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152035-54-6

2-<2-<3-(Tosyloxy)propoxy>phenyl>-1,3-dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 152035-54-6 Structure

  • Basic information

    1. Product Name: 2-<2-<3-(Tosyloxy)propoxy>phenyl>-1,3-dioxolane
    2. Synonyms: 2-<2-<3-(Tosyloxy)propoxy>phenyl>-1,3-dioxolane
    3. CAS NO:152035-54-6
    4. Molecular Formula:
    5. Molecular Weight: 378.446
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 152035-54-6.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-<3-(Tosyloxy)propoxy>phenyl>-1,3-dioxolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-<2-<3-(Tosyloxy)propoxy>phenyl>-1,3-dioxolane(152035-54-6)
    11. EPA Substance Registry System: 2-<2-<3-(Tosyloxy)propoxy>phenyl>-1,3-dioxolane(152035-54-6)

  • 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: 152035-54-6(Hazardous Substances Data)

152035-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152035-54-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,0,3 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 152035-54:
(8*1)+(7*5)+(6*2)+(5*0)+(4*3)+(3*5)+(2*5)+(1*4)=96
96 % 10 = 6
So 152035-54-6 is a valid CAS Registry Number.

152035-54-6Relevant articles and documents

Synthesis of New Five-Atom-Linked Capped Porphyrins

Ma, Wuping,Slebodnick, Carla,Ibers, James A.

, p. 6349 - 6353 (2007/10/02)

The synthesis and characterization of three new five-atom-linked "capped" porphyrins, 6, 12, and 18, are reported.The general synthetic procedure involves synthesis of a tetraaldehyde "cap" by reacting the five-atom "arm" with 1,2,4,5-tetrahydroxybenzene

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