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1-Hydroxy-4-prenylnaphthalene is a naturally occurring organic compound characterized by a naphthalene core, which is a bicyclic aromatic hydrocarbon. This specific compound features a hydroxyl group (-OH) at the 1st position and a prenyl group (a C5H9 unit derived from isoprene) attached at the 4th position. It is known for its presence in various plants and has been studied for its potential biological activities, such as antioxidant properties and possible roles in plant defense mechanisms. The prenylation of the naphthalene ring in 1-hydroxy-4-prenylnaphthalene contributes to its unique chemical reactivity and may influence its interactions within biological systems.

2960-04-5

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2960-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2960-04-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2960-04:
(6*2)+(5*9)+(4*6)+(3*0)+(2*0)+(1*4)=85
85 % 10 = 5
So 2960-04-5 is a valid CAS Registry Number.

2960-04-5Downstream Products

2960-04-5Relevant academic research and scientific papers

TWO NAPHTHOPYRAN DERIVATIVES FROM FARAMEA CYANEA

Ferrari, F.,Monache, G. Delle,Lima, R. Alves

, p. 2753 - 2755 (1985)

Four anthraquinones and two new products, faramol (3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-naphthopyran) and 7-methoxyfaramol (3,4-dihydro-3-hydroxy-7-methoxy-2,2-dimethyl-2H-naphthopyran), have been isolated from Faramea cyanea. Key Word Index - Faramea cyanea; Rubiaceae; naphthopyrans; anthraquinones; lichexanthone.

Water-Accelerated Claisen Rearrangements

Wipf, Peter,Rodriguez, Sonia

, p. 434 - 440 (2007/10/03)

Allyl aryl ethers undergo accelerated Claisen and [1,3] rearrangements in the presence of a mixture of trialkylalanes and water or aluminoxanes. The ratio of ortho-, meta-, and pora-Claisen products depends to a large extent on the presence of water and to a much lesser extent on the nature of the alane.

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