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1,2-Benzenedicarbonitrile, 4-(3-pyridinyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93485-73-5 Structure
  • Basic information

    1. Product Name: 1,2-Benzenedicarbonitrile, 4-(3-pyridinyloxy)-
    2. Synonyms: 4-pyrid-3-yloxyphthalonitrile;
    3. CAS NO:93485-73-5
    4. Molecular Formula: C13H7N3O
    5. Molecular Weight: 221.218
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93485-73-5.mol
  • Chemical Properties

    1. Melting Point: 111 °C(Solv: ethanol (64-17-5))
    2. Boiling Point: 427.4±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.30±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2-Benzenedicarbonitrile, 4-(3-pyridinyloxy)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Benzenedicarbonitrile, 4-(3-pyridinyloxy)-(93485-73-5)
    11. EPA Substance Registry System: 1,2-Benzenedicarbonitrile, 4-(3-pyridinyloxy)-(93485-73-5)
  • 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: 93485-73-5(Hazardous Substances Data)

93485-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93485-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,8 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93485-73:
(7*9)+(6*3)+(5*4)+(4*8)+(3*5)+(2*7)+(1*3)=165
165 % 10 = 5
So 93485-73-5 is a valid CAS Registry Number.

93485-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-pyridin-3-yloxybenzene-1,2-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 4-pyrid-3-yloxyphthalonitrile

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:93485-73-5 SDS

93485-73-5Downstream Products

93485-73-5Relevant articles and documents

Gaining Access to Bacteria through (Reversible) Control of Lipophilicity

Galstyan, Anzhela,Putze, Johannes,Dobrindt, Ulrich

, p. 1178 - 1186 (2018)

The development of antimicrobial photodynamic therapy (aPDT) is highly dependent on the development of suitable photosensitizers (PSs); ideally, affinity of a PS towards bacterial cells should be much higher than that towards mammalian cells. A cationic c

Photodynamic efficacy of water-soluble Si(IV) and Ge(IV) phthalocyanines towards Candida albicans planktonic and biofilm cultures

Mantareva, Vanya,Angelov, Ivan,Kussovski, Veselin,Dimitrov, Roumen,Lapok, Lukasz,W?hrle, Dieter

, p. 4430 - 4440 (2011)

Water-soluble phthalocyanine complexes of silicon (SiPc1) and germanium (GePc1) were synthesized. The absorbance of SiPc1 in water was with minor aggregation while GePc1 strongly aggregated in water. The fluorescence data in water showed low quantum yield

Boronic Acid Functionalized Photosensitizers: A Strategy To Target the Surface of Bacteria and Implement Active Agents in Polymer Coatings

Galstyan, Anzhela,Schiller, Roswitha,Dobrindt, Ulrich

, p. 10362 - 10366 (2017)

Advanced methods for preventing and controlling hospital-acquired infections via eradication of free-floating bacteria and bacterial biofilms are of great interest. In this regard, the attractiveness of unconventional treatment modalities such as antimicr

Absorption and electrochemical properties of cobalt and iron phthalocyanines and their quaternized derivatives: Aggregation equilibrium and oxygen reduction electrocatalysis

Tasso, Thiago Teixeira,Furuyama, Taniyuki,Kobayashi, Nagao

, p. 9206 - 9215 (2013)

The synthesis and investigation of the electronic properties of Co(II) and Fe(II)tetrakis(pyridine-3-yloxy)phthalocyanines, as well as the respective quaternized complexes, are reported here. After quaternization reaction, the compounds showed increased s

Umbelliferone Decorated Water-soluble Zinc(II) Phthalocyanines – In Vitro Phototoxic Antimicrobial Anti-cancer Agents

Sowa, Andrea,H?ing, Alexander,Dobrindt, Ulrich,Knauer, Shirley K.,Galstyan, Anzhela,Voskuhl, Jens

supporting information, p. 14672 - 14680 (2021/09/18)

In this contribution we report on the synthesis, characterization and application of water-soluble zinc(II) phthalocyanines, which are decorated with four or eight umbelliferone moieties for photodynamic therapy (PDT). These compounds are linked periphera

Novel nitrogen-containing heteroaryl compounds and methods of use thereof

-

Page 67, (2008/06/13)

The present invention relates to compounds suitable for use in mediating hypoxia inducible factor and for treating erythropoietin-associated conditions by increasing endogenous erythropoietin in vitro and in vivo.

A New Method for the Synthesis of Zinc Tetrakis-(3-methylpyridyloxy)-phthalocyanine and the Physical Properties of Dimers formed by Complexation of the Cationic Phthalocyanine with Anionic Porphyrins

Gaspard, Serge,Tran-Thi, Thu-Hoa

, p. 383 - 390 (2007/10/02)

Face-to-face heterodimers have been obtained by pairing a cationic phthalocyanine with two different anionic, metal-free and manganese(III) porphyrins.Different behaviour has been observed for the spectroscopic and fluorescence properties of the dimers.Fo

SYNTHESIS AND CHARACTERIZATION OF 2,9,16,23-TETRA(3-PYRIDYLOXY)PHTHALOCYANINE IN THE FORM OF ITS ZINC(II) CHELATE

Oliver, Stuart W.,Smith, Thomas D.

, p. 2047 - 2052 (2007/10/02)

2,9,16,23-Tetra(3-pyridyloxy)phthalocyanine has been prepared by the reaction of lithium chloride with 5-(pyridyloxy)-1,3-diiminoisoindoline in 2-(dimethylamino)ethanol solution followed by demetallation.The zinc chelate of the phthalocyanine has been prepared in a similar condensation reaction using zinc chloride.

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