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22975-57-1

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22975-57-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22975-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,7 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22975-57:
(7*2)+(6*2)+(5*9)+(4*7)+(3*5)+(2*5)+(1*7)=131
131 % 10 = 1
So 22975-57-1 is a valid CAS Registry Number.

22975-57-1Relevant academic research and scientific papers

Arene-catalysed lithiation of fluoroarenes

Guijarro, David,Yus, Miguel

, p. 1135 - 1138 (2000)

The reaction of different fluoroarenes 1 with lithium and a catalytic amount (7%) of naphthalene in THF at -30°C affords the corresponding aryllithium intermediates which, by reaction with several electrophiles at temperatures ranging between -30 and 0°C, lead to the expected products 2, after hydrolysis. (C) 2000 Elsevier Science Ltd.

INDOLE-DERIVATIVE MODULATORS OF STEROID HORMONE NUCLEAR RECEPTORS

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Page 105, (2010/02/07)

The present invention provides a compound of formula I or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising an effective amount of a compound of Formula I in combination with a suitable carrier, diluent, or excipient, and methods for treating physiological disorders, particularly congestive heart disease, comprising administering to a patient in thereof an effective amount of a compound of Formula I.

Transition-State Polarization in Cleavage of C-C Bonds in Radical Anions

Maslak, Przemyslaw,Narvaez, Javier N.,Kula, Jozef,Malinski, David S.

, p. 4550 - 4559 (2007/10/02)

The substituent effect on the rate of C-C bond cleavage in radical anions of 1-(4-nitrophenyl)-2-(substituted-phenyl)-1,1,2,2-tetraethylethanes has been explored.The data provide evidence for two distinctive modes of bond scission.One mode is characterized by a significant negative charge transfer across the scissile bond in the transition state.Such polarization of the transition state is in contradiction to the prediction based on the fragments' stability.The second mode, dominant in cases where the charge shift leads to negative charge accumulation on an already electron-rich fragment, involves a ?* radical anion.Both modes point to a general kinetic preference for a cleavage of radical anions that allows for charge delocalization across the scissile bond.

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