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1-Naphthalenecarboxylic acid, 5,6,7,8-tetrahydro-, ethyl ester is a chemical compound with the molecular formula C13H16O2. It is an ester derivative of 1-naphthoic acid, where the 5,6,7,8 positions of the naphthalene ring are fully saturated, and the carboxylic acid group is esterified with ethanol. 1-Naphthalenecarboxylic acid, 5,6,7,8-tetrahydro-, ethyl ester is characterized by its aromatic structure and is used in various applications, such as in the synthesis of pharmaceuticals and other organic compounds. It is an oily liquid with a distinct chemical structure that contributes to its unique properties and reactivity.

4242-17-5

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4242-17-5 Usage

Derived from

1-Naphthalenecarboxylic acid

Type of compound

Ester derivative of naphthalene

Common uses

Intermediate for the synthesis of various pharmaceutical compounds

Potential uses

Treatment of various medical conditions

Different properties

Compared to its parent compound, as an ester

Useful for

Specific applications in the pharmaceutical industry

Check Digit Verification of cas no

The CAS Registry Mumber 4242-17-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,4 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4242-17:
(6*4)+(5*2)+(4*4)+(3*2)+(2*1)+(1*7)=65
65 % 10 = 5
So 4242-17-5 is a valid CAS Registry Number.

4242-17-5Downstream Products

4242-17-5Relevant academic research and scientific papers

Room Temperature Carbonylation of (Hetero) Aryl Pentafluorobenzenesulfonates and Triflates using Palladium-Cobalt Bimetallic Catalyst: Dual Role of Cobalt Carbonyl

Joseph, Jayan T.,Sajith, Ayyiliath M.,Ningegowda, Revanna C.,Shashikanth, Sheena

supporting information, p. 419 - 425 (2017/02/10)

An efficient method for the carbonylation of (hetero) aryl pentafluorobenzenesulfonates and triflates under exceptionally mild conditions using palladium/dicobalt octacarbonyl [Pd/Co2(CO)8] has been developed. Besides acting as carbon monoxide (CO) source, Co2(CO)8enhances the reaction rate by accelerating the CO insertion through an in situ generated bimetallic palladium cobalt tetracarbonyl [Pd-Co(CO)4] complex. Under the optimized reaction condition, carbonylation of a wide range of activated and deactivated, as well as sterically hindered and heteroaromatic, substrates proceeded efficiently at room temperature. The high chemoselectivity and improved synthesis of biologically relevant Isoguvacine and Lazabemide intermediates highlights its scope as a valuable synthetic method. The generality of this protocol was further extended to other electrophiles (bromides, chlorides and tosylates). (Figure presented.).

Quenched skeletal Ni as the effective catalyst for selective partial hydrogenation of polycyclic aromatic hydrocarbons

Liu, Chengyun,Rong, Zeming,Sun, Zhuohua,Wang, Yong,Du, Wenqiang,Wang, Yue,Lu, Lianhai

, p. 23984 - 23988 (2013/11/19)

Quenched skeletal Ni is an active and selective catalyst for selective partial hydrogenation of polycyclic aromatic hydrocarbons (PAHs). The molecular structure of PAHs significantly dominate the hydrogenation process and furthermore, the distribution of hydrogenated products.

Cyclization of benzyne-tethered alkyllithiums: Preparation of 3-substituted benzocyclobutenes and 5-substituted tetralins

Bailey, William F.,Longstaff, Sarah C.

, p. 6899 - 6901 (2007/10/03)

A five-step, one-pot preparation of isomerically pure 3-substituted benzocyclobutenes or 5-substituted tetralins in 20-40% yield from the appropriate α-(2-fluorophenyl)-ω-iodoalkane, involving generation and subsequent 4-or 6-exo cyclization of a benzyne-tethered alkyllithium, is described.

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