17815-88-2 Usage
Description
[bromo(fluoro)methyl]benzene, with the molecular formula C7H6BrF and a molecular weight of 189.022 g/mol, is a colorless liquid characterized by a sweet odor. It is a haloalkane that contains both bromine and fluorine atoms, making it a versatile compound in the realm of organic synthesis. As a reagent and intermediate, it plays a significant role in the production of pharmaceuticals and agrochemicals. However, it is essential to handle this hazardous substance with care due to its potential for causing skin and eye irritation and its harmful effects if ingested or inhaled.
Uses
Used in Organic Synthesis:
[bromo(fluoro)methyl]benzene is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions. Its unique combination of bromine and fluorine atoms allows it to participate in a wide range of reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, [bromo(fluoro)methyl]benzene is utilized as an intermediate in the production of various drugs. Its presence in the synthesis process can contribute to the development of new medications with improved efficacy and reduced side effects.
Used in Agrochemical Production:
[bromo(fluoro)methyl]benzene also finds application in the agrochemical sector, where it is employed as an intermediate in the synthesis of pesticides and other agricultural chemicals. Its role in this industry is crucial for the development of effective and environmentally friendly products to protect crops and enhance agricultural productivity.
Safety Measures:
Given the hazardous nature of [bromo(fluoro)methyl]benzene, it is imperative to implement appropriate safety measures during its handling and use. This includes wearing personal protective equipment (PPE) such as gloves, goggles, and masks to minimize the risk of skin and eye irritation, as well as inhalation of the compound. Additionally, proper storage and disposal protocols should be followed to ensure the safety of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 17815-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,1 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17815-88:
(7*1)+(6*7)+(5*8)+(4*1)+(3*5)+(2*8)+(1*8)=132
132 % 10 = 2
So 17815-88-2 is a valid CAS Registry Number.
17815-88-2Relevant articles and documents
Moss,Przybyla
, p. 647 (1969)
FLP-Catalyzed Monoselective C-F Functionalization in Polyfluorocarbons at Geminal or Distal Sites
Gupta, Richa,Mandal, Dipendu,Jaiswal, Amit K.,Young, Rowan D.
, p. 1915 - 1920 (2021/04/05)
We report frustrated Lewis pair (FLP)-catalyzed monoselective C-F activation in a range of aliphatic polyfluorocarbons with equivalent geminal and distal C-F positions. This methodology can be applied to aromatic-, ether-, thioether-, and alkyl-supported fluoromethyl groups. We expand the range of FLP base partners that work with monoselective C-F activation to include sulfide. The activated products can be subsequently functionalized via SN2 substitutions, photoredox-alkylations, and Suzuki couplings.
C-ARYL GLYCOSIDE COMPOUNDS FOR THE TREATMENT OF DIABETES AND OBESITY
-
Page/Page column 78-79, (2009/10/30)
This invention relates to a compound of generic formula (I): (I) as well as a pharmaceutically acceptable salt thereof, a tautomer, optical isomer or a mixture of optical isomers in any proportion, in particular a mixture of enantiomers, and particularly a racemate mixture, in particular for use thereof as a drug, notably in the treatment of diabetes.
