76574-39-5 Usage
General Description
2-(2-bromo-6-chlorophenyl)acetonitrile is a chemical compound with the formula C8H5BrClN. It is a white crystalline solid with a molecular weight of 224.49 g/mol. 2-(2-bromo-6-chlorophenyl)acetonitrile is widely used in the pharmaceutical industry as an intermediate for the synthesis of various drugs and pharmaceuticals. It is also used as a reagent in organic synthesis and in the production of agrochemicals. 2-(2-bromo-6-chlorophenyl)acetonitrile is known for its strong odor and should be handled with caution due to its potential toxicity. It is important to handle and use this compound in accordance with proper safety measures.
Check Digit Verification of cas no
The CAS Registry Mumber 76574-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,7 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76574-39:
(7*7)+(6*6)+(5*5)+(4*7)+(3*4)+(2*3)+(1*9)=165
165 % 10 = 5
So 76574-39-5 is a valid CAS Registry Number.
76574-39-5Relevant articles and documents
Copper-catalyzed domino coupling reaction: An efficient method to synthesize oxindoles
Hsieh, Jen-Chieh,Cheng, An-Yi,Fu, Jun-Hao,Kang, Ting-Wei
supporting information; experimental part, p. 6404 - 6409 (2012/09/05)
An efficient and novel procedure for a copper catalyzed domino coupling reaction has been developed, which afforded various oxindoles in good to excellent yields with tolerance of various substituents. In addition, this method could be applied to synthesize horsfiline and coerulescine in few steps with high total yields. The Royal Society of Chemistry 2012.
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.
