Taiy Chemical
1,3-Dibromobenzene-d4
Product Name 1,3-Dibromobenzene-d4
Synonyms
CAS
EINECS
Molecular Weight 153.99 g/mol
Molecular Formula C6D4Br2
Density
Boiling Point(℃) 218.6
Flash Point(℃)
Refractive Index
Hazard Symbols
Risk Codes
Safety Description
FAQ
What is the significance of +1,3-Dibromobenzene-d4 in research applications?
+1,3-Dibromobenzene-d4 is a deuterated compound that is commonly used in research applications, particularly in the field of organic chemistry. This compound is valuable for its ability to serve as a precursor in the synthesis of various other compounds. Additionally, its deuterated form provides unique advantages for certain types of spectroscopic analyses, making it a crucial tool for researchers in the chemical sciences.

How does +1,3-Dibromobenzene-d4 differ from non-deuterated 1,3-Dibromobenzene?
The main difference between +1,3-Dibromobenzene-d4 and non-deuterated 1,3-Dibromobenzene lies in the presence of deuterium atoms in the former. Deuterium is a stable isotope of hydrogen that is commonly used in isotopic labeling studies. The incorporation of deuterium in the molecule alters its physical and chemical properties, making +1,3-Dibromobenzene-d4 a valuable tool for certain research applications where deuterium labeling is necessary.

What are some common uses of +1,3-Dibromobenzene-d4 in organic synthesis?
+1,3-Dibromobenzene-d4 is frequently used in organic synthesis as a starting material for the preparation of various compounds. It can undergo a range of chemical reactions, such as nucleophilic substitution and Heck coupling, to yield diverse products. Researchers utilize its unique reactivity and deuterium content to label specific positions in molecules or to introduce isotopic tags for tracing reaction pathways in complex organic syntheses.

How does the deuterated form of +1,3-Dibromobenzene impact spectroscopic analysis?
The deuterated form of +1,3-Dibromobenzene-d4 is particularly advantageous for certain types of spectroscopic analysis, such as NMR (nuclear magnetic resonance) spectroscopy. Deuterium has a different magnetic resonance frequency compared to hydrogen, allowing researchers to obtain clearer and more informative spectroscopic data. This makes +1,3-Dibromobenzene-d4 a valuable tool for studying molecular structures, dynamics, and interactions using spectroscopic techniques.

What are the benefits of using +1,3-Dibromobenzene-d4 in chemical research?
In chemical research, +1,3-Dibromobenzene-d4 offers several key benefits. Its deuterated form provides a unique means of isotopic labeling, enabling researchers to track the fate of specific atoms in a molecule during chemical reactions. This labeling strategy can offer valuable insights into reaction mechanisms, intermediate species, and product distributions. Additionally, +1,3-Dibromobenzene-d4's reactivity and compatibility with various synthetic methodologies make it a versatile building block for the preparation of complex organic molecules in academic and industrial settings.
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