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1861-01-4

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1861-01-4 Usage

Description

ETHYL-ALPHA,ALPHA-D2-BENZENE, with the CAS number 1861-01-4, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. Its unique isotopic labeling allows for the tracking and analysis of specific chemical reactions and processes, making it a valuable tool in the field of chemistry and related disciplines.

Uses

Used in Chemical Research:
ETHYL-ALPHA,ALPHA-D2-BENZENE is used as a research compound for studying chemical reactions and processes. Its isotopic labeling enables scientists to track and analyze specific pathways and mechanisms, providing valuable insights into the behavior of molecules and their interactions.
Used in Pharmaceutical Development:
In the pharmaceutical industry, ETHYL-ALPHA,ALPHA-D2-BENZENE serves as a crucial component in the development of new drugs and therapies. Its isotopic labeling allows researchers to investigate the effects of potential drug candidates on biological systems, aiding in the design and optimization of more effective and targeted treatments.
Used in Environmental Studies:
ETHYL-ALPHA,ALPHA-D2-BENZENE is also employed in environmental research, where it can be used to study the fate and transport of pollutants in the environment. Its isotopic labeling helps researchers to trace the movement and transformation of contaminants, contributing to a better understanding of their impact on ecosystems and human health.
Used in Analytical Chemistry:
In the field of analytical chemistry, ETHYL-ALPHA,ALPHA-D2-BENZENE is used as a reference material or internal standard for various analytical techniques. Its isotopic labeling provides a reliable and accurate means of calibrating instruments and validating analytical methods, ensuring the precision and reliability of experimental results.

Check Digit Verification of cas no

The CAS Registry Mumber 1861-01-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1861-01:
(6*1)+(5*8)+(4*6)+(3*1)+(2*0)+(1*1)=74
74 % 10 = 4
So 1861-01-4 is a valid CAS Registry Number.

1861-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dideuterioethylbenzene

1.2 Other means of identification

Product number -
Other names Ethyl-1,1-d2-benzene

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:1861-01-4 SDS

1861-01-4Relevant articles and documents

A Convenient and Selective Method for Reductive Deuteriation of Aryl Carbonyl Compounds

Ofosu-Asante, Kofi,Stock, Leon M.

, p. 2938 - 2939 (1987)

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Room-Temperature Palladium-Catalyzed Deuterogenolysis of Carbon Oxygen Bonds towards Deuterated Pharmaceuticals

Ou, Wei,Xiang, Xudong,Zou, Ru,Xu, Qing,Loh, Kian Ping,Su, Chenliang

supporting information, p. 6357 - 6361 (2021/02/16)

Site-specific incorporation of deuterium into drug molecules to study and improve their biological properties is crucial for drug discovery and development. Herein, we describe a palladium-catalyzed room-temperature deuterogenolysis of carbon–oxygen bonds

Synthesis method of aryl deuterated methane

-

Paragraph 0065-0066; 0085-0090, (2020/06/15)

The invention discloses a synthesis method of aryl deuterated methane, and relates to the technical field of organic synthesis. The synthesis method of aryl deuterated methane comprises the followingstep: reacting ketone with deuterium gas in the presence

Selective sp3 C-H bond activation of alkylaromatics promoted by platinum complexes

Miyashita, Akira,Hotta, Masatoshi,Saida, Yoshiko

, p. 353 - 358 (2007/10/02)

Facile sp3 C-H bond activation of toluene, p-xylene and mesitylene, was photochemically promoted by trans-Pt(CH2CMe2Et)Br(PPh3)2 leading to trans-Pt(CH2Ar)Br(PPh3)2 quantitatively, while regioselective sp3 C-H bond cleavage at the benzylic position of ethylbenzene and cumene readily took place to yield styrene and α-methylstyrene, respectively.A possible reaction mechanism involving radical process is discussed on the basis of isotope and radical-trap experiments. Key words: Platinum; Benzyl; Bond activation; Radical; Photochemistry

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