2317-22-8 Usage
Uses
Used in Chemical Synthesis:
2,6-Dicyanotoluene is used as a chemical intermediate for the synthesis of E-2-(2,6-dicyanophenyl)-N,N-dimethylethenamine. This synthesis involves a condensation reaction with dimethylformamide dimethyl acetal (DMFDMA), which is an important step in the production of various organic compounds.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 2,6-dicyanotoluene can also be used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the creation of a wide range of molecules with potential therapeutic applications.
Used in Dye Industry:
2,6-Dicyanotoluene can be utilized in the dye industry for the production of various dyes and pigments. Its cyano groups can be used to create a range of colors through chemical reactions, making it a valuable component in the development of new dyes.
Used in Polymer Industry:
In the polymer industry, 2,6-dicyanotoluene can be used as a monomer in the production of polymers with specific properties. Its cyano groups can be involved in various polymerization reactions, leading to the creation of polymers with unique characteristics and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2317-22-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2317-22:
(6*2)+(5*3)+(4*1)+(3*7)+(2*2)+(1*2)=58
58 % 10 = 8
So 2317-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N2/c1-7-8(5-10)3-2-4-9(7)6-11/h2-4H,1H3
2317-22-8Relevant articles and documents
Design and synthesis of a trifunctional chiral porphyrin with C2 symmetry as a chiral recognition host for amino acid esters
Mizutani, Tadashi,Ema, Tadashi,Tomita, Takashi,Kuroda, Yasuhisa,Ogoshi, Hisanobu
, p. 4240 - 4250 (2007/10/02)
An intrinsic chiral recognition host, (R,R)- or (S.S)-[trans-5,15-bis(2-hydroxyphenyl)-10-{2,6-bis((methoxycarbonyl)m ethyl)phenyl}-2,3,17,18-tetraethylporphyrinato]zinc(II) (1), was synthesized by the coupling between (3,3',4,4'-tetraethyl-5,5'-bis(α-hyd
Directed Ortho Lithiation of Isophthalonitrile. New Methodology for the Synthesis of 1,2,3-Trisubstituted Benzenes
Krizan, Timothy D.,Martin, J. C.
, p. 2681 - 2682 (2007/10/02)
The lithiation of 1,3-dicyanobenzene with lithium diisopropylamide occurs in high yield, regiospecifically at the 2-position, to give aryllithium species stable at temperatures below -90 deg C.
Syntheses of Dihydropyrenes with Functionality in the Cavity of the ?-Electron Cloud
Mao, Yuh-lin,Boekelheide, Virgil
, p. 2746 - 2749 (2007/10/02)
The cyano group is shown to be a good group for directing ortho lithiation and, with 2,6-dicyanotoluene as starting material, ortho lithiation provides easy access to a variety of 1,2,3-trisubstituted benzene derivatives.The use of such derivatives in the standard thiacyclophane synthesis of dihydropyrenes has provided in good yield trans-15-(4'-butenyl)-16-methyldihydropyrene (14a) and trans-15-(methoxyethyl)-16-methyldihydropyrene (14b), the first examples of dihydropyrenes having functionality within the cavity of the aromatic ?-electron cloud.
