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1,3,5-Trichlorobenzene-d3 (CAS# 1198-60-3) is an isotopically labeled research compound that is widely utilized in various scientific and industrial applications due to its unique properties. It is a derivative of trichlorobenzene with three deuterium atoms, which makes it an ideal candidate for research purposes.

1198-60-3

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1198-60-3 Usage

Uses

Used in Research and Development:
1,3,5-Trichlorobenzene-d3 is used as a research compound for the study of chemical reactions and processes. The presence of deuterium atoms in the molecule allows for the investigation of reaction mechanisms, kinetics, and isotope effects, which are crucial for understanding the underlying principles of various chemical phenomena.
Used in Analytical Chemistry:
In the field of analytical chemistry, 1,3,5-Trichlorobenzene-d3 serves as an internal standard or a reference compound for the quantification and identification of target analytes. Its isotopically labeled nature provides a reliable and accurate means of comparing the properties of other compounds, ensuring precise measurements and results.
Used in Environmental Studies:
1,3,5-Trichlorobenzene-d3 is employed as a tracer compound in environmental studies, particularly in the assessment of the fate and transport of pollutants in the environment. Its unique isotopic signature allows researchers to track and monitor the behavior of contaminants, providing valuable insights into their distribution, persistence, and potential impacts on ecosystems.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,3,5-Trichlorobenzene-d3 is utilized as a starting material or an intermediate in the synthesis of various drugs and drug candidates. Its isotopically labeled nature can be advantageous in the development of new drugs, as it can help in the identification of active compounds and the optimization of their pharmacological properties.
Used in Material Science:
1,3,5-Trichlorobenzene-d3 is also used in material science for the development of novel materials with specific properties. Its unique isotopic composition can be exploited to create materials with enhanced performance characteristics, such as improved stability, reactivity, or selectivity, which can be applied in various industrial processes and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1198-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1198-60:
(6*1)+(5*1)+(4*9)+(3*8)+(2*6)+(1*0)=83
83 % 10 = 3
So 1198-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl3/c7-4-1-5(8)3-6(9)2-4/h1-3H/i1D,2D,3D

1198-60-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-trichloro-2,4,6-trideuteriobenzene

1.2 Other means of identification

Product number -
Other names 1,3,5-Trichlorobenzene-d3

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1198-60-3 SDS

1198-60-3Upstream product

1198-60-3Downstream Products

1198-60-3Relevant academic research and scientific papers

Cycloarenes, a New Class of Aromatic Compounds, I. Synthesis of Kekulene

Staab, Heinz A.,Diederich, Francois

, p. 3487 - 3503 (2007/10/02)

Definition and nomenclature of cycloarenes, a new class of aromatic compounds, are discussed.Cyclododecakisbenzene ("kekulene", 1) has been synthesized as the first representative of cycloarenes. - From the dithiaphane 11 by double sulfur extrusion, either photochemically or by pyrolysis of disulfone 12, the carbocyclic system 13 was formed which by dehydrogenation yielded 14.By Stevens rearrangement of 11 followed by elimination the phanediene 15 was obtained which was dehydrogenated to 18.From 15 by photo-cyclodehydrogenation in excellent yield the octahydrokekulene 19 was obtained.The different reactivity of 15 and 18 in the photo-cyclodehydrogenation is discussed in terms of electronic and steric effects.Dehydrogenation of 19 yielded 1.

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