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652150-92-0

2-Oxetanone,3-ethyl-4-[(phenylmethoxy)methyl]-,(3R,4R)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 652150-92-0 Structure

  • Basic information

    1. Product Name: 2-Oxetanone,3-ethyl-4-[(phenylmethoxy)methyl]-,(3R,4R)-(9CI)
    2. Synonyms: 2-Oxetanone,3-ethyl-4-[(phenylmethoxy)methyl]-,(3R,4R)-(9CI)
    3. CAS NO:652150-92-0
    4. Molecular Formula: C13H16O3
    5. Molecular Weight: 220.26
    6. EINECS: N/A
    7. Product Categories: ETHYL
    8. Mol File: 652150-92-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Oxetanone,3-ethyl-4-[(phenylmethoxy)methyl]-,(3R,4R)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Oxetanone,3-ethyl-4-[(phenylmethoxy)methyl]-,(3R,4R)-(9CI)(652150-92-0)
    11. EPA Substance Registry System: 2-Oxetanone,3-ethyl-4-[(phenylmethoxy)methyl]-,(3R,4R)-(9CI)(652150-92-0)

  • 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: 652150-92-0(Hazardous Substances Data)

652150-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 652150-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,2,1,5 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 652150-92:
(8*6)+(7*5)+(6*2)+(5*1)+(4*5)+(3*0)+(2*9)+(1*2)=140
140 % 10 = 0
So 652150-92-0 is a valid CAS Registry Number.

652150-92-0Downstream Products

652150-92-0Relevant articles and documents

Catalytic Asymmetric Acyl Halide-Aldehyde Cyclocondensation Reactions of Substituted Ketenes

Nelson, Scott G.,Zhu, Cheng,Shen, Xiaoqiang

, p. 14 - 15 (2007/10/03)

Catalytic asymmetric acyl halide-aldehyde cyclocondensation (AAC) reactions of alkyl-substituted ketenes with structurally diverse aldehydes provide cis-disubstituted β-lactones with high enantioselectivity. The AAC reactions utilize a novel Al(III)-triamine catalyst in which the metal′s dynamic coordination geometry leads to a highly selective catalyst complex. These AAC reactions represent a functional solution to highly enantioselective substituted ester enolate aldol additions. Copyright

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