39058-44-1 Usage
Description
BUTYROPHENONE-2',3',4',5',6'-D5 is an isotopically labeled research compound, which is a variant of the butyrophenone family with deuterium atoms incorporated into its structure. BUTYROPHENONE-2',3',4',5',6'-D5 is primarily used in scientific research and development, particularly in the field of chemistry and pharmaceuticals, to study the behavior and properties of the molecule.
Uses
Used in Research and Development:
BUTYROPHENONE-2',3',4',5',6'-D5 is used as a research compound for studying the properties and behavior of butyrophenone derivatives. The incorporation of deuterium atoms allows researchers to investigate the effects of isotopic substitution on the compound's reactivity, stability, and interaction with other molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, BUTYROPHENONE-2',3',4',5',6'-D5 can be used as a labeled reference material for the development and validation of analytical methods, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. This helps in the identification, quantification, and quality control of butyrophenone-based drugs and their metabolites.
Used in Chemical Synthesis:
BUTYROPHENONE-2',3',4',5',6'-D5 can also be employed as a starting material or intermediate in the synthesis of other deuterated compounds, which may have specific applications in various fields, such as drug development, materials science, and environmental chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 39058-44-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,5 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39058-44:
(7*3)+(6*9)+(5*0)+(4*5)+(3*8)+(2*4)+(1*4)=131
131 % 10 = 1
So 39058-44-1 is a valid CAS Registry Number.
39058-44-1Relevant articles and documents
Is the collosion induced loss of ethene from the (M - H+)- ion of butyrophenone a γ-hydrogen rearrangement?
Stringer, Michael B.,Underwood, Dennis J.,Bowie, John H.,Holmes, John L.,Mommers, Alexander A.,Szulejko, Jan E.
, p. 764 - 768 (2007/10/02)
The (M - H+)- ion of butyrophenone undergoes the following reactions on collisional activation: losses of CH3., CH4, (C,H5.), C2H4, C3H7., (CO + CH4), together with formation of C6H5- and C
