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1,2-Ethanediamine, N,N'-bis(4-bromophenyl)-1,2-diphenyl- is a complex organic compound with the chemical formula C20H18Br2N2. It is a derivative of 1,2-ethanediamine, featuring two 4-bromophenyl groups attached to the nitrogen atoms and two phenyl groups attached to the carbon atoms. 1,2-Ethanediamine, N,N'-bis(4-bromophenyl)-1,2-diphenyl- is characterized by its symmetrical structure and the presence of bromine atoms, which contribute to its unique chemical properties. It is primarily used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its ability to form stable complexes with metal ions. The compound's molecular weight is 450.17 g/mol, and it is soluble in organic solvents. It is important to handle 1,2-Ethanediamine, N,N'-bis(4-bromophenyl)-1,2-diphenyl- with care, as it may have potential health risks and should be stored away from heat and open flames.

2849-15-2

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2849-15-2 Usage

General Description

1,2-Ethanediamine, N,N'-bis(4-bromophenyl)-1,2-diphenyl- is a chemical compound that belongs to the class of diamines. It is also known as 4,4'-Diamino-1,1'-biphenyl-3,3'-dibromide and is used as a building block in the synthesis of various organic compounds. It is commonly used as a reagent in organic synthesis and as a precursor in the production of polymers, pharmaceuticals, and agrochemicals. This chemical has two amine groups and two phenyl groups, making it useful in forming complex organic structures. It is important to handle 1,2-Ethanediamine, N,N'-bis(4-bromophenyl)-1,2-diphenyl- with caution as it can be hazardous if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 2849-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,4 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2849-15:
(6*2)+(5*8)+(4*4)+(3*9)+(2*1)+(1*5)=102
102 % 10 = 2
So 2849-15-2 is a valid CAS Registry Number.

2849-15-2Downstream Products

2849-15-2Relevant academic research and scientific papers

Highly chemoselective crossed imino pinacol coupling reaction using the synergetic effect of boron trifluoride etherate and trichloromethylsilane

Shimizu, Makoto,Suzuki, Ikuhiro,Makino, Hiroaki

, p. 1635 - 1638 (2007/10/03)

Use of boron trifluoride etherate and trichloromethylsilane in the presence of zinc-copper couple effects a crossed imino pinacol coupling reaction to give 1,2-diamines in good yields with high diastereoselectivities.

Reductive coupling of aldimines mediated with samarium catalyzed by Cp2TiCl2

Liao, Puhong,Huang, You,Zhang, Yongmin

, p. 1483 - 1486 (2007/10/03)

Reductive coupling of aldimines into vicinal diamines mediated with samarium catalyzed by Cp2TiCl2 proceeds in refluxing THF with good yields.

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