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2-([1,1'-BIPHENYL]-2-YLOXY)ANILINE, also known as 2-(2-phenoxyphenyl)aniline or 2-(2-biphenyl-2-yloxy)aniline, is an organic compound with the chemical formula C18H15NO. It is a derivative of aniline, where one of the hydrogen atoms on the aniline nitrogen is replaced by a 2-phenoxyphenyl group. 2-([1,1'-BIPHENYL]-2-YLOXY)ANILINE is characterized by its aromatic structure, which includes a biphenyl moiety and an aniline group. It is used in various applications, such as in the synthesis of dyes, pharmaceuticals, and other organic compounds. Due to its chemical structure, it may exhibit properties such as reactivity with electrophiles and nucleophiles, and it is typically handled with care due to its potential reactivity and the need to manage its environmental impact.

2688-92-8

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2688-92-8 Usage

Physical state

Pale yellow to brown solid

Usage

Production of dyes, pharmaceuticals, and other organic compounds

Common application

Intermediate in the synthesis of various chemicals

Known for

Aromatic properties

Toxicity

Toxic

Health hazards

Can cause irritation to the skin, eyes, and respiratory tract

Safety measures

Proper handling and protective measures are necessary when working with O-anisidine.

Check Digit Verification of cas no

The CAS Registry Mumber 2688-92-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2688-92:
(6*2)+(5*6)+(4*8)+(3*8)+(2*9)+(1*2)=118
118 % 10 = 8
So 2688-92-8 is a valid CAS Registry Number.

2688-92-8Relevant academic research and scientific papers

Synthesis of Cycloheptatrienes, Oxepines, Thiepines, and Silepines: A Comparison between Br?nsted Acid and Au-Catalysis

Alcarazo, Manuel,Golz, Christopher,Sprenger, Kristin

supporting information, p. 6245 - 6254 (2020/10/02)

The cyclization of 1-(benzyl-, oxyaryl-, thioaryl-, and silaaryl)-2-ethynylbenzenes under Br?nsted acid- and Au(I)-catalysis is described. Br?nsted acid catalysis favors without exception the formation of the products derived from the regioselective proto

Synthesis and enantioselective hydrogenation of seven-membered cyclic imines: Substituted dibenzo[b,f][1,4]oxazepines

Gao, Kai,Yu, Chang-Bin,Li, Wei,Zhou, Yong-Gui,Zhang, Xumu

supporting information; experimental part, p. 7845 - 7847 (2011/09/13)

Highly enantioselective hydrogenation of seven-membered cyclic imines, substituted dibenzo[b,f][1,4]oxazepines, was achieved, with up to 94% ee, by using the [Ir(COD)Cl]2/(S)-Xyl-C3*-TunePhos complex as the catalyst in the presence of morpholine-HCl.

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