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1059628-81-7

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1059628-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1059628-81-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,9,6,2 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1059628-81:
(9*1)+(8*0)+(7*5)+(6*9)+(5*6)+(4*2)+(3*8)+(2*8)+(1*1)=177
177 % 10 = 7
So 1059628-81-7 is a valid CAS Registry Number.

1059628-81-7Relevant articles and documents

COMPOUNDS FOR MODULATING DDAH AND ADMA LEVELS, AS WELL AS METHODS OF USING THEREOF TO TREAT DISEASE

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Page/Page column 97; 98, (2019/11/19)

Disclosed are compounds that can modulate DDAH and the amount of asymmetric dimethylarginine (ADMA) in a subject. Also provided are pharmaceutical compositions comprising these compounds, as well as methods of using these compositions to treat and/or prevent diseases associated with elevated or low levels of DDAH and ADMA.

Copper catalysed domino decarboxylative cross coupling-cyclisation reactions: Synthesis of 2-arylindoles

Ponpandian, Thanasekaran,Muthusubramanian, Shanmugam

, p. 4248 - 4252 (2012/08/28)

The efficient synthesis of 2-arylindoles and 6H-isoindolo[2,1-a]indol-6-one through copper catalysed domino sp-sp2 decarboxylative cross-coupling and subsequent cyclisation reactions of arylpropiolic acids with 2-iodotrifluoroacetanilide has been described. This methodology also demonstrates that indolo[1,2-c]quinazolin-6(5H)-one can be obtained with the elimination of trifluoromethyl anion.

Structure-activity relationships of 2-aryl-1H-indole inhibitors of the NorA efflux pump in Staphylococcus aureus

Ambrus, Joseph I.,Kelso, Michael J.,Bremner, John B.,Ball, Anthony R.,Casadei, Gabriele,Lewis, Kim

scheme or table, p. 4294 - 4297 (2009/04/06)

The synthesis of 22 2-aryl-1H-indoles, including 12 new compounds, has been achieved via Pd- or Rh-mediated methodologies, or selective electrophilic substitution. All three methods were based on elaborations from simple indole precursors. SAR studies on

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