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55075-33-7

1-Ethoxy-1-phenyl-1-(2-hydroxy-naphthyl)-methan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55075-33-7 Structure

  • Basic information

    1. Product Name: 1-Ethoxy-1-phenyl-1-(2-hydroxy-naphthyl)-methan
    2. Synonyms: 1-Ethoxy-1-phenyl-1-(2-hydroxy-naphthyl)-methan
    3. CAS NO:55075-33-7
    4. Molecular Formula:
    5. Molecular Weight: 278.351
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55075-33-7.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: 1-Ethoxy-1-phenyl-1-(2-hydroxy-naphthyl)-methan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Ethoxy-1-phenyl-1-(2-hydroxy-naphthyl)-methan(55075-33-7)
    11. EPA Substance Registry System: 1-Ethoxy-1-phenyl-1-(2-hydroxy-naphthyl)-methan(55075-33-7)

  • 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: 55075-33-7(Hazardous Substances Data)

55075-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55075-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,7 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55075-33:
(7*5)+(6*5)+(5*0)+(4*7)+(3*5)+(2*3)+(1*3)=117
117 % 10 = 7
So 55075-33-7 is a valid CAS Registry Number.

55075-33-7Downstream Products

55075-33-7Relevant articles and documents

A direct approach for the expedient synthesis of unsymmetrical ethers by employing bromodimethylsulfonium bromide (BDMS) mediated C-S bond cleavage of naphthalene-2-ol sulfides

Islam, Kobirul,Sidick Basha,Dar, Ajaz A.,Das, Deb K.,Khan, Abu T.

, p. 79759 - 79764 (2015)

The unsymmetrical ether derivatives 1-(alkoxy(aryl)methyl)naphthalen-2-ols (3a-q) were synthesized from 1-(aryl(alkyl/arylthio)methyl)-naphthalene-2-ol derivatives (1) and alcohols (2) by cleavage of C-S bond using bromodimethylsulfonium bromide (BDMS) at

Mannich Bases, XXI: Exchange Reactions of Phenolic Mannich Bases

Moehrle, Hans,Miller, Christoph

, p. 229 - 236 (2007/10/02)

Various p-substituted phenolic Mannich bases (and to a minor degree o-substituted derivatives) form alcohols and ethers when heated in aqueous alcohols in the presence of Na2EDTA or acetic acid.The reaction proceeds with amine elimination and subsequent addition of the solvent to the resulting quinone methide.

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