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2-Hexenoic acid, 5-methyl-4-(phenylseleno)-, ethyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 154870-06-1 Structure
  • Basic information

    1. Product Name: 2-Hexenoic acid, 5-methyl-4-(phenylseleno)-, ethyl ester, (E)-
    2. Synonyms:
    3. CAS NO:154870-06-1
    4. Molecular Formula: C15H20O2Se
    5. Molecular Weight: 311.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154870-06-1.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-Hexenoic acid, 5-methyl-4-(phenylseleno)-, ethyl ester, (E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Hexenoic acid, 5-methyl-4-(phenylseleno)-, ethyl ester, (E)-(154870-06-1)
    11. EPA Substance Registry System: 2-Hexenoic acid, 5-methyl-4-(phenylseleno)-, ethyl ester, (E)-(154870-06-1)
  • 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: 154870-06-1(Hazardous Substances Data)

154870-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154870-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,8,7 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 154870-06:
(8*1)+(7*5)+(6*4)+(5*8)+(4*7)+(3*0)+(2*0)+(1*6)=141
141 % 10 = 1
So 154870-06-1 is a valid CAS Registry Number.

154870-06-1Downstream Products

154870-06-1Relevant articles and documents

Synthesis of α-halo β,γ-unsaturated esters from γ-phenylseleno α,β-unsaturated esters

Duclos, Jean-Francois,Outurquin, Francis,Paulmier, Claude

, p. 7417 - 7420 (1993)

γ-Phenylseleno α,β-unsaturated esters, prepared from α-phenylseleno aldehydes by Horner-Emmons reaction and treated with bromine or sulfuryl chloride, form adducts whose decomposition leads to α-halo β,γ-unsaturated esters in fair to good yields.

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