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3-Chloro-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridazine is a synthetic chemical compound that belongs to the class of organic compounds known as pyridazines and pyridazine derivatives. It is a member of the pyrazole subclass, characterized by a 5-membered aromatic ring containing three carbon atoms and two nitrogen atoms. The primary structure of 3-CHLORO-6-(3,5-DIMETHYL-1H-PYRAZOL-1-YL)PYRIDAZINE features a (3,5-dimethyl-1H-pyrazol-1-yl)pyridazine core, with a chlorine atom substituted at the 3' position of the pyridazine ring. However, detailed information about its physical characteristics, toxicity, and potential uses is limited or not readily available in the scientific literature.

29334-67-6

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29334-67-6 Usage

Uses

Due to the limited information available, specific applications of 3-CHLORO-6-(3,5-DIMETHYL-1H-PYRAZOL-1-YL)PYRIDAZINE cannot be accurately listed. However, based on its chemical structure and classification, it may potentially be used in various industries such as pharmaceuticals, agrochemicals, or materials science for the development of new compounds with specific properties. Further research and investigation are required to explore its potential applications and establish its safety and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 29334-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,3 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29334-67:
(7*2)+(6*9)+(5*3)+(4*3)+(3*4)+(2*6)+(1*7)=126
126 % 10 = 6
So 29334-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClN4/c1-6-5-7(2)14(13-6)9-4-3-8(10)11-12-9/h3-5H,1-2H3

29334-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-6-(3,5-dimethylpyrazol-1-yl)pyridazine

1.2 Other means of identification

Product number -
Other names 6-(3,5-dimethylpyrazol-1-yl)-3-chloropyridazine

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

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More Details:29334-67-6 SDS

29334-67-6Relevant academic research and scientific papers

Synthesis, crystal structures and properties of two copper (II) complexes with pyridazine derivative ligand

Li, Xiu-Rong,Zhang, Zhi-Hui,Liu, Xiu-Feng,Gao, Hong,Zhang, Xiang-Nan,Fan, Zhi-Jin

, p. 781 - 786 (2008)

Two new complexes, [Cu(L)2(CH3OH)]·(ClO 4)2 (1) and [Cu(L)2(H2O)] ·(NO3)2 (2), have been synthesized and their crystal structures have been determined by X-ray analysis, where L = 3-(3,5-bimethylpyrazole-yl)-6-chloro-pyridazine]. The complex 1 crystallizes in the monoclinic, space group C2/c, and the coordination configuration of copper (II) is better described as trigonal pyramidal geometry with four N atoms from L and one O methanol . The coordination configuration of 2 is quite similar to that of 1 except Owater instead of O methanol . The intermolecular hydrogen bonds link the repeat units and extend the molecules to multinuclear structures in both compounds. The spectral properties of the title compounds have been studied and discussed. Furthermore, the antibacterial activities of the title compounds have been detected, the results indicate that the ligands and two copper(II) complexes exhibit certain fungicidal activities again several bacteria.

Synthesis of Some Novel 2,6-Disubstituted Pyridazin-3(2H)-one Derivatives as Analgesic, Anti-Inflammatory, and Non-Ulcerogenic Agents

Ibrahim, Tamer H.,Loksha, Yasser M.,Elshihawy, Hosam A.,Khodeer, Dina M.,Said, Mohamed M.

, (2017/09/05)

Some novel 2,6-disubstituted pyridazine-3(2H)-one derivatives were synthesized and evaluated for in vitro cyclooxygenase-2 (COX-2) inhibitory efficacy. Compounds 2-{[3-(2-methylphenoxy)-6-oxopyridazin-1(6H)-yl]methyl}-1H-isoindole-1,3(2H)-dione (5a), 2-pr

Synthesis, antibacterial and antioxidant properties of pyrazolylpyridazines

Ather, Abdul Qayuum,Chaudhry, Faryal,Khan, Muhammad Naeem,Bueno, Eliana Aparecida Silicz,Khan, Misbahul Ain,Aslam, Noreen,Khan, Khalid M.,Athar, Muhammad Makshoof,Munawar, Munawar Ali,Ashraf, Muhammad,Ejaz, Syeda Abida

, p. 7743 - 7748 (2013/09/23)

A number of 6-chloro-3-(pyrazol-1′-yl) pyridazines were prepared from 3,6-dichloropyridazine via either reaction with hydrazine followed I by reaction with appropriate reagents to develop the pyrazole or through a nucleophilic reaction with a pyrazole. So

New pyridazine-bridged NHC/pyrazole ligands and their sequential silver(I) coordination

