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170159-24-7

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170159-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170159-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,1,5 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 170159-24:
(8*1)+(7*7)+(6*0)+(5*1)+(4*5)+(3*9)+(2*2)+(1*4)=117
117 % 10 = 7
So 170159-24-7 is a valid CAS Registry Number.

170159-24-7Relevant articles and documents

Molecular electronics - Integration of single molecules in electronic circuits

Mayor, Marcel,Weber, Heiko B.

, p. 494 - 499 (2002)

Electronic devices made with organic molecules may one day play an important role in integrated circuits. However, the research is still in its infancy. The mechanically controlled break-junction technique allows the measurement of the current through a s

Bismuth(III)-Promoted Acetylation of Thioethers into Thioacetates

Jevric, Martyn,Petersen, Anne Ugleholdt,Mans?, Mads,Madsen, Anders,Nielsen, Mogens Br?ndsted

, p. 4675 - 4688 (2015/08/03)

The thioacetate group is extensively employed as an anchoring group for attachment of molecules onto gold surfaces or between electrodes in molecular electronics. On account of its ready hydrolysis, it is often incorporated in the last step of a synthetic

Conformation as a protecting group: A regioselective aromatic bromination en route to complex π-electron systems

Guthrie, Daryl A.,Tovar, John D.

supporting information; body text, p. 4323 - 4326 (2009/06/06)

(Chemical Equation Presented) A new strategy to achieve regioselective functionalization of a sterically congested aromatic system driven by conformational demands is described. Electrophilic substitution occurs at the more planarizable subunit without undesired chemistry at mutually reactive sites and without the need for protecting or masking groups that must be manipulated later. Model studies are described to understand this selectivity, and possibilities for the construction of orthogonal, differentially substituted π-systems of relevance for molecular electronics are demonstrated.

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