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7-methoxy-1,1,4aβ-trimethyl-1,2,3,4,4aβ,9,10,10aβ-octahydrophenanthrene is a complex organic compound belonging to the phenanthrene family. It is characterized by a phenanthrene core, which is a tricyclic aromatic hydrocarbon, with a methyl group at positions 1 and 4aβ, and a methoxy group at position 7. The compound also features a saturated octahydro ring system, which contributes to its unique chemical properties. This molecule is of interest in the field of organic chemistry, particularly in the synthesis of natural products and pharmaceuticals, due to its potential applications in the development of new drugs and other chemical compounds.

1730-51-4

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1730-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1730-51-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1730-51:
(6*1)+(5*7)+(4*3)+(3*0)+(2*5)+(1*1)=64
64 % 10 = 4
So 1730-51-4 is a valid CAS Registry Number.

1730-51-4Downstream Products

1730-51-4Relevant academic research and scientific papers

Stereoselective intramolecular 6-exo-Heck reaction : A facile synthetic route to podocarpa-8,11,13-triene and diterpenoid resin acids intermediates

Mukhopadhyaya, Jayanta K.,Ghosh, Ajit K.,Ghatak, Usha Ranjan

, p. 835 - 837 (2007/10/03)

Intramolecular Heck reaction of the olefins 1a-c in the presence of sodium formate affords ca 3:1 mixtures of the respective trans- and cis-octahydrophenanthrenes 3a-c and 4a-c. Similar reaction of the olefmic ester 2 provides a 70:30 mixture of (±)-methyl desisopropyldehydroabietate 6 and (±)10-epi-methyl desoxypodocarpate 7.

Diterpene Synthesis.III. Acid-Catalyzed Cyclization of Methoxy-phenylethyltrimethyl-cyclohexanols, -cyclohexenols and -cyclohexenones

Davis, Brian R.,Hinds, Mark G.,Johnson, Stephen J.

, p. 1815 - 1825 (2007/10/02)

Cyclization of the methoxyphenylethyltrimethylcyclohexanols (3), (4) and (5), the cyclohexenols (6) and (7) and the cyclohexenones (20) and (21), in presence of a variety of acids, has been studied and the products analysed by chromatographic and spectros

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