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1(2H)-Naphthalenone, 3,4-dihydro-, hydrazone is a chemical compound with the molecular formula C11H12N2. It is derived from 3,4-dihydro-1(2H)-naphthalenone, which is a reduced form of naphthalenone. The hydrazone functional group is formed by the reaction of the carbonyl group (C=O) with a hydrazine molecule (NH2-NH2), resulting in the formation of a C=N-NH-NH2 structure. 1(2H)-Naphthalenone, 3,4-dihydro-, hydrazone is an organic compound with potential applications in the synthesis of various pharmaceuticals and chemical intermediates. It is important to note that the properties and reactivity of 1(2H)-Naphthalenone, 3,4-dihydro-, hydrazone may vary depending on the specific conditions and reactions it undergoes.

5736-43-6

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5736-43-6 Usage

Synonyms

Tetralone hydrazone, 3,4-dihydro-1(2H)-naphtalene hydrazone

Chemical Structure

A hydrazone derivative of 1(2H)-naphthalenone

Physical State

Yellow to brown solid

Molecular Weight

145.21 g/mol

Appearance

Yellow to brown solid

Potential Applications

a. Nitroso-ruthenium catalyst for the oxidation of alcohols
b. Reagent for the determination of nitrite in water
c. Organic synthesis
d. Building block in the production of pharmaceuticals and agrochemicals

Usage in Research and Industry

Various applications in chemical research and industry, including catalysis and analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 5736-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,3 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5736-43:
(6*5)+(5*7)+(4*3)+(3*6)+(2*4)+(1*3)=106
106 % 10 = 6
So 5736-43-6 is a valid CAS Registry Number.

5736-43-6Relevant academic research and scientific papers

Scalable Wolff-Kishner Reductions in Extreme Process Windows Using a Silicon Carbide Flow Reactor

Znidar, Desiree,O'Kearney-Mcmullan, Anne,Munday, Rachel,Wiles, Charlotte,Poechlauer, Peter,Schmoelzer, Christoph,Dallinger, Doris,Kappe, C. Oliver

, p. 2445 - 2455 (2019)

A safe and scalable continuous flow strategy for Wolff-Kishner reductions that employs methanol as the solvent has been developed. The use of low-cost hydrazine as the reducing agent in combination with a caustic base provides an atom-efficient, environmentally friendly method for the deoxygenation of aldehydes and ketones to alkanes. Because of the required harsh and corrosive reaction conditions (200 °C, 50 bar), reactor materials such as stainless steel, glass, or any type of polymer have compatibility problems, rendering this process problematic on a production scale. The use of corrosion-resistant silicon carbide (SiC) as the reactor material opens up the possibility of performing Wolff-Kishner reductions on scale with a considerably improved safety profile. Methanol as the solvent significantly simplifies the workup procedure compared with the generally employed high-boiling solvents such as diethylene glycol. The continuous flow protocol was applied to a number of substrates and provided the desired products in good to high yields with space-time yields of up to 152 g L-1 h-1. In addition, a pharmaceutically valuable active pharmaceutical ingredient precursor was synthesized by employing this higherature/pressure Wolff-Kishner protocol.

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