131379-38-9 Usage
General Description
Zinc, bromo[3-(ethoxycarbonyl)phenyl]- is a chemical compound that consists of a zinc atom bound to a bromine atom and a phenyl group with an ethoxycarbonyl substituent. Zinc, bromo[3-(ethoxycarbonyl)phenyl]- is commonly used in organic synthesis as a reagent for various reactions due to its ability to promote specific transformations. It is often utilized in the preparation of pharmaceuticals, agrochemicals, and other important chemicals. Additionally, zinc, bromo[3-(ethoxycarbonyl)phenyl]- has been studied for its potential therapeutic properties, particularly in the treatment of certain diseases and disorders. Overall, this compound plays a crucial role in the field of organic chemistry and has a wide range of practical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 131379-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,7 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 131379-38:
(8*1)+(7*3)+(6*1)+(5*3)+(4*7)+(3*9)+(2*3)+(1*8)=119
119 % 10 = 9
So 131379-38-9 is a valid CAS Registry Number.
131379-38-9Relevant articles and documents
Synthesis of Symmetrical Diaryl Ketones by Cobalt-Catalyzed Reaction of Arylzinc Reagents with Ethyl Chloroformate
Rérat, Alice,Michon, Christophe,Agbossou-Niedercorn, Francine,Gosmini, Corinne
, p. 4554 - 4560 (2016/09/23)
Symmetrical diaryl ketones were prepared by a cross-coupling reaction between aryl bromides and ethyl chloroformate. This new method, which uses a catalyst composed of CoBr2and a bipyridine ligand along with readily available starting materials, allows for the synthesis of a variety of symmetrical diaryl ketones in moderate to excellent yields (37–99 %) under mild conditions. This reaction, in which ethyl chloroformate acts as a surrogate of carbon monoxide in the presence of cobalt and zinc, represents an interesting alternative to previously known approaches for the synthesis of diarylmethanones.
Microwave-assisted Negishi and Kumada cross-coupling reactions of aryl chlorides
Walla, Peter,Kappe, C. Oliver
, p. 564 - 565 (2007/10/03)
Rapid Pd or Ni-catalyzed microwave-accelerated Negishi and Kumada cross-coupling reactions of aryl chlorides in solution and on solid phase are reported.
