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diethyl 2-(isopropoxy(phenyl)methyl)malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1246669-01-1 Structure
  • Basic information

    1. Product Name: diethyl 2-(isopropoxy(phenyl)methyl)malonate
    2. Synonyms: diethyl 2-(isopropoxy(phenyl)methyl)malonate
    3. CAS NO:1246669-01-1
    4. Molecular Formula:
    5. Molecular Weight: 308.375
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1246669-01-1.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: diethyl 2-(isopropoxy(phenyl)methyl)malonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl 2-(isopropoxy(phenyl)methyl)malonate(1246669-01-1)
    11. EPA Substance Registry System: diethyl 2-(isopropoxy(phenyl)methyl)malonate(1246669-01-1)
  • 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: 1246669-01-1(Hazardous Substances Data)

1246669-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1246669-01-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,6,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1246669-01:
(9*1)+(8*2)+(7*4)+(6*6)+(5*6)+(4*6)+(3*9)+(2*0)+(1*1)=171
171 % 10 = 1
So 1246669-01-1 is a valid CAS Registry Number.

1246669-01-1Downstream Products

1246669-01-1Relevant articles and documents

Dehydrogenative functionalization of C(sp3)-H bonds adjacent to a heteroatom mediated by oxoammonium salts

Richter, Heinrich,Mancheno, Olga Garcia

experimental part, p. 4460 - 4467 (2010/10/04)

The first oxoammonium salt mediated formation of C-C bonds from, benzylic C(sp3)-H bonds adjacent to an oxygen or nitrogen, atom by dehydrogenative coupling with enolizable carbonyls has been developed. The use of these oxi- dants in combination with catalytic amounts of Fe(OTf)2 as Lewis acid, allows the reaction to be carried out under mild conditions, leading to the corresponding coupling products in moderate to good yields.

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