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N-(naphthalen-1-yl)naphthalene-1-carboxamide is an organic compound with the molecular formula C20H15NO. It is a white crystalline solid that is soluble in organic solvents. N-(naphthalen-1-yl)naphthalene-1-carboxamide is characterized by its two naphthalene rings, one of which is connected to an amide group. The naphthalene rings are fused, with the amide group attached to the first ring. This structure gives the compound unique chemical and physical properties, making it a potential candidate for various applications in the fields of chemistry and materials science.

5439-52-1

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5439-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5439-52-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5439-52:
(6*5)+(5*4)+(4*3)+(3*9)+(2*5)+(1*2)=101
101 % 10 = 1
So 5439-52-1 is a valid CAS Registry Number.

5439-52-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-<1>Decahydrochinolylmethyl-succinimid

1.2 Other means of identification

Product number -
Other names N-(1-naphthyl)-1-naphthalenecarboxamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5439-52-1 SDS

5439-52-1Downstream Products

5439-52-1Relevant academic research and scientific papers

Experiments Towards the Preparation of Some Binaphthalene Derivatives

Bradshaw, Jerald S.,Golic, Ljubo,Tisler, Miha

, p. 327 - 332 (1988)

Oxidative dimerization of some naphthalene derivatives were studied.With vanadium oxytrichloride either a new C-C bond formation occured or the reagent caused chlorination of the ring.Attempts to induce photochemically a new C-C bond failed. - Keywords: Cyclization; C-C bond formation; Substituted naphthalenes

Palladium-Catalyzed Annulation of Arylbenzamides with Diaryliodonium Salts

Pan, Cheng,Wang, Limin,Han, Jianwei

supporting information, p. 268 - 273 (2021/11/09)

By using diaryliodonium salts, a cylization has been accomplished in the synthesis of N-aryl phenanthridinone derivatives via a cascade of ortho-arylation and Csp2-N bond formation in the presence of palladium catalyst. The reaction exhibits a broad compatibility of readily available N-arylnaphthamides. (Figure presented.).

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