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93253-73-7

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93253-73-7 Usage

Uses

Reactant for:Metal-catalyzed allylic substitution reactionSynthesis of an anti-methicillin-resistant staphylococcus aureus (MRSA) carbapenem via stannatrane mediated Stille coupling

Check Digit Verification of cas no

The CAS Registry Mumber 93253-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,5 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93253-73:
(7*9)+(6*3)+(5*2)+(4*5)+(3*3)+(2*7)+(1*3)=137
137 % 10 = 7
So 93253-73-7 is a valid CAS Registry Number.

93253-73-7 Well-known Company Product Price

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  • Aldrich

  • (707562)  5-Chloro-1-aza-5-stanna-bicyclo[3.3.3]undecane  

  • 93253-73-7

  • 707562-500MG

  • 1,539.72CNY

  • Detail
  • Aldrich

  • (707562)  5-Chloro-1-aza-5-stanna-bicyclo[3.3.3]undecane  

  • 93253-73-7

  • 707562-2G

  • 5,335.20CNY

  • Detail

93253-73-7Relevant articles and documents

PENTACOORDINATED TETRAORGANOTIN AND SILICON COMPOUNDS-SYNTHESIS AND STRUCTURES.

Tzschach,Jurkschat

, p. 639 - 646 (1985)

Starting from di- and trifunctional Grignard reagents of the general types E(CH//2CH//2CH//2MgCl)//2 (E equals NMe, O, S) and N(CH//2CH//2MgCl)//3 the cyclic organotin and organosilicon compounds R//2M(CH//2CH//2CH//2)//2E and RM(CH//2CH//2CH//2)//3N (M equals Si, Sn; R equals Cl, Br, I, CH//3) are described. X-ray studies confirm these compounds to exhibit pentacoordinated structures with intramolecular donor-acceptor interactions. The strength of these interactions depends from the nature of the substituents bonded to the metal center. The dynamic processes which are observed by nmr investigations are interpreted in terms of a dissociation-inversion mechanism and an 'in-out' equilibrium. First results are reported concerning the preparation of a two nitrogen containing difunctional Grignard reagent and its reaction with tin tetrachloride providing hexacoordinated tin compounds.

Internal Coordination at Tin Promotes Selective Alkyl Transfer in the Stille Coupling Reaction

Vedejs, Edwin,Haight, Anthony R.,Moss, William O.

, p. 6556 - 6558 (2007/10/02)

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