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1-ethyl-6,7-dimethyl-5-amino-4-oxo-3-phenyl-3,4-dihydrophthalazine-1,6,7-tricarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

173605-15-7

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173605-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173605-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,6,0 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 173605-15:
(8*1)+(7*7)+(6*3)+(5*6)+(4*0)+(3*5)+(2*1)+(1*5)=127
127 % 10 = 7
So 173605-15-7 is a valid CAS Registry Number.

173605-15-7Downstream Products

173605-15-7Relevant academic research and scientific papers

Alkyl(oxo)pyridazinecarbonitriles as Bnilding Blocks in Heterocyclic Synthesis: Novel Syntheses of Pyridopyridazines, Pyridopyridazines, Thiopyranopyridazines and 1,3,4-thiadiazaacenaphthylenes

Abu-Shanab, Fathi A.,Wakefield, Basil,Al-Omran, Fatima,Khalek, Mervat M. Abdel,Elnagdi, Mohamed Hilmy

, p. 2924 - 2946 (2007/10/03)

The pyridopyridazines 4a-k were obtained via condensing the pyridazinones 1a,b with dimethylformamide dimethyl acetal and subsequent treatment of the formed dimethylaminoethylene derivatives (2a-c) with ammonia, amines and hydrazines.Compound 4a is also formed from the reaction of 1d with HOAc/HCl (cf.Scheme 1).In contrast 2a-c afforded the pyridopyridazine-1-carboxylic acid 6a-c on treatment with HOAc/HCl.The reaction of 1a with carbon disulfide followed by methyl iodide gives the thiopyranopyridazine 11.The reaction of the thienopyridazinone (13a) with dimethylacetylene dicarboxylate gives the phthalazine (16) as the sole product, whereas reaction of (13a) with diethyl fumarate gives the thiadiazaacenaphthylene (19).

STUDIES WITH POLYFUNCTIONALLY SUBSTITUTED HETEROAROMATICS: NEW ROUTES FOR SYNTHESIS OF BENZOAZINES

Negm, Abdalla M.,El-Aal, Fatma Abd El-Maksoud Abd,Hafez, Ebtisam A.,Elnagdi, Mohamed H.,Mostafa, Yasser M. N.

, p. 1 - 8 (2007/10/03)

Pyridazine (I) reacts with dimethyl acetylenedicarboxylate and with N-phenyl-maleimide yielding phthalazine (II) and pyrrolophthalazine (III), respectively.Pyridine IV reacts with benzylidene malononitrile to give compound VI.Compounds VIa-c could be successfully converted into the isoquinolines XIa-c on treatment with acrylonitrile.In contrast to the behavior of arylidene malononitrile, compound IV react with N-phenylmaleimide to yield the pyrroloisoquinoline XIII.Similarly, the reaction of compound IV with each of tetracyanoethylene and dimethyl acetylenecarboxylate gave compounds XIV and XV respectively.Key words: Phthalazine, pyrrolophthalazine, isoquinoline, pyrroloisoquinoline, pyridothienopyridine.

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