341529-06-4 Usage
Appearance
White solid
Molecular weight
265.06 g/mol
Usage
Intermediate in the synthesis of pharmaceuticals and agrochemicals
Structure
Halogenated imidazole
Application
Useful in organic synthesis and medicinal chemistry
Unique properties
Presence of bromine and fluorine atoms
Chemical reactions
Suitable for various chemical reactions and applications
Safety
Handle with care due to potential health and environmental hazards
Check Digit Verification of cas no
The CAS Registry Mumber 341529-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,1,5,2 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 341529-06:
(8*3)+(7*4)+(6*1)+(5*5)+(4*2)+(3*9)+(2*0)+(1*6)=124
124 % 10 = 4
So 341529-06-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H7BrF2N2/c11-10(12,13)15-7-6-14-9(15)8-4-2-1-3-5-8/h1-7H
341529-06-4Relevant articles and documents
Heteroaryl-N-difluoromethyltrimethylsilanes - Versatile sources of heteroaryl-N-difluoromethyl anions in reactions with carbonyl compounds
Bissky,Staninets,Kolomeitsev,R?schenthaler
, p. 374 - 378 (2007/10/03)
An efficient procedure for synthesizing heteroaryl-N-difluoromethyltrimethylsilanes - new nucleophilic difluoromethylene synthons - from easily available N-bromodifluoromethylated heterocycles, chlorotrimethylsilane and aluminium powder in triglyme or N-methylpyrrolidinone on a preparative scale in 71-75% isolated yield is described. Heteroaryl-N-difluoromethyltrimethylsilanes and benzaldehyde react under fluoride ion catalysis to give 1-(1,1-difluor-2-hydroxy-2-phenyl-ethyl)heteroaryls, whereas for anionic heteroaryl-N-difluoromethylation of cyclohexanone a stoichiometrical mixture of heteroaryl-N-difluoromethyltrimethylsilanes and tetramethylammonium fluoride has to be used.
