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3-formylphenyl boronic acid diethanolamine ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1227678-05-8 Structure
  • Basic information

    1. Product Name: 3-formylphenyl boronic acid diethanolamine ester
    2. Synonyms:
    3. CAS NO:1227678-05-8
    4. Molecular Formula:
    5. Molecular Weight: 219.048
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1227678-05-8.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: 3-formylphenyl boronic acid diethanolamine ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-formylphenyl boronic acid diethanolamine ester(1227678-05-8)
    11. EPA Substance Registry System: 3-formylphenyl boronic acid diethanolamine ester(1227678-05-8)
  • 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: 1227678-05-8(Hazardous Substances Data)

1227678-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1227678-05-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,6,7 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1227678-05:
(9*1)+(8*2)+(7*2)+(6*7)+(5*6)+(4*7)+(3*8)+(2*0)+(1*5)=168
168 % 10 = 8
So 1227678-05-8 is a valid CAS Registry Number.

1227678-05-8Downstream Products

1227678-05-8Relevant articles and documents

Preparation of a novel group of hybrid compounds N-benzyl aminoboronbenzylphosphonic and N,N′-ethylenedi(aminoboronbenzylphosphonic) acids

M?ynarz, Piotr,Rydzewska, Agata,Pok?adek, Ziemowit

, p. 457 - 460 (2011)

Two groups of new boronic acids containing aminophosphonate functions were synthesized and characterized by NMR spectroscopy and ESI-MS. Both groups of compounds were obtained by simple reactions of prepared in situ tris(trimethylsilyl) phosphite with a corresponding imine. The synthesized compounds may serve as a potential new class of building blocks, BNCT agents and supramolecular host molecules.

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