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7H-1,3,4-Thiadiazolo[3,2-a]pyrimidin-7-one, 2,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82090-63-9

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82090-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82090-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,9 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82090-63:
(7*8)+(6*2)+(5*0)+(4*9)+(3*0)+(2*6)+(1*3)=119
119 % 10 = 9
So 82090-63-9 is a valid CAS Registry Number.

82090-63-9Downstream Products

82090-63-9Relevant academic research and scientific papers

Synthesis of New Condensed Pyrimidine Systems: Reactions of Heterocyclic Amines with Acetylenic Esters

Sahu, J. K.,Dehuri, S. N.,Naik, S.,Nayak, A.

, p. 117 - 120 (2007/10/02)

Several hitherto unreported 1,3,4-oxa/thiadiazolopyrimidin-7-ones (1 and 2) and thiazolopyrimidin-7-ones (3) have been synthesised by the reaction of 2-amino-1,3,4-oxa/thiadiazoles and 2-amino-4-arylthiazoles respectively with ethyl phenylpropiolate.The reaction of these amines with diethyl acetylenedicarboxylate furnishes the 7-oxo-5-carbethoxy derivatives (8-10).A similar reaction of 2-aminobenzothiazole with diethyl acetylenedicarboxylate affords 4-carbethoxypyrimidobenzothiazol-2(H)-one (7).To assign the structures of the 7-oxo derivatives the isomeric 5-oxo-7-carbethoxy derivatives (14) have also been synthesised by an unambiguous route.

SINTESI ED ATTIVITA ANTIMICOTICA DI DERIVATI DELL'1,3,4-TIADIAZOLOPIRIMIDONE

Russo, F.,Santagati, M.,Santagati, A.,Blandino, G.

, p. 983 - 993 (2007/10/02)

As a continuation of previous research designed to obtain derivatives of 1,3,4-thiadiazole of pharmacological interest, some derivatives of 1,3,4-thiadiazolepyrimidin-5-one and isomeric 7-one were prepared.The fungistatic activity of the products was tested in vitro against the following: Candida albicans, Candida parapsilosis, Candida tropicalis, Cryptococcus neoformans and Trichophyton rubrum.No relevant antifungal activity was observed for any of the compounds examined.

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