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1,4,5,6,7,7-Hexachlorobicyclo(2.2.1)-5-heptene-2,3-dicarboxylic acid, also known as Hexachlorocyclohexane (HCH) isomer γ-HCH, is a chemical compound belonging to the family of organochlorine pesticides. It is a white crystalline solid with a chemical formula of C7H6Cl6O4. γ-HCH is one of the eight isomers of HCH, which is a broad-spectrum insecticide used to control various pests in agriculture and public health. However, due to its persistence in the environment, bioaccumulation in the food chain, and potential adverse effects on human health and the environment, the production and use of HCH, including γ-HCH, have been banned or restricted in many countries under the Stockholm Convention on Persistent Organic Pollutants.

7374-78-9

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7374-78-9 Usage

Appearance

White, crystalline solid

Primary use

Flame retardant

Applications

Electrical insulating materials
Unsaturated polyester resins
Epoxy resins

Additional uses

Curing agent for epoxy resins
Corrosion inhibitor
Crosslinking agent in elastomers and plastics

Environmental classification

Persistent organic pollutant

International regulations

Subject to the Stockholm Convention on Persistent Organic Pollutants

Check Digit Verification of cas no

The CAS Registry Mumber 7374-78-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,7 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7374-78:
(6*7)+(5*3)+(4*7)+(3*4)+(2*7)+(1*8)=119
119 % 10 = 9
So 7374-78-9 is a valid CAS Registry Number.

7374-78-9Downstream Products

7374-78-9Relevant academic research and scientific papers

Phase transfer catalysis by tetraethylammonium bromide: Nucleophilic opening of anhydrides using potassium superoxide in aprotic medium

Singh, Sundaram,Shukla, Ajay Kumar,Singh, Krishna Nand

, p. 1184 - 1188 (2007/10/03)

Tetraethylammonium superoxide, generated in situ by the phase transfer reaction of potassium superoxide and tetraethylammonium bromide, brings about a clean cleavage of various anhydrides, particularly those with high molecular weight in dry dimethylformamide. As an outcome, succinic anhydride 1; glutaric anhydride 2; 3,3-dimethylglutaric anhydride 3; phthalic anhydride 4; diphenic anhydride 5; 1,2,3,4-tetrahydro-9-oxo-1,4-ethanonaphthalene-2,3- endo-dicarboxylic anhydride 6: 1,4,5,6,7,7-hexachloro-5-norbomene-2,3- dicarboxylic anhydride 7; endo-bicyclo [2.2.1] heptan-2-one-5,6-dicarboxylic anhydride 8; cis-5-norbornene-endo-2,3-dicarboxylic anhydride 9 and trans- 1,2-cyclohexane dicarboxylic anhydride 10 have been transformed into their corresponding dicarboxylic acids in fairly good yields. The report demonstrates the applicability of tetraethylammonium bromide as a phase transfer catalyst for efficient superoxide studies.

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