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Urea, N-(1-naphthalenylmethyl)-N'-phenyl-, also known as N-(1-naphthylmethyl)-N'-phenylurea or N-(1-naphthalenylmethyl)-N'-phenylurea, is an organic compound with the chemical formula C17H15N2O. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. Urea, N-(1-naphthalenylmethyl)-N'-phenyl- is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its structure consists of a urea core with a naphthalenylmethyl group attached to one nitrogen atom and a phenyl group attached to the other nitrogen atom. The compound is known for its potential applications in the development of new materials and compounds with unique properties, such as luminescent materials and sensors.

92277-89-9

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92277-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92277-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,7 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92277-89:
(7*9)+(6*2)+(5*2)+(4*7)+(3*7)+(2*8)+(1*9)=159
159 % 10 = 9
So 92277-89-9 is a valid CAS Registry Number.

92277-89-9Downstream Products

92277-89-9Relevant academic research and scientific papers

Toward the control of Leptosphaeria maculans: Design, syntheses, biological activity, and metabolism of potential detoxification inhibitors of the crucifer phytoalexin brassinin

Pedras, M. Soledade C.,Jha, Mukund

, p. 4958 - 4979 (2007/10/03)

Brassinin (1), a crucial plant defense produced by crucifers, is detoxified by the phytopathogenic fungus Leptosphaeria maculans (Phoma lingam) to indole-3-carboxaldehyde using a putative brassinin oxidase. Potential inhibitors of brassinin detoxification

ARYLMETHYL ISOCYANATES

Kozhushko, B. N.,Lomakina, A. V.,Paliichuk, Yu. A.,Shokol, V. A.

, p. 654 - 660 (2007/10/02)

Chloromethyl isocyanate reacts readily with aromatic hydrocarbons in the presence of anhydrous ferric chloride or other catalysts of the Friedel-Crafts reaction with the formation of arylmethyl isocyanates.The latter add alcohols and amines readily, being converted into the corresponding substituted urethanes and ureas.When heated in the presence of catalytic amounts of 1,3-dimethylphosphol-3-ene they give substituted carbodiimides.

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