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CAS

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55696-63-4

anti-1,5-diphenyl-1,5-propanediol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55696-63-4 Structure

  • Basic information

    1. Product Name: anti-1,5-diphenyl-1,5-propanediol
    2. Synonyms:
    3. CAS NO:55696-63-4
    4. Molecular Formula:
    5. Molecular Weight: 256.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55696-63-4.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: anti-1,5-diphenyl-1,5-propanediol(CAS DataBase Reference)
    10. NIST Chemistry Reference: anti-1,5-diphenyl-1,5-propanediol(55696-63-4)
    11. EPA Substance Registry System: anti-1,5-diphenyl-1,5-propanediol(55696-63-4)

  • 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: 55696-63-4(Hazardous Substances Data)

55696-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55696-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,9 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55696-63:
(7*5)+(6*5)+(5*6)+(4*9)+(3*6)+(2*6)+(1*3)=164
164 % 10 = 4
So 55696-63-4 is a valid CAS Registry Number.

55696-63-4Downstream Products

55696-63-4Relevant articles and documents

Facile reduction of aromatic aldehydes, ketones, diketones and oxo aldehydes to alcohols by an aqueous TiCl3/NH3 system: Selectivity and scope

Clerici, Angelo,Pastori, Nadia,Porta, Ombretta

, p. 3326 - 3335 (2002)

A simple and rapid procedure for the almost quantitative reduction of aromatic aldehydes, ketones, diketones and oxo aldehydes to alcohols by use of TiCl3/NH3 in aqueous methanol solution is reported. The reducing system distinguishes between different classes of aldehydes and/or ketones, and many functionalities that usually do not survive under reducing conditions are tolerated well. The concept of reversal of chemoselectivity has also been developed. A mechanism based on two sequential one-electron transfers from TiIII to the carbonyl carbon atom is proposed, the second SET becoming operative only in the presence of ammonium ion (either added or formed in situ). Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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