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2,3,4,4,5,6-Hexachloro-2,5-cyclohexadien-1-one is a highly chlorinated and toxic chemical compound, characterized by its pale yellow crystalline solid appearance at room temperature and insolubility in water.

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  • 599-52-0 Structure
  • Basic information

    1. Product Name: 2,3,4,4,5,6-Hexachloro-2,5-cyclohexadien-1-one
    2. Synonyms: 2,3,4,4,5,6-Hexachloro-2,5-cyclohexadien-1-one;Hexachlorocyclohexadienone;USAF DO-65;2,3,4,4,5,6-hexachlorocyclohexa-2,5-dien-1-one
    3. CAS NO:599-52-0
    4. Molecular Formula: C6Cl6O
    5. Molecular Weight: 300.76
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 599-52-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 318.6°C at 760 mmHg
    3. Flash Point: 134°C
    4. Appearance: /
    5. Density: 1.7737 (estimate)
    6. Vapor Pressure: 0.000358mmHg at 25°C
    7. Refractive Index: 1.602
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3,4,4,5,6-Hexachloro-2,5-cyclohexadien-1-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3,4,4,5,6-Hexachloro-2,5-cyclohexadien-1-one(599-52-0)
    12. EPA Substance Registry System: 2,3,4,4,5,6-Hexachloro-2,5-cyclohexadien-1-one(599-52-0)
  • 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: 599-52-0(Hazardous Substances Data)

599-52-0 Usage

Uses

Used in Agricultural Industry:
2,3,4,4,5,6-Hexachloro-2,5-cyclohexadien-1-one is used as an intermediate in the manufacturing of agricultural pesticides, such as hexachlorocyclohexane, due to its ability to contribute to the development of effective pest control agents.
However, it is important to note that 2,3,4,4,5,6-Hexachloro-2,5-cyclohexadien-1-one is also recognized as a persistent organic pollutant in the environment, with the potential to bioaccumulate in living organisms. This poses a significant risk to both human health and the environment, necessitating strict regulations for its use and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 599-52-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 599-52:
(5*5)+(4*9)+(3*9)+(2*5)+(1*2)=100
100 % 10 = 0
So 599-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C6Cl6O/c7-1-3(13)2(8)5(10)6(11,12)4(1)9

599-52-0SDS

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 2,3,4,4,5,6-hexachlorocyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,3,4,4,5,6-hexachlorocyclohexa-2,5-dienone

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:599-52-0 SDS

599-52-0Relevant articles and documents

N-Chloro-2,3,4,4,5,6-hexachlorocyclohexa-2,5-dienylideneamine as a mild and highly regioselective chlorinating reagent

Mamaghani,Zolfigol,Shojaei

, p. 735 - 740 (2007/10/03)

N-Chloro-2,3,4,4,5,6-hexachlorocyclohexa-2,5-dienylideneamine was used as a new, mild and highly regioselective chlorinating reagent in the chlorination of phenol and o-cresol in CCl4, DMF and CH3CN. The effects of C2H5OH, C5H5N, DMF and Et3N on the regioselectivity in CCl4 have also been examined.

NOUVEAUX DECONTAMINANTS. DESTRUCTION CHIMIQUE DU PARAOXON ET DU PARATHION AU MOYEN DE COMPOSES A CHLORE POSITIF

Hedayatullah, Mir,Lion, Claude,Tourki, Amel

, p. 281 - 292 (2007/10/02)

The use of compounds possessing positive chlorine and precursors of hypochlorite anions, with different micellar systems, permits the very rapid and complete destruction of paraoxon and parathion taken as models of insecticides or potent chemical warfare

HALOGENATION REGIOSELECTIVE EN SERIE AROMATIQUE-I CHLORATION DES PHENOLS ET LEURS ETHERS A L'AIDE DE REACTIFS METTANT EN JEU DES INTERACTIONS DONNEUR-ACCEPTEUR

Guy, Alain,Lemaire, Marc,Guette, Jean-Paul

, p. 2339 - 2346 (2007/10/02)

An efficient regiospecific route for the chlorination of phenol involving hexachlorohexadienones is described.The selectivity is attained by using a reagent tailored in such a way that it is able to participate in charge transfer interactions and hydrogen bonding with the substrate.This recognition between substrate (phenol) and 2,3,4,4,5,6-hexachlorocyclohexa 2,5-dien 1-one 1 which we called "reactif p" allows the chlorination of phenol in the para position.The use of 2,3,4,5,6,6-hexachlorocyclohexa 2,4-dien-1 one 2 we have called "reactif o" permits the chlorination in the ortho position.These two reagents are stable and inexpensive materials, synthetized from pentachlorophenol and chlorine.The chlorination of anisole with these two reagents, gives solely the parachloro derivative, under steric control.

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