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CAS

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180057-12-9

6-Chloro-9-o-tolyl-thieno[2,3-c][1,5]naphthyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 180057-12-9 Structure

  • Basic information

    1. Product Name: 6-Chloro-9-o-tolyl-thieno[2,3-c][1,5]naphthyridine
    2. Synonyms: 6-Chloro-9-o-tolyl-thieno[2,3-c][1,5]naphthyridine
    3. CAS NO:180057-12-9
    4. Molecular Formula:
    5. Molecular Weight: 310.807
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 180057-12-9.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: 6-Chloro-9-o-tolyl-thieno[2,3-c][1,5]naphthyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Chloro-9-o-tolyl-thieno[2,3-c][1,5]naphthyridine(180057-12-9)
    11. EPA Substance Registry System: 6-Chloro-9-o-tolyl-thieno[2,3-c][1,5]naphthyridine(180057-12-9)

  • 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: 180057-12-9(Hazardous Substances Data)

180057-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180057-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,0,5 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 180057-12:
(8*1)+(7*8)+(6*0)+(5*0)+(4*5)+(3*7)+(2*1)+(1*2)=109
109 % 10 = 9
So 180057-12-9 is a valid CAS Registry Number.

180057-12-9Downstream Products

180057-12-9Relevant articles and documents

4-Substituted 1-(2-methylphenyl)thieno[2,3-c]-1,5-naphthyridines as possible reversible inhibitors of gastric M+,K+-ATPase

Bjork,Hornfeldt,Gronowitz,Edvardsson

, p. 411 - 416 (2007/10/03)

Seven 1-(2-methylphenyl)thieno[2,3-c]-1,5-naphthyridines substituted in the 4-position with different amino-containing groups have been prepared. The reaction route to these compounds consisted of a palladium(0)-catalyzed cross-coupling between 1-bromothieno[2,3-c]-1,5-naphthyridine and 2-methyl-1-trimethylstannylbenzene, then oxidation of the 5-nitrogen, followed by treatment with thionyl chloride to give the 4-chloro derivative. The compounds obtained after nucleophilic substitution were tested with regard to their effects on H+,K+-ATPase activity and on acid formation in gastric glands. However, the inhibitory potency in vitro of the substituted naphthyridines was not high enough to be of interest from a pharmacological point of view.

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