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1018553-10-0

C11H12N2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1018553-10-0 Structure

  • Basic information

    1. Product Name: C11H12N2
    2. Synonyms:
    3. CAS NO:1018553-10-0
    4. Molecular Formula:
    5. Molecular Weight: 172.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1018553-10-0.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: C11H12N2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H12N2(1018553-10-0)
    11. EPA Substance Registry System: C11H12N2(1018553-10-0)

  • 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: 1018553-10-0(Hazardous Substances Data)

1018553-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1018553-10-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,5,5 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1018553-10:
(9*1)+(8*0)+(7*1)+(6*8)+(5*5)+(4*5)+(3*3)+(2*1)+(1*0)=120
120 % 10 = 0
So 1018553-10-0 is a valid CAS Registry Number.

1018553-10-0Relevant articles and documents

Synthesis of iminonitriles by oxone/tbab-mediated one-pot oxidative three-component strecker reaction

Gualtierotti, Jean-Baptiste,Schumacher, Xavier,Wang, Qian,Zhu, Jieping

, p. 1380 - 1386 (2013)

Oxidative three-component reaction of aldehydes, amines, and TMSCN in a biphasic solvent system (toluene/H2O) containing Oxone, tetra-n-butylammonium bromide (TBAB) and sodium bicarbonate afforded α-iminonitriles in good to excellent yields. This oxidative Strecker reaction was applicable to a wide range of aldehydes and amines, aromatic or aliphatic, of different electronic and steric properties. Substituted 1-aza-2-cyano-1,3-dienes were also accessible using α,β-unsaturated aldehydes as inputs.

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