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1,4-Methanoazulen-7(1H)-one, octahydro-1,5,5,8a-tetramethyl-, (1S,3aR,4S,8aS)- (8CI,9CI) is a complex organic compound with the molecular formula C13H22O. It is a derivative of the azulen-7(1H)-one structure, featuring a methane bridge connecting the 1 and 4 positions. The compound is characterized by its octahydro structure, indicating the presence of eight hydrogen atoms in a cyclic structure. The tetramethyl groups are located at positions 1, 5, 5, and 8a, and the compound has a specific chiral configuration, with the 1S, 3aR, 4S, and 8aS stereochemistry. 1,4-Methanoazulen-7(1H)-one,octahydro-1,5,5,8a-tetramethyl-, (1S,3aR,4S,8aS)- (8CI,9CI) is likely to be found in the chemical industry, potentially used in the synthesis of various pharmaceuticals, fragrances, or other specialty chemicals due to its unique structure and properties.

26804-56-8

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26804-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26804-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,8,0 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26804-56:
(7*2)+(6*6)+(5*8)+(4*0)+(3*4)+(2*5)+(1*6)=118
118 % 10 = 8
So 26804-56-8 is a valid CAS Registry Number.

26804-56-8Upstream product

26804-56-8Relevant academic research and scientific papers

TERPENOIDS. CONDENSATION PRODUCTS OF LONGIFOLENE AND PHENOL

PATNEKAR SG,BHATTACHARYYA SC

, p. 36 - 39 (2007/10/13)

The condensation of longifolene with phenol in the presence of BF//3-etherate at 0 C affords a mixture of two longibornyl phenyl ethers, the structures of which and also of the isobornyl phenyl ether, obtained by a similar reaction from camphene, have been established by their stereospecific cleavage to the known alcohols with li-liquid ammonia. The condensation of longifolene with phenol at 100 C leads to the formation of terpenyl phenois of undecided structures.

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