189338-32-7 Usage
General Description
4-Carboxy-3,5-dichlorobenzotrifluoride is a chemical compound with the molecular formula C8H2Cl2F3O2. It is a white crystalline solid that is mainly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 4-Carboxy-3,5-dichlorobenzotrifluoride is also utilized in the production of specialty polymers and as a building block in organic synthesis. 4-Carboxy-3,5-dichlorobenzotrifluoride is a fluorinated aromatic compound, which makes it valuable in the development of highly functionalized molecules for various applications. It is important to handle this chemical with caution, as it may have hazardous properties if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 189338-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,3,3 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 189338-32:
(8*1)+(7*8)+(6*9)+(5*3)+(4*3)+(3*8)+(2*3)+(1*2)=177
177 % 10 = 7
So 189338-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H3Cl2F3O2/c9-4-1-3(8(11,12)13)2-5(10)6(4)7(14)15/h1-2H,(H,14,15)
189338-32-7Relevant articles and documents
CARBOCYCLIC GLYT1 RECEPTOR ANTAGONISTS
-
Page/Page column 19, (2011/04/14)
The present invention relates to the use of a compound of formula I wherein R1, R2, R3, R4, X and n are as defined herein or to a pharmaceutically acceptable acid addition salt, to a racemic mixture, or to its corresponding enantiomers and/or optical isomers for the treatment of psychoses, pain, dysfunction in memory and learning, attention deficit, schizophrenia, dementia disorders or Alzheimer's disease.
Metalation and derivatization of all six dichlorobenzotrifluorides: Site selectivities
Masson, Eric,Marzi, Elena,Cottet, Fabrice,Bobbio, Carla,Schlosser, Manfred
, p. 4393 - 4400 (2007/10/03)
The metalation of 2,3-, 2,6-, 2,4- and 3,5-dichlorobenzotrifluorides can be readily effected with standard reagents such as lithium diisopropylamide, lithium 2,2,6,6-tetramethylpiperidide, and butyllithium at the chlorine-adjacent 4- and 3-positions and t
