CAS: 38411-22-2; 2,2',3,3',6,6'-Hexachlorobiphenyl

该化合物是一种以高热稳定性和绝缘性而闻名的氯化联苯衍生物,该化合物在恶劣的环境条件下极能耐降解,适合各种工业用途,其低挥发性和稳定结构有助于其长期可靠性和持久性.

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2,2',6,6'-tetrachlorobiphenyl 1,2,4-trichloro-3-iodobenzene 2,4,6-trichloro-3-iodoanisole 1,2,4-trichloro-3-iodo-5,6-dimethoxybenzene 1,2,8,9-Tetrachlorodibenzofuran 1,2,6,9-tetrachlorodibenzofuran 1,4,6,9-tetrachlorodibenzofuran biphenyl

合成工艺路线路线简述

    📜4-碘藜芦醚置于盐酸,双氧水,铜体系中,用 氯仿 用作溶剂,化学反应 182.0H,反应生成2,2',3,3',6,6'-六氯联苯
    参考文献:2,2',3,3',6,6'-Hexachlorobiphenyl Hydroxylation By Active Site Mutants Of Cytochrome P450 2B1 And 2B11
    标题:2,2',3,3',6,6'-Hexachlorobiphenyl Hydroxylation By Active Site Mutants Of Cytochrome P450 2B1 And 2B11
    摘要:The Structural Basis Of Species Differences In Cytochrome P450 2B-Mediated Hydroxylation Of 2,2',3,3',6,6'-Hexachlorobiphenyl (236Hcb) Was Evaluated By Using 14 Site-Directed Mutants Of Cytochrome P450 2B1 And Three Point Mutants Of 2B11 Expressed In Escherichia Coli,To Facilitate Metabolite Identification,Seven Possible Products,Including Three Hydroxylated And Four Dihydroxylated Hexachlorobiphenyls,Were Synthesized By Direct Functionalization Of Precursors And Ullmann And Crossed Ullmann Reactions,HPLC And Gc/ms Analysis And Comparison With Authentic Standards Revealed That 2B1 2B11,And All Their Mutants Produced 4,5-Dihydroxy-236Hcb And 5-Hydroxy-236Hcb,While 2B11 L363V And 2B1 I114V Mutants Also Catalyzed Hydroxylation At The 4-Position. The Amount Of Products Formed By 2B1 Mutants I114V,F206L,L209A,T302S,V363A,V363L,V367A,I477A,I477L,G478S,I480A,And I480L Was Smaller Than That Of The Wild Type. I477V Exhibited Unaltered 236Hcb Metabolism,And I480V Produced Twice As Much Dihydroxy Product As The Wild Type,For 2B11,Substitution Of Val-114 Or Asp-290 With Lie Decreased The Product Yields. Replacement Of Leu-363 With Val Dramatically Altered The Profile Of 236Hcb Metabolites. In Addition To An Increase In The Overall Level Of Hydroxylation,The Mutant Mainly Catalyzed Hydroxylation At The 4-Position. Incubation Of P450 2B1 With 5-Hydroxy-236Hcb Produced 4,5-Dihydroxy-236Hcb,Which Indicates That 4,5-Dihydroxy-236Hcb May Be Formed By A Direct Hydroxylation Of 5-Hydroxy-236Hcb. The Findings From This Study Demonstrate The Importance Of Residues 114,206,209,302,363,367,477,478,And 480 In 2B1 And 114,290,And 363 In 2B11 For 236Hcb Metabolism.
    Doi:10.1021/tx990030J

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    合成参考文献


    摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
    参考文献:10.1897/07-359r.1
    摘要:Kania-Korwel I, Hornbuckle KC, Robertson LW, Lehmler HJ. Dose-dependent enantiomeric enrichment of 2,2',3,3',6,6'-hexachlorobiphenyl in female mice. Environ Toxicol Chem. 2008 Feb;27(2):299–305. doi: 10.1897/07-359r.1.
    参考文献:10.1007/s001289900018
    摘要:Christiansen R, Palmork KH. Distribution and Elimination of [14C] in Saithe (Pollachius virens L.) after Application of a Single Dose of [14C] Polyhexamethylene Hydrochloridebiguanide. Bulletin of Environmental Contamination and Toxicology. 1996 Jan;56(1):121–8. doi: 10.1007/s001289900018.
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