89186-79-8 Usage
Uses
Used in Pharmaceutical Production:
ACETYL CHLORIDE-13C2 is used as a reagent in the synthesis of various pharmaceutical compounds due to its high reactivity, enabling the formation of acetyl derivatives and esters that are essential in drug development.
Used in Agricultural Chemicals:
In the agricultural sector, ACETYL CHLORIDE-13C2 serves as a key component in the production of certain agricultural chemicals, leveraging its reactivity to create compounds that can be used in crop protection and enhancement.
Used in Organic Synthesis:
ACETYL CHLORIDE-13C2 is utilized as a versatile building block in organic synthesis, where its ability to form acetyl derivatives and esters is crucial for creating a range of organic compounds.
Used in Nuclear Magnetic Resonance (NMR) Spectroscopy:
ACETYL CHLORIDE-13C2 is employed as an isotopic label in NMR spectroscopy, allowing for the tracking and identification of specific atoms within complex molecular structures, which is vital for understanding molecular dynamics and interactions.
Used in Isotope Labeling Studies:
In research, ACETYL CHLORIDE-13C2 is used as an isotope label to trace the metabolic pathways and biochemical transformations of compounds in biological systems, providing insights into metabolic processes and mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 89186-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,8 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89186-79:
(7*8)+(6*9)+(5*1)+(4*8)+(3*6)+(2*7)+(1*9)=188
188 % 10 = 8
So 89186-79-8 is a valid CAS Registry Number.
89186-79-8Relevant academic research and scientific papers
Synthesis of Proposed Chain-Elongation Intermediates of the Monensin Biosynthetic Pathway
Block, Michael H.,Cane, David E.
, p. 4923 - 4928 (2007/10/02)
Three proposed intermediates of the monensin biosynthetic pathway have been synthesized in 13C-labeled form.Treatment of propionyl N-acetylcysteamine (NAC) thioester 10 with 2 equiv of LDA followed by acylation with acetyl chloride gave
