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1-bromo-3-(2H3)methoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

873928-72-4

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873928-72-4 Usage

Molecular weight

199.04 g/mol

Type

Deuterated form of 1-bromo-3-methoxybenzene

Hydrogen replacement

Contains one or more hydrogen atoms replaced by deuterium

Usage

Organic synthesis and pharmaceutical research as a reagent or precursor

Industries

Pharmaceuticals, agrochemicals, and material sciences

Physical state

Colorless to pale yellow liquid

Boiling point

239-240°C

Density

1.41 g/cm3

Hazards

Potentially harmful if swallowed, inhaled, or in contact with the skin

Safety measures

Should be handled with proper precautions and safety measures

Check Digit Verification of cas no

The CAS Registry Mumber 873928-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,9,2 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 873928-72:
(8*8)+(7*7)+(6*3)+(5*9)+(4*2)+(3*8)+(2*7)+(1*2)=224
224 % 10 = 4
So 873928-72-4 is a valid CAS Registry Number.

873928-72-4Downstream Products

873928-72-4Relevant academic research and scientific papers

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).

DIHYDROQUINAZOLINE INHIBITORS OF VIRAL TERMINASE

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Paragraph 00191, (2016/08/03)

The present invention relates to new dihydroquinazoline modulators of viral infection, pharmaceutical compositions thereof, and methods of use thereof.

SUBSTITUTED CYCLOHEXANOLS

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Page/Page column 35, (2009/02/11)

Disclosed herein are substituted cyclohexanol opioid receptor modulators and/or neurotransmitter reuptake modulators of Formula I or Formula II, process of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.

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