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2,2,4,4,6-Pentachloro-5-cyclohexen-1,3-dione, also known as pentachlorocyclohexadienedione, is a chemical compound with the molecular formula C6Cl5O2. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. 2,2,4,4,6-pentachloro-5-cyclohexen-1,3-dione is a derivative of cyclohexen-1,3-dione, with five chlorine atoms replacing hydrogen atoms on the cyclohexene ring. It is primarily used as an intermediate in the synthesis of various chemicals, including pesticides and herbicides. Due to its chemical structure, it exhibits strong electrophilic properties, which makes it reactive with nucleophiles. However, it is important to note that 2,2,4,4,6-pentachloro-5-cyclohexen-1,3-dione may have potential health and environmental risks, and proper handling and disposal procedures should be followed when working with it.

15679-05-7

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15679-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15679-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,7 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15679-05:
(7*1)+(6*5)+(5*6)+(4*7)+(3*9)+(2*0)+(1*5)=127
127 % 10 = 7
So 15679-05-7 is a valid CAS Registry Number.

15679-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4,4,6-pentachloro-5-cyclohexen-1,3-dione

1.2 Other means of identification

Product number -
Other names 2,2,4,6,6-pentachloro-cyclohex-4-ene-1,3-dione

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:15679-05-7 SDS

15679-05-7Relevant academic research and scientific papers

Reactions of resorcinol and its chlorinated derivatives with monochloramine: Identification of intermediates and products

Heasley, Victor L.,Alexander, Michael B.,Deboard, Ryan H.,Hanley Jr., John C.,Mckee, Tawnya C.,Wadley, Brian D.,Shellhamer, Dale F.

, p. 2406 - 2409 (1999)

An investigation of the reaction of resorcinol (compound 1) and its chlorinated derivatives 4-chlororesorcinol (compound 4), 4,6- dichlororesorcinol (compound 5), and 2,4,6-trichlororesorcinol (compound 2) with monochloramine (NH2Cl) in ether and aqueous solution (pH 7) is reported. NH2Cl reacted with compounds 1, 2, 4, and 5 to give the pentachloro intermediate, 2,2,4,4,6-pentachloro-5-cyclohexen-1,3-dione (compound 3), which underwent ring opening with H2O and loss of CO2 in the presence of NH2Cl to produce the following: 1,1,3,5,5-pentachloro-3-penten- 2-one (compound 6), 1,1,1,3,5,5-hexachloro-3-penten-2-one (compound 7), and 1,1,3,5,5,5-hexachloro-3-penten-2-one (compound 8). Compound 6 reacted further with NH2Cl to give compounds 7 and 8; in the presence of NH2Cl, compound 7 rearranged to compound 8. Mechanisms for the preceding reactions are analyzed in detail. Another aspect of the investigation involved a determination of the amounts of chloroform, CHCl3, which is produced from compound 3 with NH2Cl (4%) and with NaOCl (50%). The low production of CHCl3 from compound 3 and NH2Cl is discussed in connection with the probable reactions of compounds 7 and 8 with NH2Cl and H2O.

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