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106747-01-7

2-(5,6-Dimethoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-phenylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 106747-01-7 Structure

  • Basic information

    1. Product Name: 2-(5,6-Dimethoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-phenylamine
    2. Synonyms: 2-(5,6-Dimethoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-phenylamine
    3. CAS NO:106747-01-7
    4. Molecular Formula:
    5. Molecular Weight: 315.396
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 106747-01-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(5,6-Dimethoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-phenylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(5,6-Dimethoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-phenylamine(106747-01-7)
    11. EPA Substance Registry System: 2-(5,6-Dimethoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-phenylamine(106747-01-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 106747-01-7(Hazardous Substances Data)

106747-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106747-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,4 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106747-01:
(8*1)+(7*0)+(6*6)+(5*7)+(4*4)+(3*7)+(2*0)+(1*1)=117
117 % 10 = 7
So 106747-01-7 is a valid CAS Registry Number.

106747-01-7Relevant articles and documents

Substituted 2-anilines as Potential Inhibitors of H+/K+ ATPase

Adelstein, Gilbert W.,Yen, Chung H.,Haack, Richard A.,Yu, Stella,Gullikson, Gary,et al.

, p. 1215 - 1220 (2007/10/02)

A series of substituted 2-anilines were synthesized as potential inhibitors of the acid secretory enzyme H+/K+ ATPase.Substitutions on the aniline nitrogen atom resulted in potent enzyme inhibition in vitro but weak activity in gastric fistula dogs.Electron-donating substituents on the aniline ring enhanced in vitro and in vivo potency relative to the unubstituted analogue.The potency showed a correlation to the calculated pKa of the aniline nitrogen atom.Substitutions on the aniline and benzimidazole rings did not further enhance potency.Di- and trisubstituted aniline derivatives were potent inhibitors of the enzyme system.The preferred combination of substituents were a methoxy group on the benzimidazole ring and a single alkyl group on the aniline ring.One such compound, 76, was an effective inhibitor of acid secretion in the dog and was selected for further pharmacological study.

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