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bis(2,4,6-trichlorophenyl) allylmalonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1227926-43-3 Structure
  • Basic information

    1. Product Name: bis(2,4,6-trichlorophenyl) allylmalonate
    2. Synonyms: bis(2,4,6-trichlorophenyl) allylmalonate
    3. CAS NO:1227926-43-3
    4. Molecular Formula:
    5. Molecular Weight: 502.993
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1227926-43-3.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: bis(2,4,6-trichlorophenyl) allylmalonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: bis(2,4,6-trichlorophenyl) allylmalonate(1227926-43-3)
    11. EPA Substance Registry System: bis(2,4,6-trichlorophenyl) allylmalonate(1227926-43-3)
  • 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: 1227926-43-3(Hazardous Substances Data)

1227926-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1227926-43-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,9,2 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1227926-43:
(9*1)+(8*2)+(7*2)+(6*7)+(5*9)+(4*2)+(3*6)+(2*4)+(1*3)=163
163 % 10 = 3
So 1227926-43-3 is a valid CAS Registry Number.

1227926-43-3Downstream Products

1227926-43-3Relevant articles and documents

Microwave-assisted synthesis of furo[3,2-c]-1,8-naphthyridines

Guellue, Mustafa,Yigit, Deniz

, p. 1881 - 1888 (2011)

Microwave-assisted ring-conversion reactions of some pyrido[1,2-a] pyrimidine derivatives to 1,8-naphthyridines have been investigated. Novel furo[3,2-c]-1,8-naphthyridine compounds were synthesized in good yields under thermal reaction conditions. Both microwave and classical heating methods have been found to be satisfactory for the synthesis of new 1,8-naphthyridines.

Facile synthesis of novel pyrimido[1,2-a]pyrimidin-4-ones from highly reactive malonates

Guellue, Mustafa,Dincsoenmezl, Ali,Oezyavas, Oeznur

experimental part, p. 2113 - 2120 (2010/06/15)

A very simple and efficient procedure for the synthesis of novel 2-hydrox.y-4H-pyrimido[1,2-a]pyrimidin-4-ones is described. Title compounds were obtained from the room temperature reaction of 2-aminopyrimidine and its substituted derivatives with bis(2,4,6-trichlorophenyl) malonates. High product yields were observed under optimized conditions. Applicability and reactivity of a range of substituted and unsubstituted phenyl malonates were also investigated. Structural identification of all new compounds was accomplished by spectroscopic methods and elemental analysis.

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