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100835-59-4

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100835-59-4 Usage

Description

4-Bromoanisole-d3, also known as p-Methoxyphenyl Bromide-d3 (M265815), is a deuterated compound commonly utilized in the field of chemistry and materials science. It is characterized by the presence of deuterium (D), an isotope of hydrogen, which provides unique properties for various applications.

Uses

Used in Semiconductor Industry:
4-Bromoanisole-d3 is used as a solvent additive for controlling the morphology and crystallization in semiconducting polymer blends. Its deuterated nature allows for enhanced control over the polymer's properties, leading to improved performance in electronic devices.
Used in Chemical Research:
In the field of chemical research, 4-Bromoanisole-d3 serves as a valuable compound for studying reaction mechanisms and understanding the behavior of molecules. The presence of deuterium in the molecule can provide insights into the kinetics and thermodynamics of chemical reactions, making it a useful tool for researchers.
Used in Material Science:
4-Bromoanisole-d3 is also employed in material science as a component in the development of novel materials with specific properties. Its deuterated nature can contribute to the enhancement of material characteristics, such as stability, solubility, and reactivity, which can be beneficial in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 100835-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,3 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100835-59:
(8*1)+(7*0)+(6*0)+(5*8)+(4*3)+(3*5)+(2*5)+(1*9)=94
94 % 10 = 4
So 100835-59-4 is a valid CAS Registry Number.

100835-59-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-[2H3]methoxybenzene

1.2 Other means of identification

Product number -
Other names 1-bromo-4-[2H3]methoxybenzene

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:100835-59-4 SDS

100835-59-4Relevant articles and documents

Preparation method of nitrogen-alkyl (deuterated alkyl) aromatic heterocycle and alkyl (deuterated alkyl) aryl ether compound

-

Paragraph 0093-0098, (2021/04/03)

The invention provides a method for preparing nitrogen-alkyl(deuterated alkyl)aromatic heterocycle and alkyl(deuterated alkyl)aryl ether compounds. The method adopted in the invention specifically comprises the following steps: firstly, adding an alkoxy base (MOR') or a combination reagent Q (comprising a base M'X, an alcohol C and a molecular sieve E) into a solvent B to be stirred; then, addingan aromatic compound D of nitrogen sulfonyl or oxygen sulfonyl into a mixture; separating and purifying after reaction to obtain nitrogen-alkyl(deuterated alkyl)aromatic heterocycle or alkyl(deuterated alkyl)aryl ether. The method can realize one-step conversion from an electron withdrawing benzenesulfonyl protecting group on a nitrogen or oxygen atom to an electron donating alkyl protecting group, avoids using highly toxic alkyl halide, and has advantages of being efficient, economical, environmentally friendly, mild in condition, good in substrate universality and high in yield; the prepareddeuterated compounds can be widely applied to the fields of pharmaceutical chemistry and organic chemistry synthesis.

Trideuteromethylation Enabled by a Sulfoxonium Metathesis Reaction

Shen, Zuyuan,Zhang, Shilei,Geng, Huihui,Wang, Jiarui,Zhang, Xinyu,Zhou, Anqi,Yao, Cheng,Chen, Xiaobei,Wang, Wei

supporting information, p. 448 - 452 (2019/01/14)

A conceptually novel sulfoxonium metathesis reaction between TMSOI and cost-effective DMSO-d6 is developed for the efficient generation of a new trideuteromethylation reagent TDMSOI. The new reagent TDMSOI is produced highly efficiently by simply heating a mixture of TMSOI and DMSO-d6 and directly used for subsequent trideuteromethylation in a "one-pot" operation. The preparative power of the new versatile reagent and the "one-pot" protocol is demonstrated by its use to install the ?CD3 moiety into broad functionalities including phenols, thiophenols, acidic amines, and enolizable methylene units in high yield and at a useful level of deuteration (>87% D).

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