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Pyridazine, 3,6-diethynyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160510-67-8 Structure
  • Basic information

    1. Product Name: Pyridazine, 3,6-diethynyl- (9CI)
    2. Synonyms: Pyridazine, 3,6-diethynyl- (9CI)
    3. CAS NO:160510-67-8
    4. Molecular Formula: C8H4N2
    5. Molecular Weight: 128.13076
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160510-67-8.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: Pyridazine, 3,6-diethynyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyridazine, 3,6-diethynyl- (9CI)(160510-67-8)
    11. EPA Substance Registry System: Pyridazine, 3,6-diethynyl- (9CI)(160510-67-8)
  • 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: 160510-67-8(Hazardous Substances Data)

160510-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160510-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,5,1 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 160510-67:
(8*1)+(7*6)+(6*0)+(5*5)+(4*1)+(3*0)+(2*6)+(1*7)=98
98 % 10 = 8
So 160510-67-8 is a valid CAS Registry Number.

160510-67-8SDS

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 3,6-bis(ethynyl)pyridazine

1.2 Other means of identification

Product number -
Other names 3,6-diethynylpyridazine

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:160510-67-8 SDS

160510-67-8Relevant articles and documents

Isomeric platinum organometallics derived from pyrimidine, pyridazine or pyrazine and their potential as antitumor drugs

Singh, Khushwant,Jana, Achintya,Lippmann, Petra,Ott, Ingo,Das, Neeladri

, p. 112 - 117 (2019)

Two new organometallic compounds (1 and 2) containing multiple platinum(II) centers have been synthesized. 1 and 2 are structural isomers having the same molecular formula but they are different either in terms of the N-heterocycle present in the center or relative orientation of the two pendant arms bearing the alkynyl-Pt(PEt3)2I units. 1 and 2 have been characterized using FTIR, NMR, HRMS and elemental analyses, besides structural characterization of one of the complex (1) using single crystal XRD. The cytotoxic potential of 1 and 2 and a previously reported di-PtII organometallic molecule (3) have been studied against four cancer cell lines – HT-29 (colon carcinoma), MCF-7, MDA-MB-231 (breast cancer) and SK-HEP-1 (human hepatic adenocarcinoma). Comparison of IC50 values suggests that these Pt(II) based organometallic compounds have antiproliferative activity that is comparable with that of cisplatin.

Click Chemistry Derived Pyridazines: Electron-Deficient Building Blocks with Defined Conformation and Packing Structure

Birkenfelder, Irén,Gurke, Johannes,Grubert, Lutz,Hecht, Stefan,Schmidt, Bernd M.

supporting information, p. 3156 - 3161 (2017/11/23)

A series of 3,6-bis(4-triazolyl)pyridazines equipped with terminal phenyl substituents with varying degree of fluorination were synthesized by using the facile copper-catalyzed azide–alkyne cycloaddition and their structures were thoroughly investigated i

Self-assembly of 3,6-bis(4-triazolyl)pyridazine ligands with copper(I) and silver(I) ions: Time-dependant 2D-NOESY and ultracentrifuge measurements

Happ, Bobby,Pavlov, Georges M.,Altuntas, Esra,Friebe, Christian,Hager, Martin D.,Winter, Andreas,Goerls, Helmar,Guenther, Wolfgang,Schubert, Ulrich S.

experimental part, p. 873 - 880 (2011/10/08)

Two 3,6-bis(R-1H-1,2,3-triazol-4-yl)pyridazines (R=mesityl, monodisperse (CH2-CH2O)12CH3) were synthesized by the copper(I)-catalyzed azide-alkyne cycloaddition and self-assembled with tetrakis(acetonitrile)copp

5b,7b-diaza-3b,9b-diborabenzo[ghi]perylenes

Bosdet, Michael J.D.,Piers, Warren E.,Sorensen, Ted S.,Parvez, Masood

experimental part, p. 426 - 433 (2010/09/16)

Treatment of a precursor to the chelating Lewis acid 2,2′- diborabiphenyl with 2,6-bisalkynyl-substituted pyridazines, leads to elimination of 2 equiv. of ClSiMe3; subsequent treatment of the mixture with PtCl2 catalyzes the cyclizat

Oligomers containing ethynylpyridazine moieties: Synthesis, fluorescence and liquid crystalline properties. Diazines 50

Achelle, Sylvain,Ple, Nelly,Kreher, David,Mathevet, Fabrice,Turck, Alain,Attias, Andre-Jean

, p. 357 - 374 (2008/09/20)

Conjugated oligomers with ethynylpyridazine units have been synthetized by Sonogashira and Suzuki cross-coupling reactions. Some of them present interesting liquid crystals properties investigated by differential scanning calorimetry (DSC) and polarized l

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