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1,4-Dichlorobenzene (1,4-DCB, p-DCB, or para-dichlorobenzene, sometimes abbreviated as PDCB or para) is an aryl chloride and isomer of dichlorobenzene with the formula C 6 H 4 Cl 2. This colorless solid has a strong odor. The molecule consists of a benzene ring with two chlorine atoms (replacing hydrogen atoms) on opposing sites of the ring.
1,2-Dichlorobenzene or ortho-dichlorobenzene; 1,3-Dichlorobenzene or meta-dichlorobenzene; 1,4-Dichlorobenzene or para-dichlorobenzene. All three isomers are colorless chlorobenzenes with the formula C 6 H 4 Cl 2. They differ structurally based on where the two chlorine atoms are attached to the ring.
1,4-Dicyanobenzene is an organic compound with the formula C 6 H 4 (CN) 2. Two other isomers exist, phthalonitrile and isophthalonitrile. All three isomers are produced commercially by ammoxidation of the corresponding xylene isomers. 1,4-Dicyanobenzene is a colorless or white solid with low solubility in water. [1]
633.4 K (360.25°C), 4.52 MPa Std enthalpy change of fusion, Δ fus H o? kJ/mol Std entropy change of fusion, Δ fus S o: 9.6 J/(mol·K) Std enthalpy change of vaporization, Δ vap H o: 40.97 kJ/mol Std entropy change of vaporization, Δ vap S o? J/(mol·K) Solid properties Std enthalpy change of formation, Δ f H o solid? kJ/mol Standard molar ...
Older mothballs consisted primarily of naphthalene, but due to naphthalene's flammability, many modern mothball formulations instead use 1,4-dichlorobenzene. The latter formulation may be somewhat less flammable, although both chemicals have the same NFPA 704 rating for flammability. The latter chemical is also variously labeled as para ...
Disperse Yellow 42, a popular dye for polyesters, is derived from 1,4-dichloro-2-nitrobenzene. [1] 1,4-Dichloro-2-nitrobenzene is an organic compound with the formula C 6 H 3 Cl 2 NO 2. One of several isomers of dichloronitrobenzene, it is a yellow solid that is insoluble in water. It is produced by nitration of 1,4-dichlorobenzene. It is a ...
They have the formula C 6 H 6–n Cl n, where n = 1–6 is the number of chlorine atoms. Depending on the number of chlorine substituents, there may be several constitutional isomers possible. Monochlorobenzene; Dichlorobenzene. 1,2-Dichlorobenzene; 1,3-Dichlorobenzene; 1,4-Dichlorobenzene; Trichlorobenzene. 1,2,3-Trichlorobenzene; 1,2,4 ...
When quenched by tetrachloromethane the reaction product is a 1,4-dichlorobenzene and with methanol the reaction product is benzyl alcohol. When the enyne moiety is incorporated into a 10-membered hydrocarbon ring (e.g. cyclodeca-3-ene-1,5-diyne in scheme 2 ) the reaction, taking advantage of increased ring strain in the reactant, is possible ...