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Methanone, 3,6-pyridazinediylbis[phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135034-09-2 Structure
  • Basic information

    1. Product Name: Methanone, 3,6-pyridazinediylbis[phenyl-
    2. Synonyms:
    3. CAS NO:135034-09-2
    4. Molecular Formula: C18H12N2O2
    5. Molecular Weight: 288.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135034-09-2.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: Methanone, 3,6-pyridazinediylbis[phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methanone, 3,6-pyridazinediylbis[phenyl-(135034-09-2)
    11. EPA Substance Registry System: Methanone, 3,6-pyridazinediylbis[phenyl-(135034-09-2)
  • 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: 135034-09-2(Hazardous Substances Data)

135034-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135034-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,3 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135034-09:
(8*1)+(7*3)+(6*5)+(5*0)+(4*3)+(3*4)+(2*0)+(1*9)=92
92 % 10 = 2
So 135034-09-2 is a valid CAS Registry Number.

135034-09-2Downstream Products

135034-09-2Relevant articles and documents

Pyridazines. LXVIII. Convenient synthesis of phenyl (6-substituted 3- pyridazinyl) ketones via the oxidative decyanation route

Heinisch,Langer

, p. 1685 - 1690 (1993)

A convenient approach to aryl 3-pyridazinyl ketones 4, 7-10 bearing various O-, N-, or C-substituents at C-6 of the diazine nucleus via oxidative decyanation of appropriate aryl-heteroaryl-acetonitriles is proposed.

Synthesis of 3,6-Disubstituted Pyridazine Derivatives

Mernari, Bouchaib,Lagrenee, Michel

, p. 2059 - 2061 (1996)

The synthesis of pyridazine functionalized with dioximes side chains are described. Several 3,6-disubstituted pyridazine derivatives were prepared and their structures determined by spectroscopic methods (nmr, ir and ms).

Dicopper(II) Complexes of Novel Polyfunctional Pyridazines: Crystal Structure and Magnetic Properties of Bis1,N':N2,N">-bis

Abraham, Francis,Lagrenee, Michel,Sueur, Stephane,Mernari, Bouchaib,Bremard, Claude

, p. 1443 - 1447 (2007/10/02)

Two novel pyridazine ligands with 3,6-CR=NOH (R = H, H2L1; Ph, H2L2) oxime side chains were synthesised. the related copper(II) dinuclear complexes 1)2(ClO4)2(H2O)2> 1 and 2)2(ClO4)2(MeOH)n> 2 were obtained subsequently.The crystal structure of 1 was determined: space group P21/n, a=12.031(6), b=9.517(4), c=9.973(5) Angstroem, β=100.16 deg and Z=2.The copper(II) ions of the binuclear unit are bridged by the two diazine fragments of the two essentially planar tetradentate ligands with the oxime nitrogen atoms completing the equatorial co-ordination.Two intra-complex hydrogen bridges link the terminal oximato moieties to give dinucleating macrocyclic complexes.In complexes 1 and 2 the copper(II) is in a classical 4 + 2 environment.The magnetic properties of those compounds revealed a spin-singlet ground state in each case.The singlet-triplet energy gaps were found to be -536(2) for 1 and -545(4) cm-1 for 2.The low-lying states of the complexes are discussed in relation to the nearly planar structure of the macrocyclic complexes.

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