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357609-65-5

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357609-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 357609-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,6,0 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 357609-65:
(8*3)+(7*5)+(6*7)+(5*6)+(4*0)+(3*9)+(2*6)+(1*5)=175
175 % 10 = 5
So 357609-65-5 is a valid CAS Registry Number.

357609-65-5Relevant articles and documents

New macromolecular structures based on benzene core, synthesis and characterization

Ali, Mohammed Hadi,Torun, Lokman

, p. 465 - 472 (2021/09/28)

A series of new compounds based on benzene ring as a central core substituted with aromatic compounds such as (benzene and pyridine) and three armed of 2-chloro-4,6-bis((3,7-dimethyloct-6-en-1-yl) oxy)-1,3,5-triazine, have been obtained by sequential nucleophilic substitution of chlorine atoms in cyanuric chloride. The substitution at the acetylenic periphery on the central benzene ring has been achieved efficiently by Sonogashira coupling. Equimolar mixtures of the six-armed compounds based on the benzene core with the complementary 4-dodecyloxybenzoic acid, which already possessed liquid crystal property, has resulted in an organic salt. The obtained organic salts have been investigated by polarizing optical microscopy (POM) and differential scanning calorimetry (DSC). The synthesized compounds have been confirmed by spectroscopic methods (1H and13C NMR and mass spectromery).

One-pot synthesis of benzo[b]thiophenes and benzo[b]selenophenes from o-halo-substituted ethynylbenzenes: convenient approach to mono-, bis-, and tris-chalcogenophene-annulated benzenes

Kashiki, Tomoya,Shinamura, Shoji,Kohara, Masahiro,Miyazaki, Eigo,Takimiya, Kazuo,Ikeda, Masaaki,Kuwabara, Hirokazu

supporting information; experimental part, p. 2473 - 2475 (2009/10/18)

A convenient one-pot procedure for the synthesis of benzo[b]thiophenes and selenophenes from readily available o-halo-ethynylbenzene precursors is described. Regardless of the substituent on the acetylene terminus or the number of cyclization moieties on the precursors, various benzo[b]thiophenes and selenophenes, including not only the parent, alkyl-, and phenyl-substituted derivatives but also benzo[1,2-b:4,5-b']dithiophenes and diselenophenes and benzo[1,2-b:3,4-b':5,6-b'']trithiophenes and triselenophenes can be prepared in good to high yields.

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