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CAS

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1333235-01-0

C17H16Cl2O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1333235-01-0 Structure

  • Basic information

    1. Product Name: C17H16Cl2O3
    2. Synonyms: C17H16Cl2O3
    3. CAS NO:1333235-01-0
    4. Molecular Formula:
    5. Molecular Weight: 339.218
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1333235-01-0.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: C17H16Cl2O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H16Cl2O3(1333235-01-0)
    11. EPA Substance Registry System: C17H16Cl2O3(1333235-01-0)

  • 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: 1333235-01-0(Hazardous Substances Data)

1333235-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333235-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,2,3 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1333235-01:
(9*1)+(8*3)+(7*3)+(6*3)+(5*2)+(4*3)+(3*5)+(2*0)+(1*1)=110
110 % 10 = 0
So 1333235-01-0 is a valid CAS Registry Number.

1333235-01-0Downstream Products

1333235-01-0Relevant articles and documents

Asymmetric organocatalytic aldol reaction in water: Mechanistic insights and development of a semi-continuously operating process

Rulli, Giuseppe,Fredriksen, Kim A.,Duangdee, Nongnaphat,Bonge-Hansen, Tore,Berkessel, Albrecht,Groeger, Harald

, p. 2512 - 2519 (2013)

A detailed study on the impact of the catalyst loading on conversion and enantioselectivity of the direct aldol reaction of an aldehyde and acetone in aqueous solvent with nonimmobilized and immobilized proline amide-based organocatalysts is described. Based on a polymer-supported catalyst, batch and semi-continuously operating processes, comprising recycling studies in the latter case, were investigated.

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