Wimberg, Jan,Scheele, Ulrich J.,Dechert, Sebastian,Meyer, Franc

scheme or table, p. 3340 - 3348 (2011/09/30)

A family of new pyridazine-bridged NHC/pyrazole ligand precursors HL 1-5 were prepared and fully characterized including analysis by XRD {HL1 = 3-[3-(2,6-diisopropylphenyl)-3H-imidazolium-1-yl]-6-(3- pyridin-2-yl-pyrazol-1-yl)-pyrida

Synthesis of amide derivatives of [6-(3,5-dimethylpyrazol-1-yl)-3(2H)- pyridazinone-2-yl]acetic acid and their analgesic and anti-inflammatory properties

Banoglu, Erden,Akoglu, Cagla,Uenlue, Serdar,Erguen, Burcu Caliskan,Kuepeli, Esra,Yesilada, Erdem,Sahin, M. Fethi

, p. 520 - 527 (2007/10/03)

A series of structurally different amide derivatives of [6-(3,5-dimethylpyrazol-1-yl)-3(2H)-pyridazinone-2-yl] acetic acid were prepared and tested for their analgesic and anti-inflammatory activity in vivo by using p-benzoquinone-induced writhing test an

Intramolecular hydrogen bonding between 2-cyanoguanidine and 3-chloro-6-(pyrazol-1-yl)pyridazines in copper(II) complexes

Blake, Alexander J.,Hubberstey, Peter,Li, Wan-Sheung,Russell, Claire E.,Smith, Beverley J.,Wraith, Louise D.

, p. 647 - 655 (2007/10/03)

Treatment of copper(II) salts with 3-chloro-6-(pyrazol-1-yl)pyridazine (cppd)-2-cyanoguanidine (enge) mixtures yielded [Cu(cppd)2(H2O)2[NO3]2, [Cu(cppd)(cnge)2(H2O)(FBF3)][BF4], Cu(cppd)2Cl2·2H2O and Cu(cppd)2Br2· 2H2O. The corresponding 3-chloro-6-(3,5-dimethylpyrazol-1-yl)pyridazine (cmppd) systems gave Cu(cmppd)-(cnge)2(NO3)2·6H2O, [Cu(cmppd)2(cnge)][BF4]2, [Cu(cmppd)(cnge)Cl2]·H2O and Cu(cmppd)(cnge)Br2·H2O. Four of the complexes have been structurally characterised. Whereas the copper atoms in [Cu(cppd)2(H2O)2][NO3]2 and [Cu(cppd)(cnge)2(H2O)(FBF3)][BF4] have tetragonally elongated distorted octahedral geometry, those in [Cu(cmppd)2(cnge)][BF4]2 and [Cu(cmppd)(cnge)Cl2]·H2O adopt trigonal-bipyramidal geometries. The centrosymmetric [Cu(cppd)2(H2O)2]2+ cation comprises two equatorial bidentate chelating cppd ligands and two axial water molecules while [Cu(cppd(cnge)2(H2O)(FBF3)]+ comprises one cppd and two monodentate cnge molecules as equatorial ligands and one water molecule and one BF4- anion as axial ligands. In the [Cu(cmppd)(cnge)Cl2] molecule the chlorine atoms occupy equatorial sites, the cnge an axial position and the cmppd ligand straddles equatorial and axial sites, while in the [Cu(cmppd)2(cnge)]2+ cation the cnge ligand is located equatorially and the two cmppd ligands straddle equatorial and axial sites. Preliminary structural data for Cu(cppd)2Br2·2H2O are consistent with a centrosymmetric tetragonally elongated octahedral copper atom similar to that in [Cu(cppd)2-(H2O)2][NO3]2. Comparable IR and UV/VIS data were obtained for Cu(cmppd)(cnge)2(NO3)2·6H2O and [Cu(cppd)(cnge)2(H2O)(FBF3)][BF4] and for Cu(cmppd)(cnge)Br2·H2O and [Cu(cmppd)(cnge)Cl2]·H2O, suggesting similar molecular structures. Intramolecular N-H ... N hydrogen bonds occur between enge amino groups and pyridazine non-ligating nitrogens in the mixed-ligand complexes [Cu(cppd)(cnge)2(H2O)(FBF3)][BF4] and [Cu(cmppd)(cnge)Cl2]·H2O but not [Cu(cmppd)2(cnge)][BF4]2. That in [Cu(cppd)(cnge)2(H2O)(FBF3)][BF4] differentiates between the two cnge ligands, their different roles being confirmed by the presence of two diagnostic vasym(NCN) doublets in its IR spectrum.

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