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Naphthalene, 1,4-dihydro-5,8-dimethyl-, also known as 5,8-dimethyl-1,4-naphthoquinone or menadione, is an organic compound with the chemical formula C11H10O2. It is a yellow crystalline solid that is soluble in organic solvents and slightly soluble in water. Menadione is a synthetic analog of vitamin K3 and is used as a vitamin supplement, particularly in animal feed. It is also employed as a redox indicator in titrations and as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its potential toxicity and ability to induce oxidative stress, menadione is classified as a hazardous substance and requires proper handling and disposal.

2717-33-1

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2717-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2717-33-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2717-33:
(6*2)+(5*7)+(4*1)+(3*7)+(2*3)+(1*3)=81
81 % 10 = 1
So 2717-33-1 is a valid CAS Registry Number.

2717-33-1Downstream Products

2717-33-1Relevant academic research and scientific papers

Competition between Birch Reduction and Bond Cleavage in 1,2-Bis(4-methyl-1-naphthyl)ethane

Marcinow, Zbigniew,Hull, C. Eugene,Rabideau, Peter W.

, p. 3602 - 3605 (2007/10/02)

The reaction of 1,2-bis(4-methyl-1-naphthyl)ethane with Li, Na, and K in ammonia, THF, and HMPA, or mixtures thereof, has been examined with respect to the factors favoring Birch reduction of the aromatic ring and cleavage of the ethane carbon-carbon bond.Bond cleavage was found to increase relative to ring reduction in the series Li Na K and with the solvents NH3 THF HMPA.However, the latter position of ammonia may be due to the necessarily restricted low-reaction temperature since only ring reduction was observed at temperatures at or below the boiling pointof ammonia (-33 deg C).A number of reduction and cleavage products were isolated and identified, and the mechanistic pathways for their formation is discussed.

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