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2,2-dimethyl-propionic acid 1H-indol-2-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 426264-81-5 Structure
  • Basic information

    1. Product Name: 2,2-dimethyl-propionic acid 1H-indol-2-yl ester
    2. Synonyms: 2,2-dimethyl-propionic acid 1H-indol-2-yl ester
    3. CAS NO:426264-81-5
    4. Molecular Formula: C13H15NO2
    5. Molecular Weight: 217
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 426264-81-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2-dimethyl-propionic acid 1H-indol-2-yl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-dimethyl-propionic acid 1H-indol-2-yl ester(426264-81-5)
    11. EPA Substance Registry System: 2,2-dimethyl-propionic acid 1H-indol-2-yl ester(426264-81-5)
  • 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: 426264-81-5(Hazardous Substances Data)

426264-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 426264-81-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,6,2,6 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 426264-81:
(8*4)+(7*2)+(6*6)+(5*2)+(4*6)+(3*4)+(2*8)+(1*1)=145
145 % 10 = 5
So 426264-81-5 is a valid CAS Registry Number.

426264-81-5Downstream Products

426264-81-5Relevant articles and documents

N-Acylation of amides with acid anhydrides by way of dual activation using MgBr2·OEt2

Yamada, Shinji,Yaguchi, Setsuko,Matsuda, Kaori

, p. 647 - 651 (2002)

A new practical method for the N-acylation of amides is described. Acylation of various amides with acid anhydrides in the presence of MgBr2·OEt2 gave the corresponding N-acylamides in good to moderate yields. The present method is a

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