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9,10-bis-(4-bromophenyl)-3,6-dibromophenanthrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1257666-22-0

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1257666-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1257666-22-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,7,6,6 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1257666-22:
(9*1)+(8*2)+(7*5)+(6*7)+(5*6)+(4*6)+(3*6)+(2*2)+(1*2)=180
180 % 10 = 0
So 1257666-22-0 is a valid CAS Registry Number.

1257666-22-0Downstream Products

1257666-22-0Relevant academic research and scientific papers

Synthesis and property of new propeller shaped emitting materials for organic light-emitting devices

Kang, Seokwoo,Lee, Hayoon,Kim, Beomjin,Park, Youngil,Park, Jongwook

, p. 3102 - 3105 (2016)

New propeller type emitting compound, namely 3,6-di-anthracen-9-yl-9,10-bis-(4-anthracen- 9-yl-phenyl)-phenanthrene[TAnDAP] and 3,6-bis-(10-phenyl-anthracen-9-yl)-9,10-bis-[4-(10-phenylanthracen- 9-yl)-phenyl]-phenanthrene [TAnPDAP] were synthesized through Suzuki and McMurry reactions. We investigated their physical properties such as optical, electrochemical, and electroluminescent properties. The two compounds were used as an emitting layer in OLED devices: ITO/2-TNATA (60 nm)/NPB (15 nm)/non-doped: TAnDAP or TAnPDAP (35 nm)/Alq3 (20 nm)/LiF (1 nm)/Al (200 nm). The TAnDAP OLED device showed C.I.E. value of (0.28, 0.41) and luminance efficiency of 3.81 cd/A at 10 mA/cm2. The TAnPDAP device showed C.I.E. value of (0.20, 0.27) and high luminance efficiency of 5.40 cd/A at 10 mA/cm2. TAnPDAP was found to show better luminance efficiency and C.I.E. value than TAnDAP because it has a bulky 9-phenylanthracene.

Sequential oxidative transformation of tetraarylethylenes to 9,10-diarylphenanthrenes and dibenzo[g, p]chrysenes using DDQ as an oxidant

Navale, Tushar S.,Thakur, Khushabu,Rathore, Rajendra

supporting information; experimental part, p. 1634 - 1637 (2011/05/06)

Tetraarylethylenes can be sequentially transformed into 9,10-diarylphenanthrenes and dibenzo[g,p]chrysenes using 1 and 2 equiv of DDQ, respectively, in CH2Cl2 containing methanesulfonic acid, in excellent yields. Efficient access to substituted dibenzochrysenes from tetraarylethylenes establishes the versatility of this procedure over the existing multistep syntheses of dibenzochrysenes. Moreover, the ready regeneration of DDQ from easily recovered reduced DDQ-H2 continues to advance the use of DDQ/H+ for the oxidative C-C bond forming reactions.

Synthesis and redox behavior of novel 9,10-diphenylphenanthrenes

Schreivogel, Alina,Sieger, Monika,Baro, Angelika,Laschat, Sabine

experimental part, p. 1912 - 1924 (2010/12/25)

The synthesis and electrochemical investigations of 9,10- diphenylphenanthrene 2a and its derivatives 2b-2e are reported. The cyclic voltammetry of derivatives 2a-2c and 2e in different solvent/Bu 4NPF6 electrolyte systems reveals th

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