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5355-83-9

3,5,8,10-Tetrachloro-1,6-pyrenedione is a chemical compound with the molecular formula C16H4Cl4O2. It is a derivative of pyrene, a polycyclic aromatic hydrocarbon, with four chlorine atoms attached to the 3, 5, 8, and 10 positions of the molecule. 3,5,8,10-tetrachloro-1,6-pyrenedione is known for its potential environmental and health impacts, as it can be formed during the combustion of materials containing chlorine, such as plastics and other synthetic materials. Due to its persistence and potential toxicity, it is a subject of interest in environmental chemistry and toxicology studies. The compound's properties, such as its stability, solubility, and reactivity, are influenced by the presence of the chlorine atoms, which can also affect its behavior in the environment and its potential to bioaccumulate in living organisms.

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  • 5355-83-9 Structure

  • Basic information

    1. Product Name: 3,5,8,10-tetrachloro-1,6-pyrenedione
    2. Synonyms: 3,5,8,10-tetrachloro-1,6-pyrenedione
    3. CAS NO:5355-83-9
    4. Molecular Formula: C16H4Cl4O2
    5. Molecular Weight: 370.01376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5355-83-9.mol

  • Chemical Properties

    1. Melting Point: 315-320 °C
    2. Boiling Point: 497.7°Cat760mmHg
    3. Flash Point: 254.8°C
    4. Appearance: /
    5. Density: 1.28g/cm3
    6. Vapor Pressure: 1.49E-09mmHg at 25°C
    7. Refractive Index: 1.57
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3,5,8,10-tetrachloro-1,6-pyrenedione(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,5,8,10-tetrachloro-1,6-pyrenedione(5355-83-9)
    12. EPA Substance Registry System: 3,5,8,10-tetrachloro-1,6-pyrenedione(5355-83-9)

  • 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: 5355-83-9(Hazardous Substances Data)

5355-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5355-83-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5355-83:
(6*5)+(5*3)+(4*5)+(3*5)+(2*8)+(1*3)=99
99 % 10 = 9
So 5355-83-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H21BrN2O2/c1-12-14(3)18(19)15(4)13(2)17(12)11-23-20-21(22)10-16-8-6-5-7-9-16/h5-9H,10-11H2,1-4H3/b21-20-

5355-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5,8,10-tetrachloropyrene-1,6-dione

1.2 Other means of identification

Product number -
Other names 3,5,8,10-Tetrachlor-pyren-1,6-dion

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:5355-83-9 SDS

5355-83-9Relevant articles and documents

NAPHTHALENE DIIMIDE COMPOUNDS INTERACTING WITH G-QUADRUPLEX REGIONS IN DNA

-

, (2009/07/03)

The invention relates to novel compounds which are naphthalene diimides of general formula (I). The compounds are used in therapy, particularly in cancer treatment.

Tri- and tetra-substituted naphthalene diimides as potent G-quadruplex ligands

Cuenca, Francisco,Greciano, Olga,Gunaratnam, Mekala,Haider, Shozeb,Munnur, Deeksha,Nanjunda, Rupesh,Wilson, W. David,Neidle, Stephen

, p. 1668 - 1673 (2008/12/21)

A series of tri- and tetra-substituted naphthalene diimides have been designed and synthesized. Several compounds show exceptional affinity for telomeric G-quadruplex DNA in classical and competition FRET assays and SPR studies. They inhibit telomerase in the TRAP assay, and show potent senescence-based short-term anti-proliferative effects on MCF7 and A549 cancer cell lines, and localize in the nucleus and particularly the nucleolus of MCF7 cells.

Synthesis and optical and redox properties of core-substituted naphthalene diimide dyes

Thalacker, Christoph,Roeger, Cornelia,Wuerthner, Frank

, p. 8098 - 8105 (2007/10/03)

2,6-Dichloronaphthalene dianhydride has been synthesized by a modified procedure. The imidization of this dichlorinated anhydride with amines and subsequent stepwise nucleophilic exchange of the chlorine atoms by alkyl- or arylamines afforded a series of hitherto unknown monoamino- and diamino-substituted naphthalene diimides. An alternative route for the synthesis of diamino-substituted naphthalene diimides is also reported. Optical and electrochemical properties of the newly synthesized amino-functionalized naphthalene diimides were studied in detail. The absorption maxima (530-620 nm) of these dyes are appreciably bathochromically shifted compared to those of the corresponding core-unsubstituted compounds. At the naphthalene core alkylamino-substituted diimides exhibit fluorescence quantum yields up to 60%.

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