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10-phenyl-6,7,8,9-terahydrobenzo<1,7>naphtyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125867-45-0

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  • 125867-45-0 Structure
  • Basic information

    1. Product Name: 10-phenyl-6,7,8,9-terahydrobenzo<1,7>naphtyridine
    2. Synonyms:
    3. CAS NO:125867-45-0
    4. Molecular Formula:
    5. Molecular Weight: 260.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125867-45-0.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: 10-phenyl-6,7,8,9-terahydrobenzo<1,7>naphtyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 10-phenyl-6,7,8,9-terahydrobenzo<1,7>naphtyridine(125867-45-0)
    11. EPA Substance Registry System: 10-phenyl-6,7,8,9-terahydrobenzo<1,7>naphtyridine(125867-45-0)
  • 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: 125867-45-0(Hazardous Substances Data)

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125867-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125867-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,6 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 125867-45:
(8*1)+(7*2)+(6*5)+(5*8)+(4*6)+(3*7)+(2*4)+(1*5)=150
150 % 10 = 0
So 125867-45-0 is a valid CAS Registry Number.

125867-45-0Downstream Products

125867-45-0Relevant articles and documents

Synthesis of ortho-substituted aminopyridines. Metalation of pivaloylamino derivatives

Estel,Linard,Marsais,Godard,Queguiner

, p. 105 - 112 (2007/10/02)

The three isomeric pivaloylaminopyridines were lithiated in more than 80% yields. Aminopyridine derivatives were treated by 2.5-3 equivalents of the complex BuLi-TMEDA at -10° in diethyl ether. Reaction of the lithiated species with various electrophiles afforded a number of ortho-substituted pivaloylaminopyridines in good yields. Secondary pyridine alcohols were oxidized to the corresponding aminopyridyl ketones. Pyridopyrimidines, benzonaphthyridines as well as an analogue of the natural antitumor alkaloid ellipticine has been synthesized showing the versatility of the method.

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