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126963-72-2

Benzyl-[tetrahydro-pyran-(2Z)-ylidene]-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126963-72-2 Structure

  • Basic information

    1. Product Name: Benzyl-[tetrahydro-pyran-(2Z)-ylidene]-amine
    2. Synonyms: Benzyl-[tetrahydro-pyran-(2Z)-ylidene]-amine
    3. CAS NO:126963-72-2
    4. Molecular Formula:
    5. Molecular Weight: 189.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126963-72-2.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: Benzyl-[tetrahydro-pyran-(2Z)-ylidene]-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzyl-[tetrahydro-pyran-(2Z)-ylidene]-amine(126963-72-2)
    11. EPA Substance Registry System: Benzyl-[tetrahydro-pyran-(2Z)-ylidene]-amine(126963-72-2)

  • 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: 126963-72-2(Hazardous Substances Data)

126963-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126963-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,6 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126963-72:
(8*1)+(7*2)+(6*6)+(5*9)+(4*6)+(3*3)+(2*7)+(1*2)=152
152 % 10 = 2
So 126963-72-2 is a valid CAS Registry Number.

126963-72-2Downstream Products

126963-72-2Relevant articles and documents

Facile preparation of 2-imino tetrahydrofurans, pyrans and oxepans

Alanine,Fishwick,Szantay Jr.

, p. 6571 - 6572 (2007/10/02)

A simple and convenient route to 2-imino tetrahydrofurans, pyrans and oxepans which utilizes a silver-assisted intramolecular O-alkylation has been developed and produces these novel imidates in good yields and with high stereoselectivity.

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