75366-10-8 Usage
Description
1-Bromo-2-bromomethyl-3-methyl-benzene is a chemical compound with the molecular formula C8H8Br2. It is a derivative of benzene with two bromine atoms and a methyl group attached to the benzene ring. 1-Bromo-2-bromomethyl-3-methyl-benzene is a clear, colorless liquid with a strong, pungent odor and is considered hazardous if ingested, inhaled, or in contact with skin and eyes.
Uses
Used in Organic Synthesis:
1-Bromo-2-bromomethyl-3-methyl-benzene is used as an intermediate in organic synthesis for the preparation of various pharmaceuticals and agrochemicals. Its unique structure allows for further chemical reactions and modifications, making it a valuable building block in the synthesis of complex organic molecules.
Used in Chemical Reactions:
1-Bromo-2-bromomethyl-3-methyl-benzene is also used as a reagent in chemical reactions, facilitating specific transformations and providing a pathway to desired products. Its presence can influence the course of a reaction and improve the yield of the target molecule.
Used as a Precursor:
1-Bromo-2-bromomethyl-3-methyl-benzene serves as a precursor to other bromoalkyl derivatives, which are important in various chemical applications. Its ability to be converted into a range of different compounds makes it a versatile starting material in the chemical industry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-Bromo-2-bromomethyl-3-methyl-benzene is used as a key component in the synthesis of certain drugs. Its unique properties enable the development of new medications with specific therapeutic effects.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 1-Bromo-2-bromomethyl-3-methyl-benzene is utilized in the creation of pesticides, herbicides, and other agricultural chemicals. Its role in these applications contributes to the development of effective solutions for crop protection and management.
Safety Precautions:
Due to its hazardous nature, 1-Bromo-2-bromomethyl-3-methyl-benzene should be handled with care and used in a well-ventilated area with appropriate safety precautions to minimize health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 75366-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,6 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75366-10:
(7*7)+(6*5)+(5*3)+(4*6)+(3*6)+(2*1)+(1*0)=138
138 % 10 = 8
So 75366-10-8 is a valid CAS Registry Number.
75366-10-8Relevant articles and documents
Structure Elucidation Using Gas Chromatography-Infrared Spectroscopy/Mass Spectrometry Supported by Quantum Chemical IR Spectrum Simulations
Doetzer, Reinhard,Kulsing, Chadin,Marriott, Philip J.,Nolvachai, Yada,Salzmann, Susanne,Steiner, Sandra,Zavahir, J. Shezmin
, p. 15508 - 15516 (2021/11/23)
An improved strategy for compound identification incorporating gas chromatography hyphenated with Fourier transform infrared spectroscopy and mass spectroscopy (GC-FTIR/MS) is reported. (Over)reliance on MS may lead either to ambiguous identity or to incorrect identification of a compound. However, the MS result is useful to provide a cohort of possible compounds. The IR result for each tentative compound match was then simulated using molecular modeling, to provide functional group and isomer differentiation information, and then compared with the experimental FTIR result, offering identification based on both MS and IR. Several basis sets were evaluated for IR simulations; Def2-TZVPP was a suitable basis set and correlated well with experimental data. The approach was applied to industrial applications, confirming the isomers of 2,3-bis(thiosulfanyl)-but-2-enedinitrile, bromination products of 1-bromo-2,3-dimethylbenzene, and autoxidative degradation of phenyl-di-tert-butylphosphine.
COMPOUNDS
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, (2019/03/15)
The present invention relates to novel compounds, and therapeutically acceptable salts thereof of the formula (I), which inhibit exogenously or endogenously stimulated gastric acid secretion and thus can be used in the prevention and treatment of gastrointestinal inflammatory diseases