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(+)-threo-1,5-diphenylpentane-1,3-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 61952-19-0 Structure
  • Basic information

    1. Product Name: (+)-threo-1,5-diphenylpentane-1,3-diol
    2. Synonyms:
    3. CAS NO:61952-19-0
    4. Molecular Formula:
    5. Molecular Weight: 256.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 61952-19-0.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: (+)-threo-1,5-diphenylpentane-1,3-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-threo-1,5-diphenylpentane-1,3-diol(61952-19-0)
    11. EPA Substance Registry System: (+)-threo-1,5-diphenylpentane-1,3-diol(61952-19-0)
  • 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: 61952-19-0(Hazardous Substances Data)

61952-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61952-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,5 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61952-19:
(7*6)+(6*1)+(5*9)+(4*5)+(3*2)+(2*1)+(1*9)=130
130 % 10 = 0
So 61952-19-0 is a valid CAS Registry Number.

61952-19-0Downstream Products

61952-19-0Relevant articles and documents

Double Catalytic Kinetic Resolution (DoCKR) of Acyclic anti-1,3-Diols: The Additive Horeau Amplification

Merad, Jérémy,Borkar, Prashant,Caijo, Frédéric,Pons, Jean-Marc,Parrain, Jean-Luc,Chuzel, Olivier,Bressy, Cyril

, p. 16052 - 16056 (2017)

The concept of a synergistic double catalytic kinetic resolution (DoCKR) as described in this article was successfully applied to racemic acyclic anti-1,3-diols, a common motif in natural products. This process takes advantage of an additive Horeau amplif

HETEROATOM DIRECTED Β-LITHIATION OF A VINYL ETHER

McDougal, Patrick G.,Rico, Joseph G.

, p. 5977 - 5980 (2007/10/02)

Oxygen directed β-deprotonation of a vinyl ether leads to Z substituted enol ethers.The stereoselective elaboration to a naturally occuring threo 1,3-diol is described.

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