14629-70-0 Usage
Uses
Used in Research and Development:
2-Pentyl-1,1,1,3,3-D5 Alcohol is used as a research compound for the study of chemical reactions and processes. Its isotopic labeling enables scientists to track and analyze specific pathways and mechanisms, contributing to a better understanding of the underlying chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Pentyl-1,1,1,3,3-D5 Alcohol is used as a labeled compound for the development and testing of new drugs. Its unique properties allow researchers to study the interactions between the compound and biological systems, aiding in the design and optimization of potential therapeutic agents.
Used in Chemical Synthesis:
2-Pentyl-1,1,1,3,3-D5 Alcohol is also used as a labeled building block in the synthesis of various chemical compounds. Its isotopic labeling can help researchers identify and isolate specific products, facilitating the development of new materials and chemicals with desired properties.
Used in Analytical Chemistry:
In the field of analytical chemistry, 2-Pentyl-1,1,1,3,3-D5 Alcohol is employed as a labeled reference material for the calibration and validation of analytical instruments and methods. Its unique isotopic signature allows for accurate measurements and quantification of target compounds, ensuring the reliability and accuracy of analytical results.
Used in Environmental Studies:
2-Pentyl-1,1,1,3,3-D5 Alcohol can be utilized in environmental research as a labeled tracer to study the fate and transport of pollutants in the environment. Its isotopic labeling enables the tracking of specific contaminants, providing valuable insights into their behavior and potential impacts on ecosystems and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 14629-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,2 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14629-70:
(7*1)+(6*4)+(5*6)+(4*2)+(3*9)+(2*7)+(1*0)=110
110 % 10 = 0
So 14629-70-0 is a valid CAS Registry Number.
14629-70-0Relevant academic research and scientific papers
CH-π interaction as an important driving force of host-guest complexation in apolar organic media. Binding of monools and acetylated compounds to resorcinol cyclic tetramer as studied by 1H NMR and circular dichroism spectroscopy
Kobayashi, Kenji,Asakawa, Yuji,Kikuchi, Yasuaki,Toi, Hiroo,Aoyama, Yasuhiro
, p. 2648 - 2653 (2007/10/02)
The CH-π interaction plays an important role in the complexation involving resorcinol cyclic tetramer 1 in chloroform. Thus, host 1 binds simple monools 4-10 via a cooperation of CH-π and hydrogen-bonding interactions, where the binding constants at 298 K (up to 13 M-1) increase with increasing chain lengths (from ethyl through propyl to butyl) as well as branching in the aliphatic moiety of the guests. In addition, the largest complexation-induced 1H NMR upfield shift for a bound guest occurs at the terminal methyl group, which must therefore be deeply incorporated in the aromatic cavity of the host. The complexes derived from chiral secondary alcohols 10-17 including terpenes and steroids exhibit induced circular dichroism as a result of guest-to-host chirality transfer which is mediated by the CH-π interaction. Borneol (14) having three methyl groups to allow a multipoint CH-π interaction forms a particularly stable complex (K = 54 M-1). The acetyl group in a guest is significantly complexation-promoting. This is primarily due to enhanced CH-π interaction involving the polarized C-H bonds of the acetyl group. The binding constants for selected guests are K = 35, 12, 4, and 1 M-1 for 3-oxo-1-butanol (simple alcohol having an acetyl group), bornyl acetate (monoacetate having a bulky and highly branched aliphatic moiety), 2,4-diacetoxypentane (simple diacetate), and cholestane (bulky hydrocarbon), respectively.
