113508-13-7 Usage
Appearance
Yellow crystalline solid A description of the compound's physical form and color, indicating that it forms solid crystals with a yellow hue.
Solubility
Insoluble in water, soluble in organic solvents A property that describes the compound's ability to dissolve in different types of solvents, with water being a non-solvent and various organic solvents being effective for dissolution.
Chemical structure
Nitrile derivative with a nitro functional group and a chlorine atom attached to a phenyl ring A description of the compound's molecular structure, highlighting the presence of a nitrile group (C≡N), a nitro group (-NO2), and a chlorine atom (Cl) on a phenyl ring (C6H5).
Uses
Intermediate in the synthesis of pharmaceuticals and agrochemicals A property that describes the compound's primary applications, as it is commonly used as a starting material or building block in the production of various drugs and agricultural chemicals.
Toxicity and irritancy
Potential toxic and irritant properties A warning about the compound's potential hazards, emphasizing that it may cause harm or irritation upon contact or exposure, and that proper precautions should be taken when handling and using it.
Check Digit Verification of cas no
The CAS Registry Mumber 113508-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,0 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113508-13:
(8*1)+(7*1)+(6*3)+(5*5)+(4*0)+(3*8)+(2*1)+(1*3)=87
87 % 10 = 7
So 113508-13-7 is a valid CAS Registry Number.
113508-13-7Relevant articles and documents
Specific ortho-Cyanomethylation of Nitroarenes via the Vicarious Nucleophilic Substitution of Hydrogen
Makosza, Mieczyslaw,Wenaell, Maria,Golinski, Miroslaw,Kinowski, Andrzej
, p. 427 - 432 (2007/10/02)
The vicarious nucleophilic substitution of hydrogen in nitroarenes with acetonitrile derivatives XCH2CN in t-BuOK/THF base/solvent system proceeds exclusively ortho to the nitro group.Strong influence of substituents Z in 3-Z-nitrobenzene derivatives on the orientation has been observed.
