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1,1'-Biphenyl, 2-(1,1-dimethylethyl)-, also known as 2-tert-butylbiphenyl, is an organic compound with the chemical formula C16H18. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. 1,1'-Biphenyl, 2-(1,1-dimethylethyl)- is a derivative of biphenyl, where a tert-butyl group (1,1-dimethylethyl) is attached to the 2-position of the biphenyl molecule. 2-tert-butylbiphenyl is used as a chemical intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. It is also employed as a ligand in coordination chemistry and as a building block in the construction of more complex organic molecules. Due to its aromatic nature, it exhibits certain electronic properties that make it useful in various applications, such as in materials science and as a component in specialty chemicals.

2113-53-3

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2113-53-3 Usage

Physical state

Colorless to light yellow liquid

Solubility

Soluble in organic solvents such as ethanol and acetone

Uses

a. Heat transfer fluid
b. Solvent in organic synthesis
c. Dispersant in the formulation of various products
d. Intermediate in the production of dyes, pharmaceuticals, and other organic compounds

Health hazards

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

Environmental impact

May have harmful effects on aquatic organisms

Safety precautions

Proper safety precautions and handling procedures should be followed when working with 1,1'-Biphenyl, 2-(1,1-dimethylethyl)-

Check Digit Verification of cas no

The CAS Registry Mumber 2113-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2113-53:
(6*2)+(5*1)+(4*1)+(3*3)+(2*5)+(1*3)=43
43 % 10 = 3
So 2113-53-3 is a valid CAS Registry Number.

2113-53-3Downstream Products

2113-53-3Relevant academic research and scientific papers

Palladium-catalyzed arylation of simple arenes with iodonium salts

Storr, Thomas E.,Greaney, Michael F.

supporting information, p. 1410 - 1413 (2013/05/09)

The development of an arylation protocol for simple arenes with diaryliodonium salts using the Herrmann-Beller palladacycle catalyst is reported. The reaction takes simple aromatic feedstocks and creates valuable biaryls for use in all sectors of the chem

Non-catalytic conversion of C-F bonds of benzotrifluorides to C-C bonds using organoaluminium reagents

Terao, Jun,Nakamura, Misaki,Kambe, Nobuaki

scheme or table, p. 6011 - 6013 (2010/11/16)

A facile method for the conversion of C-F bonds of benzotrifluorides to C-C bonds has been developed using aluminium reagents in the absence of catalysts.

MOFs as acid catalysts with shape selectivity properties

Ravon, Ugo,Domine, Marcelo E.,Gaudillere, Cyril,Desmartin-Chomel, Arnold,Farrusseng, David

, p. 937 - 940 (2008/12/20)

MOFs permit the paraalkylation of large polyaromatic compounds with nearly 100% of regioselectivity, offering new alternatives to standard zeolite catalysts. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.

Synthesis of 4-alkyl-4-(4-methoxyphenyl)cyclohex-2-en-1-ones and 5-alkyl-5-phenyl-1,3-cyclohexadienes from bis(tricarbonylchromium)-coordinated biphenyls

Rieke, Reuben D.,Schulte, Louis D.,Dawson, Bryan T.,Yang, Sheng Sbeng

, p. 8388 - 8398 (2007/10/02)

(η6:η6-Biphenyl)[Cr(CO)3] 2 and (η6η64,4'-dimethoxybiphenyl) [Cr(CO)3]2 were chemically reduced with lithium anthracenide or lithium naphthalenide in THF to generate s

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