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124619-05-2

(5-Methoxy-2-methoxymethyl-phenyl)-(4-methoxy-phenyl)-acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124619-05-2 Structure

  • Basic information

    1. Product Name: (5-Methoxy-2-methoxymethyl-phenyl)-(4-methoxy-phenyl)-acetonitrile
    2. Synonyms:
    3. CAS NO:124619-05-2
    4. Molecular Formula:
    5. Molecular Weight: 297.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124619-05-2.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: (5-Methoxy-2-methoxymethyl-phenyl)-(4-methoxy-phenyl)-acetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5-Methoxy-2-methoxymethyl-phenyl)-(4-methoxy-phenyl)-acetonitrile(124619-05-2)
    11. EPA Substance Registry System: (5-Methoxy-2-methoxymethyl-phenyl)-(4-methoxy-phenyl)-acetonitrile(124619-05-2)

  • 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: 124619-05-2(Hazardous Substances Data)

124619-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124619-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,6,1 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124619-05:
(8*1)+(7*2)+(6*4)+(5*6)+(4*1)+(3*9)+(2*0)+(1*5)=112
112 % 10 = 2
So 124619-05-2 is a valid CAS Registry Number.

124619-05-2Relevant articles and documents

Preparation of Novel 4-Substituted 6-Methoxy, 6,7-Dimethoxy-, and 6,7-(Methylenedioxy)isochroman-3-ones. 2

Khanapure, Subhash P.,Biehl, Edward R.

, p. 1471 - 1475 (2007/10/02)

The title compounds 20, 21, and 22 have been prepared in modest yields by a two-step reaction involving first the reaction of bromoarenes 3, 7, and 8 with lithioalkyl- and lithioarylacetonitriles under aryne-forming conditions.The cyano products 10, 14, and 16 so formed were then converted to the corresponding isochroman-3-ones by acidic hydrolysis.

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