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36178-06-0

5,8-dihydro-5,8-epoxyquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 36178-06-0 Structure

  • Basic information

    1. Product Name: 5,8-dihydro-5,8-epoxyquinoline
    2. Synonyms: 5,8-dihydro-5,8-epoxyquinoline
    3. CAS NO:36178-06-0
    4. Molecular Formula:
    5. Molecular Weight: 145.161
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 36178-06-0.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: 5,8-dihydro-5,8-epoxyquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,8-dihydro-5,8-epoxyquinoline(36178-06-0)
    11. EPA Substance Registry System: 5,8-dihydro-5,8-epoxyquinoline(36178-06-0)

  • 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: 36178-06-0(Hazardous Substances Data)

36178-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36178-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,7 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36178-06:
(7*3)+(6*6)+(5*1)+(4*7)+(3*8)+(2*0)+(1*6)=120
120 % 10 = 0
So 36178-06-0 is a valid CAS Registry Number.

36178-06-0Relevant articles and documents

2,3-Pyridyne formation by fluoride induced desilylation-elimination

Walters, Michael A.,Shay, John J.

, p. 3573 - 3579 (1997)

The formation of 2,3-pyridyne by a desilylation-elimination sequence employing anhydrous CsF is reported.

Rh(I)-catalyzed ring-opening of hetaryne-furan diels-alder adducts: Rapid access to stereochemically defined heterocyclic scaffolds

Nguyen, Trung D.,Webster, Robert,Lautens, Mark

supporting information; experimental part, p. 1370 - 1373 (2011/05/15)

Probing the nucleophilic ring-opening of various bicyclic [2.2.1] hetaryne-furan Diels-Alder adducts revealed that efficient reactivity could be observed with heteroatom nucleophiles by using a cationic Rh(I) complex in combination with a chiral Josiphos-

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