877-08-7 Usage
Description
1,2,3,4-Tetrachloro-5,6-Dimethylbenzylene is a powdered or flaked solid that is insoluble in water. It is a strongly irritating chemical that can cause severe irritation to the skin, eyes, or mucous membranes. Ingestion of this substance may also be toxic.
Uses
1,2,3,4-Tetrachloro-5,6-Dimethylbenzylene is used in various applications across different industries, including:
Used in Chemical Industry:
1,2,3,4-Tetrachloro-5,6-Dimethylbenzylene is used as a chemical intermediate for the synthesis of various organic compounds and polymers. Its unique structure with four chlorine atoms and two methyl groups allows it to be a versatile building block in the production of various chemicals.
Used in Pharmaceutical Industry:
1,2,3,4-Tetrachloro-5,6-Dimethylbenzylene is used as a starting material in the development of new pharmaceutical compounds. Its chemical properties make it suitable for the synthesis of drugs with potential therapeutic applications.
Used in Agrochemical Industry:
1,2,3,4-Tetrachloro-5,6-Dimethylbenzylene is used as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its ability to form stable compounds with other elements makes it a valuable component in the development of effective crop protection products.
Used in Dye and Pigment Industry:
1,2,3,4-Tetrachloro-5,6-Dimethylbenzylene is used as a key component in the synthesis of dyes and pigments. Its chemical structure allows it to be incorporated into various colorants, providing a wide range of hues and shades for various applications.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Simple aromatic halogenated organic compounds, such as TETRACHLORO-O-XYLENE, are very unreactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.
Health Hazard
TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
Fire Hazard
Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.
Check Digit Verification of cas no
The CAS Registry Mumber 877-08-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 877-08:
(5*8)+(4*7)+(3*7)+(2*0)+(1*8)=97
97 % 10 = 7
So 877-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6Cl4/c1-3-4(2)6(10)8(12)7(11)5(3)9/h1-2H3
877-08-7Relevant articles and documents
Diversity oriented approach to polycyclic compounds through the diels-alder reaction and the Suzuki coupling
Kotha, Sambasivarao,Misra, Shilpi,Srinivas, Venu
scheme or table, p. 4052 - 4062 (2012/09/07)
A diversity oriented strategy has been demonstrated to deliver small "drug like" molecules using alkylation, Diels-Alder reaction, and Suzuki-Miyaura cross-coupling as key steps. This methodology allows access a wide range of molecules using simple scaffolds such as indanes, tetralins and tetrahydroisoquinolines, which can enhance the chemical space for potential therapeutic molecules.
Studies on the Chemistry of Isoindoles and Isoindolenines, XXXI. 4,5,6,7-Tetrachloro-and 4,5,6,7-Tetrabromo-2H-isoindoles
Kreher, Richard P.,Herd, Karl Josef
, p. 1827 - 1832 (2007/10/02)
The crystalline 2H-isoindoles 4b are synthesized starting with substituted 2-methylsulfonyl-2,3-dihydro-1H-isoindoles 3 by base-induced elimination of methanesulfinic acid.Compared with the parent compound, a considerable thermal stabilization and chemical deactivation is caused by the halogen atoms at the carbocyclic system.The spectroscopic properties of the o-quinonoid hetarenes 4b have been investigated.