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N1-(4-chlorophenyl)-4-chloro-1-benzenecarboximidamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138240-23-0

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138240-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138240-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,2,4 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138240-23:
(8*1)+(7*3)+(6*8)+(5*2)+(4*4)+(3*0)+(2*2)+(1*3)=110
110 % 10 = 0
So 138240-23-0 is a valid CAS Registry Number.

138240-23-0Relevant academic research and scientific papers

Facile Synthesis of Amidines via the Intermolecular Reductive Coupling of Nitriles with Nitro Compounds Induced by Samarium(II) Iodide

Zhou, Longhu,Zhang, Yongmin

, p. 596 - 597 (1998)

The intermolecular reductive coupling of nitriles with nitro compounds induced by Sml2 was studied; amidine derivatives are prepared in good yields under neutral and mild conditions.

Low-valent titanium induced reductive coupling of nitriles with nitro compounds

Zhou, Longhu,Zhang, Yongmin

, p. 3249 - 3262 (1998)

The intermolecular and intramolecular reductive coupling of a cyano group with a nitro group induced by a low-valent titanium reagent prepared from TiCl4/Sm was studied. Amidines and 2-aminoquinolines derivatives are prepared in good yields under mild conditions respectively.

Samarium(II) iodide induced reductive coupling of nitriles with nitro compounds

Zhou, Longhu,Zhang, Yongmin

, p. 2899 - 2902 (1998)

The intermolecular and intramolecular reductive coupling of a cyano group with a nitro group induced by SmI2 was studied. Amidines and 2-aminoquinoline derivatives are prepared in good yields under neutral and mild conditions respectively.

Synthesis, structure-activity relationships at the GABAA receptor in rat brain, and differential electrophysiological profile at the recombinant human GABAA receptor of a series of substituted 1,2-diphenylimidazoles

Asproni, Battistina,Talani, Giuseppe,Busonero, Fabio,Pau, Amedeo,Sanna, Sebastiano,Cerri, Riccardo,Mascia, Maria Paola,Sanna, Enrico,Biggio, Giovanni

, p. 2638 - 2645 (2007/10/03)

A series of new 1,2-diphenylimidazole derivatives (1a-x) were synthesized and evaluated for their ability to potentiate γ-aminobutyric acid (GABA)-evoked currents in Xenopus laevis oocytes expressing recombinant human GABAA receptors. Many of t

Reactions of Aryliminodimagnesium with Some N,N-Dimethylcarboxamides and Benzonitriles Affording Various Types of Amidines. Correction of Previous Results on Formamidine Formation from N,N-Dimethylformamide

Okubo, Masao,Tanaka, Mikio,Murata, Yuri,Tsurusaki, Nobuyuki,Omote, Yasumasa,et al.

, p. 1965 - 1968 (2007/10/02)

Some symmetrical and unsymmetrical form- and benzamidines were prepared by the reaction of ArN(MgBr)2 with Ar'CN, HCONMe2 and related compounds in tetrahydrofuran.

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