916596-02-6 Usage
General Description
3-Chloro-4-ethoxybenzonitrile is a chemical compound with the molecular formula C9H8ClNO. It is a chloro-substituted benzonitrile derivative that is commonly used as an intermediate in the synthesis of various organic compounds. It has several industrial applications, including its use as a building block in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. The presence of both the chloro and ethoxy groups makes it a versatile starting material for the synthesis of a wide range of compounds. It is important to handle this chemical with care, as it may be harmful if ingested, inhaled, or comes into contact with the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 916596-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,5,9 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 916596-02:
(8*9)+(7*1)+(6*6)+(5*5)+(4*9)+(3*6)+(2*0)+(1*2)=196
196 % 10 = 6
So 916596-02-6 is a valid CAS Registry Number.
InChI:InChI=1S/C9H8ClNO/c1-2-12-9-4-3-7(6-11)5-8(9)10/h3-5H,2H2,1H3
916596-02-6Relevant articles and documents
COMPOUNDS AND USES THEREOF
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Page/Page column 182, (2018/05/17)
The present invention features compounds useful in the treatment of neurological disorders. The compounds of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological disorders.
Ruthenium-catalyzed intramolecular selective halogenation of O-methylbenzohydroximoyl halides: A new route to halogenated aromatic nitriles
Chinnagolla, Ravi Kiran,Pimparkar, Sandeep,Jeganmohan, Masilamani
supporting information, p. 3146 - 3148 (2013/06/04)
The intramolecular halogenation of O-methylbenzohydroximoyl halides in the presence of a Ru catalyst and the ligand diphenylacetylene afforded halo substituted aromatic nitriles in a highly regioselective manner. Further, substituted nitriles were converted into substituted tetrazole derivatives in the presence of NaN3 and I2.
