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91265-79-1

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91265-79-1 Usage

Core structure

Thiadiazole

Substituents

Phenyl and Ethyl

Classification

Organic compound

Applications

a. Organic synthesis
b. Medicinal chemistry (building block for pharmaceutical compounds and agrochemical products)
c. Material science (potential applications)
d. Chemical research (potential applications)

Synthesis

The properties and potential uses depend on the exact nature of its synthesis.

Specific applications

Determined by the intended use and synthesis method.

Check Digit Verification of cas no

The CAS Registry Mumber 91265-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91265-79:
(7*9)+(6*1)+(5*2)+(4*6)+(3*5)+(2*7)+(1*9)=141
141 % 10 = 1
So 91265-79-1 is a valid CAS Registry Number.

91265-79-1Relevant articles and documents

Regioselective synthesis of 2-amino-substituted 1,3,4-oxadiazole and 1,3,4-thiadiazole derivatives via reagent-based cyclization of thiosemicarbazide intermediate

Yang, Seung-Ju,Lee, Seok-Hyeong,Kwak, Hyun-Jung,Gong, Young-Dae

, p. 438 - 444 (2013/04/10)

A regioselective, reagent-based method for the cyclization reaction of 2-amino-1,3,4-oxadiazole and 2-amino-1,3,4-thiadiazole core skeletons is described. The thiosemicarbazide intermediate 3 was reacted with EDC·HCl in DMSO or p-TsCl, triethylamine in N-

Mesoionic xanthine analogues: Antagonists of adenosine receptors

Glennon,Tejani-Butt,Padgett,Daly

, p. 1364 - 1367 (2007/10/02)

A variety of mesoionic xanthines including mesoionic thiazolo[3,2-α]pyrimidines, benzothiazolopyrimidines, and 1,3,4-thiadiazolo[3,2-α]pyrimidines were antagonists of A1-adenosine receptors (inhibition of binding of [3H]-cyclohexylad

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