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1-methyl-3-[(phenyl)-(phenylimino)methyl]thiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70375-39-2

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70375-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70375-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,7 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70375-39:
(7*7)+(6*0)+(5*3)+(4*7)+(3*5)+(2*3)+(1*9)=122
122 % 10 = 2
So 70375-39-2 is a valid CAS Registry Number.

70375-39-2Relevant academic research and scientific papers

Synthesis and biological evaluation of a new series of 2,3,5-substituted [1,2,4]-thiadiazoles as modulators of adenosine A1 receptors and their molecular mechanism of action

G?bly?s, Anikó,De Vries, Henk,Brussee, Johannes,Ijzerman, Adriaan P.

, p. 1145 - 1151 (2007/10/03)

We synthesized two series (7a-i and 8a-i) of 2,3,5-substituted [1,2,4]-thiadiazole analogues of SCH-202676 (7a, 2,3-diphenyl-5-N-methylimino- 2H-[1,2,4]-thiadiazole) with emphasis on the N-imino substituent. Compounds 7a-g,i and 8a-g at a final concentrat

Synthesis and Biological Evaluation of 2,3,5-Substituted [1,2,4]Thiadiazoles as Allosteric Modulators of Adenosine Receptors

Van Den Nieuwendijk, Adrianus M. C. H.,Pietra, Daniele,Heitman, Laura,G?bly?s, Anikó,IJzerman, Adriaan P.

, p. 663 - 672 (2007/10/03)

A number of 2,3,5-substituted [1,2,4]thiadiazole analogues of SCH-202676 (N-(2,3-diphenyl-[1,2,4]thiadiazole-5(2H)-ylidene)methanamine, 7a) were synthesized and tested as potential allosteric modulators of adenosine receptors. All compounds were capable of displacing the binding of the radiolabeled agonist [3H]CCPA to human A1 adenosine receptors, whereas modest and varying effects were observed on the binding of [3H]DPCPX, a radiolabeled antagonist for this receptor subtype. Four compounds, 7a (SCH-202676), 7k (LUF5792), 71 (LUF5794), and 8e (LUF5789), were selected for more detailed characterization. They all proved allosteric inhibitors of agonist binding, with 7k being most potent, whereas their effects on antagonist binding were more ambiguous. Subsequently, experiments were done on human adenosine A2A and A3 receptors. Compounds 7a and 7l displayed peculiar displacement characteristics of both radiolabeled agonist and antagonist binding to A2A receptors, whereas 7a showed some activity on A3 receptors.

Cycloaddition of N-(2,2,2-trichloroethylidene)-substituted carboxamides and carbamates to 1,2,4-thiadiazol-5(2H)-imines

Zyabrev, Vladimir S.,Rensky, Mikhail A.,Rusanov, Eduard B.,Drach, Boris S.

, p. 474 - 480 (2007/10/03)

1,2,4-Thiadiazol-5(2H)-imines 4 react with N-(2,2,2-trichloroethylidene)-substituted amides 5 to form [3 + 2]-cycloaddition products 6 featured by an extra coordination of the ring sulfur atom to the terminal nitrogen atom of the side 1,3-diazapropenylide

ACYLATION OF 5-AMINO-2-ARYL-3-PHENYL-1,2,4-THIADIAZOLIUM CHLORIDES

Zyabrev, V.S.,Kharchenko, A.V.,Pirozhenko, V.V.,Drach, B.S.

, p. 1583 - 1590 (2007/10/02)

The chlornation of 1-(N-arylbenzimidoyl)thioureas under mild conditions leads to the formation of 5-amino-2-aryl-3-phenyl-1,2,4-thiadiazoluim chlorides, which are acylated at the exocyclic nitrogen atom when heated with carboxylic acid anhydrides or chlor

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