67197-53-9 Usage
General Description
2-(2,6-dibromophenyl)acetonitrile is a chemical compound with the molecular formula C9H6Br2N. It is a white to off-white crystalline powder that is primarily used as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. 2-(2,6-dibroMophenyl)acetonitrile is known for its ability to act as a building block in the synthesis of various organic molecules due to its unique structure and reactivity. It is important to handle this compound with care as it can cause irritation to the skin, eyes, and respiratory system, and should only be used by trained professionals in a controlled laboratory environment.
Check Digit Verification of cas no
The CAS Registry Mumber 67197-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,1,9 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67197-53:
(7*6)+(6*7)+(5*1)+(4*9)+(3*7)+(2*5)+(1*3)=159
159 % 10 = 9
So 67197-53-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Br2N/c9-7-2-1-3-8(10)6(7)4-5-11/h1-3H,4H2
67197-53-9Relevant articles and documents
An efficient one-pot synthesis of novel 4-aryl-1-methyloxindoles
van den Hoogenband, Adri,Lange, Jos H.M.,Iwema-Bakker, Wouter I.,den Hartog, Jack A.J.,van Schaik, Jord,Feenstra, Rolf W.,Terpstra, Jan Willem
, p. 4361 - 4364 (2006)
An unprecedented synthetic approach to novel 4-aryl-1-methyloxindoles is described. The method involves the intramolecular palladium-catalyzed amidation of N-methyl-2,6-dibromophenylacetamide followed by an in situ Suzuki cross-coupling reaction with a (h
Substituted benzocarbocycles by palladium-catalyzed cascade reactions featuring a C(sp3) - H activation step
Hitce, Julien,Baudoin, Olivier
, p. 2054 - 2060 (2008/09/17)
Valuable 4- and 5-membered benzocarbocycles were synthesized via selective palladium-catalyzed cascade reactions which combined C(sp3)-H activation, Heck cyclization, Heck arylation or olefin hydrogenation. In all cases, all mechanistically independent steps were catalyzed by a single multi-functional catalyst.
