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Anthracene, 9-bromo-10-[4-(1,1-dimethylethyl)-2,6-dimethylphenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

648418-76-2

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648418-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 648418-76-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,4,1 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 648418-76:
(8*6)+(7*4)+(6*8)+(5*4)+(4*1)+(3*8)+(2*7)+(1*6)=192
192 % 10 = 2
So 648418-76-2 is a valid CAS Registry Number.

648418-76-2Downstream Products

648418-76-2Relevant academic research and scientific papers

A tris(carbene) constructed with stable triplet carbene units

Tsuchiya, Yoko,Matsuno, Masayoshi,Itoh, Tetsuji,Hirai, Katsuyuki,Tomioka, Hideo

, p. 2037 - 2050 (2007/10/03)

Bis[10-(4-t-butyl-2,6-dimethylphenyl)-9-anthryl]diazomethane, which can generate a fairly stable triplet carbene that can survive for even a week in solution at room temperature, was shown to be stable enough to undergo a Sonogashira coupling reaction. Th

Preparation of bis(diazo) compounds incorporated into butadiyne and thiophene units, and generation and characterization of Bis(carbene) from these compounds

Itoh, Tetsuji,Morisaki, Fumika,Hirai, Katsuyuki,Tomioka, Hideo

, p. 5870 - 5880 (2007/10/03)

[9-{10-(4-t-Butyl-2,6-dimethyl)phenyl}anthryl](4-bromo-2,6-dimethylphenyl) diazomethane(1-N2) was found to be stable enough to survive under Sonogashira and Suzuki coupling reaction conditions, and bis(diazo) compounds incorporated into the 1,4

Preparation of Oligodiazo Compounds by Using the Suzuki Coupling Reaction and Characterization of Their Photoproducts

Itoh, Tetsuji,Hirai, Katsuyuki,Tomioka, Hideo

, p. 1130 - 1140 (2007/10/03)

[9-{10-(4-tert-Butyl-2,6-dimethyl)phenyl}anthryl](4-bromo-2, 6-dimethylphenyl)diazomethane was found to be stable enough to survive under Suzuki coupling conditions and underwent mono-, di-, and trisubstitution with benzene mono-, di-, and triboronic acid

A Triplet Carbene Surviving a Week in Solution at Room Temperature

Iwamoto, Eri,Hirai, Katsuyuki,Tomioka, Hideo

, p. 14664 - 14665 (2007/10/03)

A stable triplet carbene, having a lifetime at 25 °C of 14.5 days in a dilute benzene solution, was realized by simply changing the substituent at the 10 position of the previously most persistent carbene, di[9-(10-phenyl)anthryl]carbene, from a phenyl to

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