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5,6,7,8-tetrahydronaphthalen-2-yl benzoate is a complex organic chemical compound with the molecular formula C17H16O2. It is a derivative of naphthalene, a cyclic aromatic hydrocarbon, and benzoic acid, a carboxylic acid. 5,6,7,8-tetrahydronaphthalen-2-yl benzoate is characterized by a naphthalene ring that has been partially hydrogenated (reduced) to form a tetrahydro structure, and a benzoate group attached to the 2-position of the naphthalene. The benzoate group is an ester derived from benzoic acid and an alcohol, which in this case is part of the tetrahydronaphthalene structure. 5,6,7,8-tetrahydronaphthalen-2-yl benzoate is of interest in organic chemistry and may have applications in the synthesis of various pharmaceuticals and other chemical products due to its unique structure and potential reactivity.

3574-36-5

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3574-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3574-36-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3574-36:
(6*3)+(5*5)+(4*7)+(3*4)+(2*3)+(1*6)=95
95 % 10 = 5
So 3574-36-5 is a valid CAS Registry Number.

3574-36-5Relevant academic research and scientific papers

Acceptorless Dehydrogenation of Hydrocarbons by Noble-Metal-Free Hybrid Catalyst System

Fuse, Hiromu,Kojima, Masahiro,Mitsunuma, Harunobu,Kanai, Motomu

, p. 2042 - 2045 (2018)

A hybrid catalysis that comprises an acridinium photoredox catalyst, a thiophosphate organocatalyst, and a nickel catalyst-enabled acceptorless dehydrogenation of hydrocarbons is reported. The cationic nickel complex played a critical role in the reactivity. This is the first example of acceptorless dehydrogenation of hydrocarbons by base metal catalysis under mild reaction conditions of visible light irradiation at room temperature.

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