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(4aS,6aα,10aβ,10bα)-Dodecahydro-4a,7,7,10a-tetramethyl-3H-naphtho[2,1-b]pyran-3-one is a complex organic compound with a unique molecular structure. It is a dodecahedral hydrocarbon with a naphtho[2,1-b]pyran-3-one core, which is a type of polycyclic aromatic compound. The molecule features a tetramethyl substitution pattern, with four methyl groups attached to the carbon atoms at positions 4a, 7, 7, and 10a. The compound's stereochemistry is defined by the (4aS,6aα,10aβ,10bα) configuration, indicating the specific arrangement of atoms in three-dimensional space. (4aS,6aα,10aβ,10bα)-Dodecahydro-4a,7,7,10a-tetramethyl-3H-naphtho[2,1-b]pyran-3-one is likely to be found in specialized chemical research or industrial applications due to its complex structure and potential for unique chemical properties.

2466-24-2

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2466-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2466-24-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2466-24:
(6*2)+(5*4)+(4*6)+(3*6)+(2*2)+(1*4)=82
82 % 10 = 2
So 2466-24-2 is a valid CAS Registry Number.

2466-24-2Relevant academic research and scientific papers

Total synthesis of (+/-)-syn-copalol.

Toshima, Hiroaki,Oikawa, Hideaki,Yada, Hiroshi,Ono, Hiroshi,Toyomasu, Tomonobu,Sassa, Takeshi

, p. 2504 - 2510 (2007/10/03)

The labdane diterpene derivative, syn-copalol [(+)-5] is the alcohol part of syn-copalyl diphosphate [(+)-4]. In this paper, racemic (+/-)-5 was synthesized from a known racemic lactone in 8 steps. The current and our previous syntheses provide all four copalol derivatives [(+)-3, (-)-3 and (+/-)-5] which are required for the biosynthetic study of polycyclic diterpenes.

New Syntheses of (+/-)-Ambrox, (+/-)-Ambra Oxide and Their Stereoisomers

Kawanobe,Tsuneo,Kogami, Kunio,Matsui, Masanao

, p. 1475 - 1480 (2007/10/02)

New and efficient syntheses of (+/-)-ambrox (1a), (+/-)-ambra oxide (2a) and their stereoisomers (1b, 2b ca. c), amber-like odorous compounds, are described.Starting from dihydro β- and α-ionone (5,12), these substances were obtained in only a few steps via stereoselective acid-catalized cyclization of monocyclodienoic acid (7a ca. b, 11a ca. b, 15a).

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