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| 4,4'-Dichlorobenzophenone Basic information |
| 4,4'-Dichlorobenzophenone Chemical Properties |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 22-24/25-36-26 | WGK Germany | 3 | RTECS | DJ0525000 | Hazard Note | Irritant | TSCA | Yes | HS Code | 29147000 |
| 4,4'-Dichlorobenzophenone Usage And Synthesis |
Chemical Properties | faintly yellow crystalline powder | Uses | 4,4'-Dichlorobenzophenone is used as pharmaceutical intermediates. It is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and dyestuffs. Bisaminonitrile was polymerized with 4,4'-dichlorobenzophenone using NaH as base. | Preparation | 4,4'-Dichlorobenzophenone is prepared by the acylation of chlorobenzene with 4-chlorobenzoyl chloride. The conversion is typically conducted in the presence of an aluminium chloride catalyst in a petroleum ether solvent. ClC6H5C(O)Cl + C6H5Cl → (ClC6H4)2CO + HCl | Definition | ChEBI: 4-4-Dichlorobenzophenone is a member of benzophenones. | Application | 4,4'-Dichlorobenzophenone can be used to synthesize polyether-polyketones, as well as reduce polymer costs. Furthermore, it is a metabolic product resulting from the degredation of DDT. | Synthesis Reference(s) | The Journal of Organic Chemistry, 54, p. 1201, 1989 DOI: 10.1021/jo00266a039 Tetrahedron Letters, 36, p. 8411, 1995 DOI: 10.1016/0040-4039(95)01802-O | General Description | 4,4′-Dichlorobenzophenone (DBP) is a metabolite obtained when one strain of ectomycorrhizal fungi, Xerocomus chrysenteron, degrades 1,1,1-trichloro-2,2-bis(4-chlorophe-nyl) ethane (DDT). | Purification Methods | Recrystallise it from EtOH [Wagner et al. J Am Chem Soc 108 7727 1986]. The semicarbazone has m 192-193o (from H2O). [Beilstein 7 H 420, 7 I 228, 7 II 359, 7 III 2076, 7 IV 1376.] |
| 4,4'-Dichlorobenzophenone Preparation Products And Raw materials |
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