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Ethanone, 1-(3-pyridinyl)-, hydrazone (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 280760-19-2 Structure
  • Basic information

    1. Product Name: Ethanone, 1-(3-pyridinyl)-, hydrazone (9CI)
    2. Synonyms: Ethanone, 1-(3-pyridinyl)-, hydrazone (9CI)
    3. CAS NO:280760-19-2
    4. Molecular Formula: C7H9N3
    5. Molecular Weight: 135.16646
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 280760-19-2.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: Ethanone, 1-(3-pyridinyl)-, hydrazone (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(3-pyridinyl)-, hydrazone (9CI)(280760-19-2)
    11. EPA Substance Registry System: Ethanone, 1-(3-pyridinyl)-, hydrazone (9CI)(280760-19-2)
  • 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: 280760-19-2(Hazardous Substances Data)

280760-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 280760-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,0,7,6 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 280760-19:
(8*2)+(7*8)+(6*0)+(5*7)+(4*6)+(3*0)+(2*1)+(1*9)=142
142 % 10 = 2
So 280760-19-2 is a valid CAS Registry Number.

280760-19-2Upstream product

280760-19-2Downstream Products

280760-19-2Relevant articles and documents

Gold(I) complexes bearing ring-fused benzoxazine-derived triazolylidenes and their use in C–N bond-forming processes

Campos-Dominguez, Emmanuel,Vasquez-Perez, Jose,Rojas-Lima, Susana,Lopez-Ruiz, Heraclio,Mendoza-Espinosa, Daniel

, (2020/12/07)

We report the synthesis and full characterization of a novel series of ring-fused benzoxazine-derived triazolium salts (1a–c) and their corresponding triazolylidene gold(I) complexes (2a–c). All new compounds were fully characterized by means of 1H and 13C NMR spectroscopy, elemental analyses, and mass spectroscopy and in the case of triazoliums 1a and 1b by single-crystal X-ray diffraction. The new triazolylidene gold complexes (2a–c) were tested as precatalysts in the hydroamination and hydrohydrazination of terminal alkynes employing aniline derivatives and hydrazine as nitrogen sources, respectively.

Visible-Light-Promoted AuI to AuIII Oxidation in Triazol-5-ylidene Complexes

Mendoza-Espinosa, Daniel,Rendón-Nava, David,Alvarez-Hernández, Alejandro,Angeles-Beltrán, Deyanira,Negrón-Silva, Guillermo E.,Suárez-Castillo, Oscar R.

supporting information, p. 203 - 207 (2017/02/05)

Reaction of triazolium precursors [MIC(CH2)n- H+]I? (n=1–3) with potassium hexamethyldisilazane (KHMDS) and AuCl(SMe2) generates the gold(I) complexes of the type MIC(CH2)n?AuI. Visible light exposure of the latter complexes promotes a spontaneous disproportionation process rendering gold(III) complexes of the type [{MIC(CH2)n}2?AuI2]+I?. Both the AuI and AuIII complex series were tested in the catalytic hydrohydrazination of terminal alkynes using hydrazine as nitrogen source.

Synthesis and Catalytic Benefits of Tetranuclear Gold(I) Complexes with a C4-Symmetric Tetratriazol-5-ylidene

Flores-Jarillo, Mariana,Mendoza-Espinosa, Daniel,Salazar-Pereda, Verónica,González-Montiel, Simplicio

supporting information, p. 4305 - 4312 (2017/11/20)

The facile preparation of a C4-symmteric tetratriazolium salt and its subsequent metalation to generate a series of tetranuclear mesoionic carbene gold(I) complexes is presented. The complete structural characterization of the metallic carbenes

Ancillary ligand-free copper catalysed hydrohydrazination of terminal alkynes with NH2NH2

Peltier, Jesse L.,Jazzar, Rodolphe,Melaimi, Mohand,Bertrand, Guy

supporting information, p. 2733 - 2735 (2016/02/19)

An efficient and selective Cu-catalysed hydrohydrazination of terminal alkynes with parent hydrazine is reported. The methodology tolerates a broad range of functional groups, allows for the synthesis of symmetrical and unsymmetrical azines, and can be extended to hydrazine derivatives and amines.

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