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127680-05-1

((E)-Hept-1-enyl)-phenyl-diazene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127680-05-1 Structure

  • Basic information

    1. Product Name: ((E)-Hept-1-enyl)-phenyl-diazene
    2. Synonyms:
    3. CAS NO:127680-05-1
    4. Molecular Formula:
    5. Molecular Weight: 202.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127680-05-1.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: ((E)-Hept-1-enyl)-phenyl-diazene(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((E)-Hept-1-enyl)-phenyl-diazene(127680-05-1)
    11. EPA Substance Registry System: ((E)-Hept-1-enyl)-phenyl-diazene(127680-05-1)

  • 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: 127680-05-1(Hazardous Substances Data)

127680-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127680-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,8 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127680-05:
(8*1)+(7*2)+(6*7)+(5*6)+(4*8)+(3*0)+(2*0)+(1*5)=131
131 % 10 = 1
So 127680-05-1 is a valid CAS Registry Number.

127680-05-1Relevant articles and documents

1-PHENYLAZO-1-ALKENES

Schantl, Joachim G.,Hebeisen, Paul

, p. 395 - 406 (2007/10/02)

Aliphatic aldehyde phenylhydrazones 1 were converted into 1-phenylazo-1-alkenes 3 either by the reaction with I2 and pyridine followed by base induced 1,4-elimination of pyridine.HI (Method A), or via N-(4-methylbenzenesulfonyl)-N-phenylhydrazones 7 which undergo 1,4-elimination of p-toluenesulfinic acid upon treatment with KOt-Bu (Method B).Both procedures yield mixtures of configurational isomers of the phenylazo-alkenes EE- and EZ- 3b-3e; Method B is giving rise to the kinetically controlled isomer mixture (EZ-3 predominant), which equilibrates to the thremodynamicratio (EE-3 predominant) as afforded by Method A.

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