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N,N-DIMETHYLACETAMIDE-2,2,2-D3, with the CAS number 20255-66-7, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a derivative of N,N-dimethylacetamide, which has a deuterium atom (D) replacing a hydrogen atom, making it a useful tool for investigating the properties and behavior of molecules in different environments.

20255-66-7

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20255-66-7 Usage

Uses

Used in Research and Development:
N,N-DIMETHYLACETAMIDE-2,2,2-D3 is used as an isotopically labeled compound for research purposes. The incorporation of deuterium in the molecule allows for the study of its unique properties and behavior in various chemical reactions and processes. This can be particularly useful in understanding the effects of isotopic substitution on reaction rates, mechanisms, and product formation.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N,N-DIMETHYLACETAMIDE-2,2,2-D3 can be used as a reference compound for the development of new drugs and drug candidates. The isotopically labeled nature of the compound can help researchers identify and optimize the pharmacokinetic and pharmacodynamic properties of potential drug molecules, leading to the discovery of more effective and safer medications.
Used in Chemical Synthesis:
N,N-DIMETHYLACETAMIDE-2,2,2-D3 can also be employed as a starting material or intermediate in the synthesis of various organic compounds. The presence of deuterium in the molecule can provide insights into the reaction pathways and mechanisms, which can be valuable for optimizing synthetic routes and improving the overall yield of the desired products.
Used in Environmental Studies:
In environmental science, N,N-DIMETHYLACETAMIDE-2,2,2-D3 can be utilized as a tracer compound to study the fate and transport of chemicals in the environment. The deuterium label can help differentiate the labeled compound from its non-labeled counterpart, allowing researchers to track its movement and interactions with other environmental components.
Used in Analytical Chemistry:
N,N-DIMETHYLACETAMIDE-2,2,2-D3 can be employed as an internal standard or calibration reference in analytical chemistry. The isotopically labeled compound can be used to improve the accuracy and precision of quantitative measurements, particularly in techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy.

Check Digit Verification of cas no

The CAS Registry Mumber 20255-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,5 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20255-66:
(7*2)+(6*0)+(5*2)+(4*5)+(3*5)+(2*6)+(1*6)=77
77 % 10 = 7
So 20255-66-7 is a valid CAS Registry Number.

20255-66-7SDS

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 N,N-DIMETHYLACETAMIDE-2,2,2-D3

1.2 Other means of identification

Product number -
Other names d3-N,N-Dimethylacetamid

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:20255-66-7 SDS

20255-66-7Downstream Products

20255-66-7Relevant academic research and scientific papers

Direct and Unified Access to Carbon Radicals from Aliphatic Alcohols by Cost-Efficient Titanium-Mediated Homolytic C?OH Bond Cleavage

Suga, Takuya,Takahashi, Yuuki,Miki, Chinatsu,Ukaji, Yutaka

supporting information, (2022/01/31)

Low-valent Ti-mediated homolytic C?O bond cleavage offers unified access to carbon radicals from ubiquitous non-activated tertiary, secondary, and even primary alcohols. In contrast to the representative Ti reagents, which were ineffective for this purpos

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