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1-(2-Nitro-phenyl)-pentadien-1,3-saeure-5-methylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72232-02-1 Structure
  • Basic information

    1. Product Name: 1-(2-Nitro-phenyl)-pentadien-1,3-saeure-5-methylester
    2. Synonyms:
    3. CAS NO:72232-02-1
    4. Molecular Formula:
    5. Molecular Weight: 233.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72232-02-1.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: 1-(2-Nitro-phenyl)-pentadien-1,3-saeure-5-methylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-Nitro-phenyl)-pentadien-1,3-saeure-5-methylester(72232-02-1)
    11. EPA Substance Registry System: 1-(2-Nitro-phenyl)-pentadien-1,3-saeure-5-methylester(72232-02-1)
  • 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: 72232-02-1(Hazardous Substances Data)

72232-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72232-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,3 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72232-02:
(7*7)+(6*2)+(5*2)+(4*3)+(3*2)+(2*0)+(1*2)=91
91 % 10 = 1
So 72232-02-1 is a valid CAS Registry Number.

72232-02-1Downstream Products

72232-02-1Relevant articles and documents

Tandem oxidation-Wittig-Wittig sequences for the preparation of functionalised dienoates

Lang, Stuart,Taylor, Richard J.K.

, p. 5489 - 5492 (2006)

A range of functionalised dienes and trienes have been prepared by one-pot processes in which alcohol oxidation is accompanied by in situ Wittig homologation using Trippett's reagent [(triphenylphosphoranylidene)acetaldehyde] followed by addition of a sec

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