32740-31-1 Usage
Uses
Used in Research and Development:
D(7)-1,2,3-Hexan is used as a research compound for the study of chemical reactions and processes. Its isotopic labeling enables researchers to trace and analyze specific pathways and mechanisms within complex systems, providing valuable insights into the behavior of molecules and their interactions.
Used in Analytical Chemistry:
In Analytical Chemistry, D(7)-1,2,3-Hexan is used as a labeled internal standard for the quantification and identification of target compounds. Its unique isotopic signature allows for accurate measurement and comparison, enhancing the precision and reliability of analytical results.
Used in Pharmaceutical Industry:
Within the Pharmaceutical Industry, D(7)-1,2,3-Hexan is employed as a tool for drug development and optimization. Its isotopic properties can be leveraged to study the metabolism, distribution, and excretion of drug candidates, aiding in the design of more effective and safer medications.
Used in Environmental Science:
In Environmental Science, D(7)-1,2,3-Hexan is used as a tracer compound to investigate the fate and transport of pollutants in the environment. Its isotopic labeling allows for the tracking of specific contaminants and the assessment of their impact on ecosystems and human health.
Used in Material Science:
In Material Science, D(7)-1,2,3-Hexan is utilized as a component in the synthesis of advanced materials and the study of their properties. Its unique isotopic composition can provide insights into the structure and behavior of these materials, contributing to the development of innovative technologies and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 32740-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,4 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32740-31:
(7*3)+(6*2)+(5*7)+(4*4)+(3*0)+(2*3)+(1*1)=91
91 % 10 = 1
So 32740-31-1 is a valid CAS Registry Number.
32740-31-1Relevant academic research and scientific papers
Coles, Nathan T.,Linford-Wood, Thomas G.,Webster, Ruth L.
, p. 2703 - 2709 (2021)
Reduction of carbon-carbon double bonds is reported using a three-coordinate iron(ii) β-diketiminate pre-catalyst. The reaction is believed to proceedviaa formal transfer hydrogenation using poly(methylhydrosiloxane), PMHS, as the hydride donor and a bio-alcohol as the proton source. The reaction proceeds well usingn-butanol and ethanol, withn-butanol being used for substrate scoping studies. Allyl arene substrates, styrenes and aliphatic substrates all undergo reduction at room temperature. Unfortunately, clean transfer of a deuterium atom usingd-alcohol does not take place, indicating a complex catalytic mechanism. However, changing the deuterium source tod-aniline gives close to complete regioselectivity for mono-deuteration of the terminal position of the double bond. Finally, we demonstrate that efficient dehydrocoupling of alcohol and PMHS can be undertaken using the same pre-catalyst, giving high yields of H2within 30 minutes at room temperature.
