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182319-50-2

2-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-tetrahydro-pyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 182319-50-2 Structure

  • Basic information

    1. Product Name: 2-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-tetrahydro-pyran
    2. Synonyms: 2-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-tetrahydro-pyran
    3. CAS NO:182319-50-2
    4. Molecular Formula:
    5. Molecular Weight: 374.072
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 182319-50-2.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-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-tetrahydro-pyran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-tetrahydro-pyran(182319-50-2)
    11. EPA Substance Registry System: 2-[3-(3,5-Dibromo-phenyl)-prop-2-ynyloxy]-tetrahydro-pyran(182319-50-2)

  • 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: 182319-50-2(Hazardous Substances Data)

182319-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182319-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,3,1 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 182319-50:
(8*1)+(7*8)+(6*2)+(5*3)+(4*1)+(3*9)+(2*5)+(1*0)=132
132 % 10 = 2
So 182319-50-2 is a valid CAS Registry Number.

182319-50-2Relevant articles and documents

Multiply bridged acetylenic thiacyclophanes

Ensley, Harry E.,Mahadevan, Shivkumar,Mague, Joel

, p. 6255 - 6258 (1996)

The 4,17,30-trithia-[73](1,3,5)cyclophane (1) has been prepared by a two-stage, palladium assisted coupling of propargylOTHP with 1,3,5-tribromobenzene, followed by sulfide ring closure. The intermediate (8) on deprotection, followed by bromination and reaction with Na2S gives 1 in 58% yield.

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