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83487-74-5

neophyl 3,7-bis(propargyloxy)-2-naphthoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83487-74-5 Structure

  • Basic information

    1. Product Name: neophyl 3,7-bis(propargyloxy)-2-naphthoate
    2. Synonyms: neophyl 3,7-bis(propargyloxy)-2-naphthoate
    3. CAS NO:83487-74-5
    4. Molecular Formula:
    5. Molecular Weight: 412.485
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83487-74-5.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: neophyl 3,7-bis(propargyloxy)-2-naphthoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: neophyl 3,7-bis(propargyloxy)-2-naphthoate(83487-74-5)
    11. EPA Substance Registry System: neophyl 3,7-bis(propargyloxy)-2-naphthoate(83487-74-5)

  • 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: 83487-74-5(Hazardous Substances Data)

83487-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83487-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,8 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83487-74:
(7*8)+(6*3)+(5*4)+(4*8)+(3*7)+(2*7)+(1*4)=165
165 % 10 = 5
So 83487-74-5 is a valid CAS Registry Number.

83487-74-5Downstream Products

83487-74-5Relevant articles and documents

1,8,17,24-Tetraoxa(2,6)naphthalenophane-3,5,19,21-tetrayne-10,13-dicarboxylic Acid Derivatives, Novel Complexors of Aromatic Guests

Jarvi, Esa T.,Whitlock, Howard W.

, p. 7196 - 7204 (2007/10/02)

Synthesis and complexation behavior of the title molecules are described.Study of aromatic solvent induced shifts of these molecules support the contention that their large cavity can accomodate aromatic rings.The behavior of acid 1a in water suggests that this effect enhanced in aqueous medium, as is expected for formation of hydrophobic inclusion complexes.In contrast to the rigid naphthalenophanes (1), their saturated derivatives (7) exist in a collapsed conformation and do not incorporate aromatic guests.

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