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CAS

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127527-03-1

2-(2-methoxy-5-nitro-phenyl)-pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127527-03-1 Structure

  • Basic information

    1. Product Name: 2-(2-methoxy-5-nitro-phenyl)-pyridine
    2. Synonyms:
    3. CAS NO:127527-03-1
    4. Molecular Formula:
    5. Molecular Weight: 230.223
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127527-03-1.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-(2-methoxy-5-nitro-phenyl)-pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-methoxy-5-nitro-phenyl)-pyridine(127527-03-1)
    11. EPA Substance Registry System: 2-(2-methoxy-5-nitro-phenyl)-pyridine(127527-03-1)

  • 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: 127527-03-1(Hazardous Substances Data)

127527-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127527-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,2 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127527-03:
(8*1)+(7*2)+(6*7)+(5*5)+(4*2)+(3*7)+(2*0)+(1*3)=121
121 % 10 = 1
So 127527-03-1 is a valid CAS Registry Number.

127527-03-1Relevant articles and documents

TAUTOMERS OF AZINE DERIVATIVES. 21. TAUTOMERISM IN 2-(2-HYDROXYARYL)AZINES

Stekhova, S. A.,Lapachev, V. V.,Mamaev, V. P.

, p. 65 - 70 (2007/10/02)

Tautomerism in 2-(2-hydroxyaryl)azines has been studied using 17O NMR and UV spectroscopy.Consideration has been given to the influence of solvent and structural factors which facilitate the establishment of a tautomeric equilibrium in these compounds.

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