CAS: 1079-21-6; [1,1'-Biphenyl]-2,5-Diol

该化合物其结构特征为:苯球类和苯环上的两个氢氧基组,其表面是白色的黄色晶状固体,可溶于水,酒精和乙醚,其抗氧化特性为人所知,在包括化妆品和食品保存在内的各种应用中有用,有助于防止氧化性降解;苯丙酮也可以作为化学反应的减少剂;其稳定性和再活性受氢氧类的存在影响,这些组可参与氢结合并影响其溶性以及与其他物质的相互作用;此外,必须谨慎处理这种化合物,因为如果浸入或吸入,可能会对健康造成危害,在实验室或工业环境中使用时,应采取适当的安全措施.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

邻苯基苯酚 2-Phenylphenol 90-43-7
间羟基联苯 3-Phenylphenol 580-51-8
O-(2-Biphenylyl)Hydroxylamine 107449-13-8
苯基对苯二酚二乙酯 2,5-Diacetoxybiphenyl 58244-28-3

合成工艺路线路线简述

    📜苯基-P-苯醌置于cp*ir(6,6'-Dionato-2,2'-Bipyridine)(H2O),氢气体系中,用 2-甲基-2-丁醇 用作溶剂,以91 %的收率获得2,5-二羟基联苯
    参考文献:金属配体双功能铱催化剂催化醌在大气压下氢化成对苯二酚
    标题:金属配体双功能铱催化剂催化醌在大气压下氢化成对苯二酚
    摘要:已经开发出在大气压下将醌氢化为氢醌的通用方法.在 [cp*ir(2,2'-Bpyo)(H 2 O)] (0.5-1 Mol %) 存在下,以高产率获得了一系列产品.此外,还将该催化体系扩展到1,4-苯醌二亚胺的氢化反应.人们发现 Bpy 配体中的官能团对于铱配合物的催化活性至关重要.
    Doi:10.1021/acs.Orglett.4C00064

    海关参考信息

    专利信息


    专利号:US-5146008-A
    优先权日:1988-06-16
    标 题:Process for the synthesis of aromatic phenyl substituted diols
    发明人:GARDANO ANDREA; COASSOLO ALFREDO; CASAGRANDE FRANCESCO; FOA MARCO; CHAPOY LARRY L
    权利人:HIMONT ITALIA
    摘要:A process for the synthesis of phenyl substituted aromatic diols, obtained by dehydrogenation of the corresponding substituted cyclohexyl derivatives in the presence of a palladium supported catalyst, said palladium supported catalyst being prepared by a process which comprises treating a palladium hydrolysis compound with reducing agents.

    专利号:US-7147800-B2
    优先权日:2001-01-23
    标题 :Selective ether cleavage synthesis of liquid crystals
    发明人:WELLINGHOFF STEPHEN T; HANSON DOUGLAS P
    权利人:SOUTHWEST RES INST
    摘要:A method for making platform molecules comprising: reacting 4-alkoxy benzoyl chloride with R2-hydroquinone under first conditions effective to produce bis 1,4[4-alkoxy-benzoyloxy]-R2-phenylene comprising bis terminal alkoxy groups wherein R2 is a bulky organic group; and, subjecting the bis 1,4[4-alkoxy-benzoyloxy]-R2-phenylene to second conditions effective to selectively cleave the bis terminal alkoxy groups to produce a solution comprising complexes comprising diphenolic platform molecules comprising bis terminal hydroxyl groups, the second conditions also being effective to precipitate the complexes out of the solution.

    专利号:US-5098531-A
    优先权日:1988-03-24
    标题 :Electrochemical synthesis of 2-aryl-hydroquinones
    发明人:GATTI NORBERTO; FOA MARCO
    权利人:DONEGANI GUIDO IST
    摘要:Preparation of 2-aryl-hydroquinones of formula (I) by oxidizing by an electrochemical route a compound of formula (II): ##STR1## wherein A represents an aryl group optionally substituted with groups compatible with the reaction conditions in an acidic aqueous reaction medium, at temperatures within the range of from 10° to 100° C., and with anodes of graphite or PbO 2 . The products are used in photography and in the field of liquid-crystal polymers.

    专利号:US-4847429-A
    优先权日:1987-08-03
    标 题:Synthesis of phenylhydroquinones
    发明人:LENTZ CARL M; GUSTAFSON BRUCE L; VAN SICKLE DALE E; BOWERS JR JOSEPH S
    权利人:EASTMAN KODAK CO
    摘要:Process is disclosed for the preparation of phenylhydroquinones by the alkylation of hydroquinone (or derivatives thereof) with the cyclohexyl moieties, cyclohexanol or cyclohexene (or derivatives thereof), followed by dehydrogenation of the intermediate cyclohexylhydroquinone.

    专利号:US-2004144954-A1
    优先权日:2001-01-23
    标 题 :Selective ether cleavage synthesis of liquid crystals

    专利号:US-2003055280-A1
    优先权日:2001-01-23
    标 题:Methods for synthesis of liquid crystals

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Nakata Y, Nishi K, Nishimoto S, Sugahara T. Phenylhydroquinone induces loss of thymocytes through cell cycle arrest and apoptosis elevation in p53-dependent pathway. J Toxicol Sci. 2013;38(3):325-35.

    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:10.1007/s002040050318
    摘要:Guhe C, Degen GH, Schuhmacher US, Kiefer F, Föllmann W. Drug metabolizing enzyme activities in porcine urinary bladder epithelial cell cultures (PUBEC). Archives of Toxicology. 1996 Aug 01;70(10):599–606. doi: 10.1007/s002040050318.
    参考文献:10.1093/carcin/13.8.1469
    摘要:Ushiyama K, Nagai F, Nakagawa A, Kano I. DNA adduct formation by O-phenylphenol metabolite in vivo and in vitro. Carcinogenesis. 1992;13(8):1469–73. doi: 10.1093/carcin/13.8.1469.
    参考文献:10.1016/0165-7992(94)90056-6
    摘要:Tayama S, Nakagawa Y. Effect of scavengers of active oxygen species on cell damage caused in CHO-K1 cells by phenylhydroquinone, an o-phenylphenol metabolite. Mutation Research Letters. 1994 Jul;324(3):121–31. doi: 10.1016/0165-7992(94)90056-6.
    参考文献:10.1016/0165-1218(94)90100-7
    摘要:Christine Lambert A, Eastmond DA. Genotoxic effects of the o-phenylphenol metabolites phenylhydroquinone and phenylbenzoquinone in V79 cells. Mutation Research/Genetic Toxicology. 1994 Oct;322(4):243–56. doi: 10.1016/0165-1218(94)90100-7.
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