55153-95-2 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(2-bromoethyl)-4-(methylsulfinyl)benzene is used as an organic building block for the creation of various pharmaceutical products. Its unique structure and reactivity allow for the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the development of new medications.
Used in Agrochemical Production:
In the agrochemical industry, 1-(2-bromoethyl)-4-(methylsulfinyl)benzene is utilized as a key component in the synthesis of different agrochemical products. Its role in creating carbon-carbon and carbon-heteroatom bonds is vital for the production of effective and innovative agrochemicals.
Used as a Reagent in Chemical Reactions:
Due to its potential in facilitating the formation of essential chemical bonds, 1-(2-bromoethyl)-4-(methylsulfinyl)benzene is also employed as a reagent in various chemical reactions. This enhances its versatility and value in the field of organic chemistry.
Safety Precautions:
It is important to handle and use 1-(2-bromoethyl)-4-(methylsulfinyl)benzene with care, as it may pose health and environmental hazards if not properly managed. Appropriate safety measures should be taken to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 55153-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,5 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55153-95:
(7*5)+(6*5)+(5*1)+(4*5)+(3*3)+(2*9)+(1*5)=122
122 % 10 = 2
So 55153-95-2 is a valid CAS Registry Number.
55153-95-2Relevant academic research and scientific papers
CYCLIC TERTIARY AMINE COMPOUND
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Referential example 7, (2010/11/08)
The present invention provides a cyclic tertiary amine compound which is capable of inhibiting the production of inflammatory cytokines. It is either a compound having a structure represented by the following general formula (I): (wherein A represents an optionally substituted trivalent group derived from pyrimidine, pyrrole, or the like; R1 represents an aryl or a heteroaryl group which may optionally be substituted; R2 represents a heteroaryl group which may optionally be substituted; and R3 represents a cyclic tertiary amino group) or a pharmacologically acceptable salt of the compound.
