174913-11-2 Usage
General Description
3-Bromo-2-chloroanisole is a chemical compound with the molecular formula C7H6BrClO. It is an organic compound classified as a chloroanisole, which is a class of chemical compounds used in the production of pharmaceuticals, dyes, and perfumes. 3-Bromo-2-chloroanisole is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is a colorless to pale yellow liquid with a sweet, aromatic odor and is soluble in organic solvents such as ethanol and benzene. The compound is generally used in research and development for the creation of new drugs and can also be used in the production of fragrances and flavors. Its chemical structure consists of a phenyl ether with bromine and chlorine substituents, which give it its unique properties and potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 174913-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,9,1 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 174913-11:
(8*1)+(7*7)+(6*4)+(5*9)+(4*1)+(3*3)+(2*1)+(1*1)=142
142 % 10 = 2
So 174913-11-2 is a valid CAS Registry Number.
174913-11-2Relevant articles and documents
Induction of Axial Chirality in 8-Arylquinolines through Halogenation Reactions Using Bifunctional Organocatalysts
Miyaji, Ryota,Asano, Keisuke,Matsubara, Seijiro
, p. 9996 - 10000 (2017)
The enantioselective syntheses of axially chiral heterobiaryls were accomplished through the aromatic electrophilic halogenation of 3-(quinolin-8-yl)phenols with bifunctional organocatalysts that control the molecular conformations during successive halogenations. Axially chiral quinoline derivatives, which have rarely been synthesized in an enantioselective catalytic manner, were afforded in moderate-to-good enantioselectivities through bromination, and an analogous protocol also enabled enantioselective iodination. In addition, this catalytic reaction, which allows enantioselective control through the use of mono-ortho-substituted substrates, allowed the asymmetric synthesis of 8-arylquinoline derivatives bearing two different halogen groups in high enantioselectivities.
