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1202914-02-0

C20H15ClN2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1202914-02-0 Structure

  • Basic information

    1. Product Name: C20H15ClN2
    2. Synonyms:
    3. CAS NO:1202914-02-0
    4. Molecular Formula:
    5. Molecular Weight: 318.805
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1202914-02-0.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: C20H15ClN2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H15ClN2(1202914-02-0)
    11. EPA Substance Registry System: C20H15ClN2(1202914-02-0)

  • 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: 1202914-02-0(Hazardous Substances Data)

1202914-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1202914-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,9,1 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1202914-02:
(9*1)+(8*2)+(7*0)+(6*2)+(5*9)+(4*1)+(3*4)+(2*0)+(1*2)=100
100 % 10 = 0
So 1202914-02-0 is a valid CAS Registry Number.

1202914-02-0Downstream Products

1202914-02-0Relevant articles and documents

Solvent-free three component Strecker reaction of ketones using highly recyclable and hydrophobic sulfonic acid based nanoreactors

Karimi, Babak,Zareyee, Daryoush

, p. 8665 - 8670 (2009)

An efficient and environmentally benign system was developed for the one-pot three-component Strecker reaction of ketones under solvent-free conditions, with the use of a highly recoverable SBA-15 supported sulfonic acid. Also findings concerning the effects of functionalized inert groups and silica backbone pore size on substrate scope, catalytic activity and recycling behavior of the catalysts were briefly discussed. The simple experimental and product isolation procedure accompanied by easy recovery and reusability of the catalyst could be considered as attractive features of this new protocol which will hopefully develop a clean strategy for the synthesis of α-amino nitriles. The Royal Society of Chemistry 2009.

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