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[1,1':3',1''-Terphenyl]-2'-carboxylic acid, 4,4''-dimethyl-, 1,2-ethanediyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

155186-08-6

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155186-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155186-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,1,8 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155186-08:
(8*1)+(7*5)+(6*5)+(5*1)+(4*8)+(3*6)+(2*0)+(1*8)=136
136 % 10 = 6
So 155186-08-6 is a valid CAS Registry Number.

155186-08-6Downstream Products

155186-08-6Relevant academic research and scientific papers

Meta-terphenyls as building blocks for benzimidazolophanes

Rajakumar, Perumal,Srisailas, Muthialu

, p. 5323 - 5326 (1997)

Coupling of the dibromide 4 and the tetrabromide 6 with benzimidazole gave the benzimidazolophanes 1 and 2 respectively.

Synthesis of cyclophanes with intra-annular functionality and cage structure

Kannan, Arunachalam,Rajakumar, Perumal,Kabaleeswaran,Rajan

, p. 5090 - 5102 (2007/10/03)

Cyclophanes of the type 1 and 2, with large cavity sizes, have been synthesized from the corresponding dichloride 8 or 8a and o-xylene-α,α′-dithiol (9), p-xylene-α,α′-dithiol (10), or m-terphenyldithiol (11). Similarly, cyclophanes of the type 3 with intr

2′-Substituted meta-terphenyls as building blocks for cyclophanes with intra-annular functionality

Hart, Harold,Rajakumar, Perumal

, p. 1313 - 1336 (2007/10/02)

2′-Substituted m-terphenyls containing chloromethyl and/or thiomethyl groups at the 4,4″ or 3,3″ positions are used as building blocks for cyclophanes with intra-annular functionality. Syntheses are short and yields are good. The methodology, capable of w

Synthesis of functionalised cyclophanes with cage structure; via an unusual termolecular collision

Rajakumar,Kannan

, p. 8317 - 8320 (2007/10/02)

Coupling of the tetrathiol 11 with two equivalents of the dibromide 6,7 and 8 under high dilution technique in the presence of KOH in benzene-ethanol afforded the cyclophanes 1a, 1c and 1b respectively. Similarly cyclophane 1d was obtained from the tetrat

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