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Thieno[2,3-b]pyridine-2-carbonitrile, 3-amino-4-methyl-6-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52505-66-5

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52505-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52505-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,0 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52505-66:
(7*5)+(6*2)+(5*5)+(4*0)+(3*5)+(2*6)+(1*6)=105
105 % 10 = 5
So 52505-66-5 is a valid CAS Registry Number.

52505-66-5Relevant academic research and scientific papers

Synthesis of thieno[2,3-b]pyridines with an oxalamidic acid or an oxalamidic alkylester residue and of 4-alkoxy-pyrido[3',2':4,5]thieno]3,2-d]pyrimidine-2-carboxylic acid derivatives

Wagner,Leistner,Vieweg,Krasselt,Prantz

, p. 342 - 346 (2007/10/02)

N-(2-Alkoxycarbonyl-thieno[2,3-b]pyrid-3-yl)oxalamide acid alkylester B were synthesized by the reaction of 3-amino-2-carboxylic esters A with oxalic acid diethylester in presence of sodium alkoxides. The 3-amino-2-cyano-thieno[2,3-b]pyridines C yielded under the same conditions via the N- (2-cyano-thieno[2,3-b]pyrid-3-yl)oxalamidic acid alkylesters D/1-D/4 the 4-alkoxy-pyrido[3',2': 4,5]thieno[3,2-d]pyrimidine-2-carboxylic acid alkylesters E/1-E/8. The compounds D/1, D/2 and E/1-E/5 were hydrolyzed to give the corresponding carboxylic acids. The 3-amino-furo[2,3-b]pyridine-2-carboxylic acid ethylester H reacted with oxalic ethylester chloride to give the oxalamide ethylester I. The synthesized substances showed an antianaphylactic activity.

Synthesis and antifungal activity of pyrido[3',2':4,5]thieno[3,2-d]-1,2,3-triazine derivatives

Guerrera,Salerno,Sarva,Siracusa,Oliveri,Minardi

, p. 1725 - 1733 (2007/10/02)

The antimicrobical activity of some pyrido[3'2':4,5]thieno[3,2d]-1,2,3-triazine derivatives has been studied. Some compounds proved effective against microorganisms in vitro, compounds 3a and 3c in particular exhibited antifungal activity, comparable to M

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