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4H-Pyrazolo[3,4-d]pyrimidin-4-one, 1,5-dihydro-1-(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65973-99-1

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65973-99-1 Usage

Property

Molecular formula
Content: C11H8N4O3

Property

Derivative
Content: Derivative of pyrazolo[3,4-d]pyrimidin-4-one

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Functional group
Content: 1,5-dihydro-1-(4-nitrophenyl)

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Potential applications
Content: Pharmaceutical research and development possibilities

Property

Use
Content: Starting material in compound synthesis or potential pharmacological properties

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Need for further study
Content: Further research required to understand its full potential and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 65973-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65973-99:
(7*6)+(6*5)+(5*9)+(4*7)+(3*3)+(2*9)+(1*9)=181
181 % 10 = 1
So 65973-99-1 is a valid CAS Registry Number.

65973-99-1Downstream Products

65973-99-1Relevant academic research and scientific papers

Heterocyclic Synthesis Using Hydrazonoyl Halides: Synthesis of Annelated Pyrimidines, Pyridazines and Pyrazoles

Abdelhamid, Abdou O.

, p. 1239 - 1262 (2007/10/02)

Aminocyanopyrazoles and dihydropyrrolopyrazole-4,6-diones were obtained in good yields by the reaction of hydrazonoyl halides with malononitrile and N-arylmaleimides respectively. Pyrazolopyrimidines and pyrazolopyridazines were synthesized in quantitative yields by the reaction of formic acid or formamide and hydrazine hydrate with aminocyanopyrazoles. Novel ring systems, 4-mercapto-1,2,3,5,6,7-hexaazaacenaphthylenes 20 and 7-thia-1,2,4,5,6,10-hexaazacyclopentacenaphthylenes 22 were prepared by the reaction of 18 with carbon disulfide and the reaction of 21 with acetic anhydride. The structures of the products were assigned and confirmed on the basis of their elemental analyses, spectral data and alternate synthesis wherever possible.

3-Chlor-5-dimethylamino-2-formyl-4-aza-2,4-pentadiennitril, Synthese und Umsetzungen mit Nucleophilen

Klemm, Kurt,Pruesse, Wolfgang,Baron, Lothar,Daltrozzo, Ewald

, p. 2001 - 2018 (2007/10/02)

3-Chloro-5-dimethylamino-2-formyl-4-aza-2,4-pentadienenitrile (7) is prepared by partial hydrolysis of the iminium perchlorate 1.In 7 the electrophilic centres (1, 3, 5) regioselectively react with secondary alkylamines, arylamines, and hydrazine derivatives to yield 3-amino-substituted formylazapentadienenitriles and (hydrazonomethyl)azapentadienenitriles.Intramolecular cyclisation leads to triazole betaines, pyrazoles, and 1,4-dihydropyrimidines.

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