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123228-79-5

acrolein hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123228-79-5 Structure

  • Basic information

    1. Product Name: acrolein hydrazone
    2. Synonyms: acrolein hydrazone
    3. CAS NO:123228-79-5
    4. Molecular Formula:
    5. Molecular Weight: 70.094
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123228-79-5.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: acrolein hydrazone(CAS DataBase Reference)
    10. NIST Chemistry Reference: acrolein hydrazone(123228-79-5)
    11. EPA Substance Registry System: acrolein hydrazone(123228-79-5)

  • 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: 123228-79-5(Hazardous Substances Data)

123228-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123228-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,2 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 123228-79:
(8*1)+(7*2)+(6*3)+(5*2)+(4*2)+(3*8)+(2*7)+(1*9)=105
105 % 10 = 5
So 123228-79-5 is a valid CAS Registry Number.

123228-79-5Upstream product

123228-79-5Downstream Products

123228-79-5Relevant articles and documents

Photochemistry of Azocyclopropane

Engel, Paul S.,Bodager, Gregory A.

, p. 4748 - 4758 (1988)

trans-Azocyclopropane (1t) has been irradiated in the gas phase at 254 nm and in hydrocarbon solution at several wavelengths.As with most acyclic azoalkanes, the dominant reaction is isomarization to the cis-azoalkane 1c.In the gas phase or with short wavelength light, 1t undergoes competitive C-N homolysis, giving cyclopropyl radicals, and ring fragmentation to ethylene.Triplet-sensitized isomerization of the azo linkage proceeds with unusually high efficiency (Φt->c=0.2), but no experimental support could be found for the notion that cyclopropane ring cleavage leads to azo group isomerization.Since azocyclopropane behaves as a "reluctant azoalkane" that undergoes multiple photoreactions, it is not a particularly useful source of cyclopropyl radicals.

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