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2-amino-4-(furan-2-yl)-6-(thiophen-2-yl)isophthalonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115802-03-4

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115802-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115802-03-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,0 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115802-03:
(8*1)+(7*1)+(6*5)+(5*8)+(4*0)+(3*2)+(2*0)+(1*3)=94
94 % 10 = 4
So 115802-03-4 is a valid CAS Registry Number.

115802-03-4Downstream Products

115802-03-4Relevant academic research and scientific papers

A Simple and Clean Synthesis of Polysubstituted 2,6-Dicyanoanilines Catalyzed by KF/alumina

Jain, Shubha,Keshwal, Balwant S.,Rajguru, Deepika,Bhagwat, Vasant W.

, p. 712 - 715 (2013/03/29)

A simple and clean synthesis of polysubstituted 2,6-dicyanoanilines has been developed via the reaction of arylidenemalonodinitriles with 1-arylethylidenemalonodinitriles in ethanol catalyzed by KF/ alumina. Use of non-hazardous solid base as a catalyst,

Synthesis and antiradiation activity of some sulfur containing thiophene derivatives

Hassan,Ghorab,Nassar

, p. 77 - 86 (2007/10/03)

Condensation of 2-(2,2-dicyano-1-methylvinyl)thiophene (2) with phenylhydrazine furnished the corresponding 2-(1-phenylhydrazonoethyl)-thiophene (4). Compound (4) was obtained also via reaction of (1) with phenylhydrazine. Reaction of (2) with amines gave 2-(2,2-dicyano-1-ethylamino or benzylamino-1 methylethyl)thiophene (5a,b). Treatment of (2) with elemental sulfur yielded directly the cyclised product 2-(5-amino-4-cyano-3-thienyl)thiophene (6). On the other hand refluxing (2) in pyridine with carbon disulfide gave the pyridine-1,3-dithione derivative (7). Condensation of (2) with phenyl isocyanate and/or phenyl isothiocyanate afforded 6-amino-4-(2-thienyl)-1,2-dihydro-2-oxo-1-phenylpyridine-5-carbonitrile (9) and/or 5-(2-thienyl)-2,7-dithioxo-3,8-N-phenyl-1,2,3,7,8-pentahydropyrido[2,3-d] pyrimidine-4-imine (11). Also the dicyano derivative (2) when reacted with cinnamonitrile (12) afforded the 2-(3-amino-2,4-dicyano-5-arylphenyl)-thiophenes (15a-d). Conversion of (15b) into the polyazanaphthalene (17) and (18) was affected via cyclocondensation with phenyl isocyanate and/or phenyl isothiocyanate. Compound (15a) showed promising antiradiation activity.

Nitriles in Organic Synthesis. The Chemical Behavior of - and malononitriles

El-Maghraby, Mohamed Abdallah,Sadek, Kamal Usef,Selim, Maghraby Ali,Elnagdi, Mohamed Hilmy

, p. 1375 - 1378 (2007/10/02)

The chemical behavior of - and malononitriles 1a and b toward electrophilic reagents, active methylene reagents and (arylmethylene)malononitriles is described.

Nitriles in Organic Synthesis: Synthesis of Polysubstituted Anilines and Cyclohexenones

Elagamey, Abdel-Ghani Ali

, p. 766 - 768 (2007/10/02)

Crotononitriles (I) react with cinnamonitriles (III) to afford anilines (IV), ylidenes (VI) or cyclohexenones (VIII).The nature of the end products in these reactions depends on the nature of the reactants and the reaction conditions.

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