100960-68-7 Usage
Uses
Used in Pharmaceutical Industry:
4-chloro-2-methoxybenzonitrile is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure and reactivity contribute to the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 4-chloro-2-methoxybenzonitrile is utilized as an intermediate in the production of agrochemicals. Its properties allow for the creation of effective compounds for agricultural applications.
Used in Organic Synthesis:
4-chloro-2-methoxybenzonitrile is employed as a reagent in organic synthesis, facilitating the formation of complex organic molecules. Its presence in reactions can lead to the production of a variety of organic compounds for different uses.
Used in Medicinal Chemistry Research:
Due to its structural features and potential biological activity, 4-chloro-2-methoxybenzonitrile may be used in medicinal chemistry research. It can be explored for its possible role in the development of new therapeutic agents or for understanding its interactions with biological systems.
Proper handling and storage of 4-chloro-2-methoxybenzonitrile are crucial to ensure the safety of workers and the environment, given its use in various chemical and research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 100960-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,6 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100960-68:
(8*1)+(7*0)+(6*0)+(5*9)+(4*6)+(3*0)+(2*6)+(1*8)=97
97 % 10 = 7
So 100960-68-7 is a valid CAS Registry Number.
100960-68-7Relevant articles and documents
Ligand-Promoted Non-Directed C?H Cyanation of Arenes
Liu, Luo-Yan,Yeung, Kap-Sun,Yu, Jin-Quan
supporting information, p. 2199 - 2202 (2019/01/24)
This article reports the first example of a 2-pyridone accelerated non-directed C?H cyanation with an arene as the limiting reagent. This protocol is compatible with a broad scope of arenes, including advanced intermediates, drug molecules, and natural products. A kinetic isotope experiment (kH/kD=4.40) indicates that the C?H bond cleavage is the rate-limiting step. Also, the reaction is readily scalable, further showcasing the synthetic utility of this method.
Pd(OAc)2-catalyzed alkoxylation of arylnitriles via sp 2 C-H bond activation using cyano as the directing group
Li, Wu,Sun, Peipei
, p. 8362 - 8366 (2013/01/15)
A Pd(OAc)2-catalyzed ortho-alkoxylation of arylnitrile was described. Using cyano as a directing group, the aromatic C-H bond can be functionalized efficiently to generate ortho-alkoxylated arylnitrile derivatives with moderate yields. The opti
HETEROCYCLIC KINASE INHIBITORS
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Page 81, (2010/02/08)
Compounds having the formula (I) are useful for inhibiting protein kinases. Also disclosed are methods of making the compounds, compositions containing the compounds, and methods of treatment using the compounds.
