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101342-95-4

di-2-pyridyl ketone benzoylhydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101342-95-4 Structure

  • Basic information

    1. Product Name: di-2-pyridyl ketone benzoylhydrazone
    2. Synonyms:
    3. CAS NO:101342-95-4
    4. Molecular Formula: C18H14N4O
    5. Molecular Weight: 302.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101342-95-4.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: di-2-pyridyl ketone benzoylhydrazone(CAS DataBase Reference)
    10. NIST Chemistry Reference: di-2-pyridyl ketone benzoylhydrazone(101342-95-4)
    11. EPA Substance Registry System: di-2-pyridyl ketone benzoylhydrazone(101342-95-4)

  • 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: 101342-95-4(Hazardous Substances Data)

101342-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101342-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,3,4 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101342-95:
(8*1)+(7*0)+(6*1)+(5*3)+(4*4)+(3*2)+(2*9)+(1*5)=74
74 % 10 = 4
So 101342-95-4 is a valid CAS Registry Number.

101342-95-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(dipyridin-2-ylmethylideneamino)benzamide

1.2 Other means of identification

Product number -
Other names bis(2-pyridyl)ketone benzoylhydrazone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:101342-95-4 SDS

101342-95-4Relevant articles and documents

Synthesis, spectroscopic, crystal structures and photoluminescence studies of cadmium(II) complexes derived from di-2-pyridyl ketone benzoylhydrazone: Crystal structure of a rare eight coordinate cadmium(II) complex

Kuriakose, Daly,Aravindakshan, A. Ambili,Kurup, M.R. Prathapachandra

, p. 84 - 96 (2017)

Four cadmium(II) complexes, [CdL2] (1), [Cd(HL)Cl2] (2), [Cd(HL)Br2] (3) and [Cd(HL)(NO3)2(H2O)] (4) of di-2-pyridyl ketone benzoylhydrazone (HL) have been synthesized and characterized by

Synthesis, spectroscopic and X-ray crystallographic properties of manganese compounds of keto- and enol-coordinated di-2-pyridyl ketone benzoyl hydrazone (dpkbh). Reactions of [Mn(CO)5Br] with dpkbh

Bakir, Mohammed,Conry, Rebecca

, p. 1244 - 1257 (2016)

Reactions between [Mn(CO)5Br] and dpkbh in low boiling solvents in air gave fac-[MnI(CO)3(Κ2-Npy,Nim-dpkbh)Br]·H2O, [MnIIBr2(Κ3-Npy,N

Molecular structure and optosensing behavior of di-2-pyridyl ketone benzoylhydrazone in non-aqueous solvents

Bakir, Mohammed,Brown, Ordel

, p. 129 - 136 (2002)

Crystals of di-2-pyridyl ketone benzoylhydrazone (dpkbh) obtained from a dimethylsulfoxide (DMSO) solution of dpkbh are in the monoclinic space group, Pl/c. Structural analysis reveals anti-parallel, non-planar, one-dimensional tapes of dpkbh w

Stability, Stoichiometry, and Structure of Fe(II) and Fe(III) Complexes with Di-2-pyridyl Ketone Benzoylhydrazone: Environmental Applications

Iha, Maria E. V. Suarez,Pehkonen, Simo O.,Hoffmann, Michael R.

, p. 2080 - 2086 (1994)

The stoichiometry, structure, and thermodynamics of Fe(II) and Fe(III) complexes of di-2-pyridyl ketone benzoylhydrazone (DPKBH) were studied at pH 5.3 and 25.0 deg C in water-ethanol solutions. The spectrophotometric method of corresponding solutions was

Coordination of bidentate aroylhydrazone-based N,N-Donor ligands to the fac-[re(co)3]+ core

Mukiza, Janvier,Gerber, Thomas I. A.,Hosten, Eric C.

, p. 368 - 375 (2014)

The reaction of the potentially bidentate aroylhydrazone-based N,N-donor ligands N-(di(pyridin-2-yl)-methylene)benzohydrazide (Hdpmb) and 3-((pyridin-2-yl)methyleneamino)-2,3-dihydro-2-(pyridin-2-yl)quinazolin-4-(1H) one (Hppq) with [Re(CO)5Cl]

Evaluating the role of a urea-like motif in enhancing the thermal and mechanical strength of supramolecular gels

Tómasson, Daníel Arnar,Ghosh, Dipankar,Kurup, M. R. Prathapachandra,Mulvee, Matthew T.,Damodaran, Krishna K.

, p. 617 - 628 (2021/02/03)

The geometry and spatial orientation of gelator molecules and the mode of various intermolecular non-covalent interactions are the key parameters that dictate the structure and properties of low molecular weight gelators (LMWGs). The effect of intermolecu

METAL ION CHELATORS AND THERAPEUTIC USE THEREOF

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Page 37, (2008/06/13)

The present invention relates to compounds which are capable of chelating metal ions. In particular, the present invention relates to (thio)semicarbazone compounds and (thio)hydrazone compounds which are capable of chelating metal ions, including iron ions. Also disclosed are therapeutic use of such compounds and/or their metal ion complexes, including methods of treating diseases associated with cell proliferation.

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