxy-1,3,13(16),14-clerodatetraen-18-oic acid and 3-hydroxy-8-acetoxypentadeca-1,9,14-trien-4,6-diyne.The structure of ent-2β-hydroxy-15,16-epoxy-3,13(16),14-clerodatrien-18-oic acid was deduced by spectroscopic methods and by partial synthesis from (-)-hardwickiic acid and the stereochemistries of strictic acid and ent-15,16-epoxy-1,3,13(16),14-clerodatetraen-18-oic acid were established by correlation with ent-2β-hydroxy-15,16-epoxy-3,13(16),14-clerodatrien-18-oic acid. - Keywords: Conyza japonica; Grangea maderaspatana; Compositae; Astereae; strictic acid; clerodanes; 5,7-dihydroxy-3,8,4'-trimethoxyflavone; 3-hydroxy-8-acetoxy-pentadeca-1,9,14-trien-4,6-diyne.

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