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

112906-28-2

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112906-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112906-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,0 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112906-28:
(8*1)+(7*1)+(6*2)+(5*9)+(4*0)+(3*6)+(2*2)+(1*8)=102
102 % 10 = 2
So 112906-28-2 is a valid CAS Registry Number.

112906-28-2Downstream Products

112906-28-2Relevant 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: A NOVEL SYNTHESIS OF 2-THIENYLBIARYLS

Elagamey, Abdel Ghani A.,Sofan, Mamdouh A.,Kandeel, Zaghloul E.,Elnagdi, Mohamed H.

, p. 1561 - 1565 (2007/10/02)

A novel synthesis of 2-thienylbiaryls via the reaction of the 2-cyano-3-(2-thienyl)crotononitrile with cinnamonitriles is reported.The same products were also obtained from the reaction of 1,1-dicyano-2-thienyl-4-arylbuta-1,3-dienes with malononitrile or

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