284474-41-5 Usage
Description
1-BROMOHEXADECANE-D33 is a deuterated compound, which is an isotopically labeled research compound. It is primarily used in the field of chemistry and biochemistry for various applications, including the preparation of lipophilic nucleosides.
Uses
Used in Chemical Synthesis:
1-BROMOHEXADECANE-D33 is used as a synthetic building block for the preparation of lipophilic nucleosides via esterification, amidation, and alkylation from uridine derivatives. This application is crucial in the development of new pharmaceutical compounds and the study of molecular interactions.
Used in Biochemical Research:
In the field of biochemistry, 1-BROMOHEXADECANE-D33 serves as an essential research compound. Its deuterated nature allows for the investigation of various biochemical processes and interactions, providing valuable insights into the mechanisms of biological systems.
Used in Pharmaceutical Development:
1-BROMOHEXADECANE-D33 is used as a key component in the development of new pharmaceuticals. Its role in the synthesis of lipophilic nucleosides contributes to the creation of novel drug candidates with potential therapeutic applications.
Used in Analytical Chemistry:
In analytical chemistry, 1-BROMOHEXADECANE-D33 can be employed as a reference compound or internal standard for the accurate quantification and identification of similar compounds in complex mixtures. Its deuterated nature makes it an ideal choice for such applications.
Used in Material Science:
1-BROMOHEXADECANE-D33 may also find applications in material science, particularly in the development of new materials with specific properties. Its unique chemical structure and deuterated nature can be exploited to create materials with tailored characteristics for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 284474-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,4,4,7 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 284474-41:
(8*2)+(7*8)+(6*4)+(5*4)+(4*7)+(3*4)+(2*4)+(1*1)=165
165 % 10 = 5
So 284474-41-5 is a valid CAS Registry Number.
284474-41-5Relevant articles and documents
Inter- and intramolecular temperature-dependent vibrational perturbations of alkanethiol self-assembled monolayers
Garand, Eì?tienne,Picard, Jean-Francì§ois,Rowntree, Paul
, p. 8182 - 8189 (2007/10/03)
The infrared spectra of octanethiol, dodecanethiol, and hexadecanethiol (C8, C12, and C16, respectively) monolayers adsorbed on Au(111) textured surfaces have been explored in the 25-300 K regime. The C-H stretching modes typically shift by several wavenumbers to lower frequencies and the intensities increase by as much as 75% as the temperature is decreased, providing evidence of, among other effects, the coupling of these stretching modes with lower energy vibrational modes. In contrast, for all temperatures below 300 K, the positions of the C-H bands of fully hydrogenated C16, shift by several wavenumbers to higher frequencies as the hydrogenated adsorbates are increasingly diluted in a matrix of fully deuterated C16, showing that all bands are subject to intermolecular couplings. The analysis of the behavior of the C-H stretching bands suggests that the temperature dependence of the vibrational frequencies associated with the methylene stretching modes is principally due to intermolecular couplings, whereas the temperature dependence of the vibrations associated with the methyl terminations is largely due to intramolecular couplings. It is suggested that the highly constrained geometry of the isotopically diluted monolayer may provide an environment that is less sensitive to intramolecular couplings with low-frequency modes than that of urea-clathrate-isolated species.
