56804-58-1 Usage
Uses
Used in Pharmaceutical Industry:
Trimethylsilyl cyanide-13C is used as a reagent in the synthesis of optically active cyanohydrins. These cyanohydrins are essential intermediates in the production of various pharmaceutical compounds, as they can be further converted into valuable chiral building blocks and enantiomerically pure drugs.
Used in Organic Chemistry Research:
In the field of organic chemistry, Trimethylsilyl cyanide-13C is employed in the preparation of Reissert compounds. Reissert compounds are reactive polyamides that serve as versatile intermediates in the synthesis of a wide range of organic molecules, including natural products, pharmaceuticals, and agrochemicals. The use of 13C-labeled trimethylsilyl cyanide allows researchers to study the reaction mechanisms and pathways involving these compounds.
Used in Toxicology Studies:
Trimethylsilyl cyanide-13C is also used in toxicology studies to investigate the toxic effects of the compound on humans. The isotope labeling allows for the tracking of the compound's distribution, metabolism, and excretion in the body, providing valuable insights into its toxicokinetics and potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 56804-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,0 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56804-58:
(7*5)+(6*6)+(5*8)+(4*0)+(3*4)+(2*5)+(1*8)=141
141 % 10 = 1
So 56804-58-1 is a valid CAS Registry Number.
56804-58-1Relevant academic research and scientific papers
Stern, Alfred G.,Ilao, Martin C.,Nickon, Alex
, p. 8107 - 8118 (1993)
Homobrexan-2-one was synthesized labeled in the α-position with 13C and also with an axial or equatorial D.Their p-tosylhydrazone Li salts were thermolyzed and photolyzed (Bamford-Stevens reaction) to generate putative singlet carbenes, which undergo competitive 1,3-insertion to a tetracycle and 1,2-H (or D) shift to an alkene.After correction for isotope effects, the Hax/Heq shift ratios were ca. 1.7 and ca. 1.2 for the thermal and photic processes, respectively.These ratios are free of chair-boat and epimerization ambiguities.
