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78904-10-6

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78904-10-6 Usage

Family

Benzene family

Structure

Three bromine atoms and one chlorine atom attached to the benzene ring

Physical state at room temperature

White solid

Solubility

Insoluble in water

Applications

Building block in the synthesis of pharmaceuticals, agrochemicals, and dyes

Potential uses

Flame retardant in plastics, intermediate in the production of other brominated compounds

Safety precautions

Handle with caution, may be harmful if ingested, inhaled, or in contact with skin

Check Digit Verification of cas no

The CAS Registry Mumber 78904-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,0 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78904-10:
(7*7)+(6*8)+(5*9)+(4*0)+(3*4)+(2*1)+(1*0)=156
156 % 10 = 6
So 78904-10-6 is a valid CAS Registry Number.

78904-10-6Downstream Products

78904-10-6Relevant articles and documents

Polyfluorinated functionalized m-terphenyls. New substituents and ligands in organometallic synthesis

Olaru, Marian,Beckmann, Jens,Rat, Ciprian I.

supporting information, p. 3012 - 3020 (2014/07/08)

The synthesis and structural characterization of polyfluorinated arenes 2,4,6-(C6F5)3C6H2X and 2,6-(C6F5)2-4-BrC6H2X (X = NO2, Cl, Br) obtained in the Ullmann-type cross coupling reaction is reported. The nitro derivatives were reduced to the aromatic amines. The α-diimine [2,4,6-(C6F5)3C 6H2NCMe]2 and 2,4,6-(C6F 5)3C6H2I were obtained in condensation and Sandmeyer reactions, respectively, from the corresponding amine. The syntheses of 2,4,6-(C6F5)3C 6H2NHC(O)H, 2,4,6-(C6F5) 3C6H2NC, and 2,4,6-(C6F 5)3C6H2Si(X)Me2 (X = H, F, Cl) are also described.

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