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2,3,4-Triphenyl-1-naphthol is a complex organic compound characterized by its unique molecular structure, which consists of a naphthalene core with three phenyl rings attached at the 2nd, 3rd, and 4th positions. 2,3,4-triphenyl-1-naphthol is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its ability to form stable complexes and its optical properties. It is also recognized for its role as a ligand in coordination chemistry, where it can bind to metal ions to form coordination compounds. The compound's chemical formula is C27H21O, reflecting its composition of carbon, hydrogen, and oxygen atoms. Its synthesis typically involves multi-step organic reactions, and it is often used as a research tool to study the properties of aromatic compounds and their interactions with other molecules.

2892-40-2

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2892-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2892-40-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2892-40:
(6*2)+(5*8)+(4*9)+(3*2)+(2*4)+(1*0)=102
102 % 10 = 2
So 2892-40-2 is a valid CAS Registry Number.

2892-40-2Relevant academic research and scientific papers

Studies on the tandem reaction of 4-aryl-2,3-allenoates with organozinc reagents: A facile route to polysubstituted naphthols

Chai, Guobi,Lu, Zhan,Fu, Chunling,Shengming, Ma.

supporting information; experimental part, p. 11083 - 11086 (2010/04/26)

A highly efficient tandem reaction of easily available 4-aryl-2,3- allenoates with organozinc reagents was developed to afford the diversified polysubstituted anaphthols in moderate to excellent yields. A solution of 4-bromophenyl zinc iodide and xylenes

Metal-catalyzed cyclopropene rearrangements for benzannulation: Evaluation of an anthraquinone synthesis pathway and reevaluation of the parallel approach via carbene-chromium complexes

Semmelhack,Ho, Suzzy,Cohen,Steigerwald,Lee,Lee,Gilbert, Adam M.,Wutff, William D.,Ball, Richard G.

, p. 7108 - 7122 (2007/10/02)

The reaction of 3-arylcyclopropenes with Cr(CO)6 and Mo(CO)6 produces naphthols, in an example of metal-promoted benzannulation. Substituents at C- 3 (in addition to aryl) have a strong effect on the success of the process: 3-H deriv

Phototransformations of Epoxyindanone Adducts. Steady-State and Laser Flash Photolysis Studies

Ramaiah, Danaboyina,Rajadurai, Sivanandi,Das, Paritosh K.,George, Manapurathu V.

, p. 1082 - 1089 (2007/10/02)

The phototransformations of several cycloadducts of 2,3-diphenyl-2,3-epoxy-1-indanone are reported.All these substrates exhibited singlet-state-mediated transformations leading to benzoxocinones, whereas in some cases, depending on the substituents presen

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