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methyl 2-(4-{[(2-hydroxyphenyl)amino]methyl}-1H-1,2,3-triazol-1-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1571119-54-4 Structure
  • Basic information

    1. Product Name: methyl 2-(4-{[(2-hydroxyphenyl)amino]methyl}-1H-1,2,3-triazol-1-yl)acetate
    2. Synonyms: methyl 2-(4-{[(2-hydroxyphenyl)amino]methyl}-1H-1,2,3-triazol-1-yl)acetate
    3. CAS NO:1571119-54-4
    4. Molecular Formula:
    5. Molecular Weight: 262.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1571119-54-4.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: methyl 2-(4-{[(2-hydroxyphenyl)amino]methyl}-1H-1,2,3-triazol-1-yl)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-(4-{[(2-hydroxyphenyl)amino]methyl}-1H-1,2,3-triazol-1-yl)acetate(1571119-54-4)
    11. EPA Substance Registry System: methyl 2-(4-{[(2-hydroxyphenyl)amino]methyl}-1H-1,2,3-triazol-1-yl)acetate(1571119-54-4)
  • 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: 1571119-54-4(Hazardous Substances Data)

1571119-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1571119-54-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,1,1,1 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1571119-54:
(9*1)+(8*5)+(7*7)+(6*1)+(5*1)+(4*1)+(3*9)+(2*5)+(1*4)=154
154 % 10 = 4
So 1571119-54-4 is a valid CAS Registry Number.

1571119-54-4Downstream Products

1571119-54-4Relevant articles and documents

Rhenium Complexes Based on an N2O Tridentate Click Scaffold: From Synthesis, Structural and Theoretical Characterization to a Radiolabelling Study

Eychenne, Romain,Guizani, Sihem,Wang, Jin-Hui,Picard, Claude,Malek, Nadia,Fabre, Paul-Louis,Wolff, Mariusz,Machura, Barbara,Saffon, Nathalie,Lepareur, Nicolas,Benoist, Eric

, p. 69 - 81 (2017)

A general synthetic approach to a novel range of semirigid bifunctional chelating agents (BCAs) that include an aromatic ring and a triazolyl moiety in the chelating unit has been investigated for the fac-[M(CO)3]+core (M =185/187Re or188Re). The strategy includes the facile preparation of these N2O ligands bearing various functionalized arms (carboxylate, terminal alkyne, aromatic amine). The reaction of commercial [Re(CO)5Cl] {or a freshly prepared [Re(OH2)3(CO)3]+precursor} with our BCAs in methanol led to the formation of stable neutral tricarbonylrhenium complexes of general formula [Re(CO)3(L)] (LH = 5, 10, 11) in high yields. These compounds were characterized by IR and NMR spectroscopy, mass spectrometry, electrochemistry, and X-ray crystallography for [Re(CO)3(5–H)] and [Re(CO)3(11–H)] as well as by DFT calculations. The analogous rhenium-188 complexes [188Re(CO)3(5)] and [188Re(CO)3(11–H)] were also prepared, in acceptable to excellent yields, by the reaction of 5 or 11 with the fac-[188Re(OH2)3(CO)3]+precursor in methanol at 80 °C. The structural identities of the radioactive complexes were assessed by HPLC studies. The good affinity of these click ligands for the ReIcore combined with the ease of their derivatization make this chelating system promising for the conception of target-specific radiopharmaceuticals for therapeutic purposes.

Synthesis and preliminary biological evaluation of the first 99mTc(I)-specific semi-rigid tridentate ligand based on a click chemistry strategy

Guizani, Sihem,Malek Saied, Nadia,Picard, Claude,Benoist, Eric,Saidi, Mouldi

, p. 158 - 163 (2014)

A novel bifunctional chelating agent based on a click chemistry strategy has been synthesized and characterized on the basis of spectroscopic techniques. The metal chelating part of this new class of tridentate N2O ligand combined a triazole un

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