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1,3-Benzenedicarboxylic acid, 5,5'-[1,2-phenylenebis(methyleneoxy)]bis-, tetraethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

155186-12-2

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155186-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155186-12-2 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, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 155186-12:
(8*1)+(7*5)+(6*5)+(5*1)+(4*8)+(3*6)+(2*1)+(1*2)=132
132 % 10 = 2
So 155186-12-2 is a valid CAS Registry Number.

155186-12-2Relevant academic research and scientific papers

Synthesis of cyclophanes with intra-annular functionality and cage structure

Kannan, Arunachalam,Rajakumar, Perumal,Kabaleeswaran,Rajan

, p. 5090 - 5102 (1996)

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

Synthesis and structural analysis of isomeric pyridinophanes and thiacyclophanes

Rajakumar, Perumal,Dhanasekaran, Manickam,Selvanayagam, Sivashanmugam,Rajakannan, Venkatachalam,Velmurugan, Devadasan,Ravikumar, Krishnan

, p. 995 - 999 (2007/10/03)

A one-pot synthesis of structurally isomeric tetrathiacyclophanes through four-centre coupling reactions of suitable bromides and thiols is reported. The structures of the isomers were confirmed by spectroscopy and XRD analysis. Single crystal X-ray analy

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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