CAS: 3698-83-7; 1,5-Dichloro-2,4-Dinitrobenzene

该化合物是一种有机化合物,其特点是芳香结构,有两个氯原子和两个硝基组,附于一个苯环,这些替代成分的存在对其化学特性有重大影响,使其成为一个极极化和反应性很强的化合物,典型的似乎是黄色晶状固体,因其在各种应用中的潜在用途,包括作为染料和药物合成的中间体而闻名;该化合物还因其毒性和环境持久性而得到承认,需要小心处理和处置;其分子结构有助于其在正常条件下的稳定性,但可经受各种化学反应,例如核循环生物替代和减少;由于其危险性质,1,3-二氯-4,6-二硝基苯受到严格的监管,在实验室或工业环境中与该物质打交道时,安全防范是不可或缺的.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

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CAS号541-73-1 间二氯苯 | CAS号50981-12-9 oxidanium,hydro... | CAS号611-06-3 2,4-二氯硝基苯 | CAS号616-74-0 4,6-二硝基间苯二酚 | CAS号554-00-7 2,4-二氯苯胺 | CAS号121-73-3 间氯硝基苯 | CAS号108-43-0 3-氯酚 | CAS号54715-57-0 3-CHLORO-4,6-DI... | CAS号98-59-9 对甲苯磺酰氯(PTSC) | CAS号50-84-0 2,4-二氯苯甲酸 | CAS号34033-44-8 2,4-二氯-5-硝基-苯基胺 | CAS号51652-35-8 5-甲氧基-2,4-二硝基苯酚 | CAS号327-92-4 1,5-二氟-2,4-二硝基苯 | CAS号20248-64-0 4,6-二氯-1,3-苯二胺 | CAS号2789-24-4 Benzo[1,2-d:5,4... | CAS号616-74-0 4,6-二硝基间苯二酚 | CAS号67073-39-6 4-氯-5-硝基-O-苯二胺 | CAS号327-91-3 Benzene,1-chlor... | CAS号1630-09-7 2,4-二氯-1,3,5-三硝基苯 | CAS号112274-31-4 2,6-diphenyl-1,...

合成工艺路线路线简述

    📜3-硝基氯苯置于氯化亚砜,硫酸,硝酸体系中,化学反应生成1,5-二氯-2,4-二硝基苯
    参考文献:Davies; Hickox,Journal Of The Chemical Society,1922,Vol. 121,P. 2649
    标题:Davies; Hickox,Journal Of The Chemical Society,1922,Vol. 121,P. 2649

    海关参考信息

    专利信息


    专利号:US-2013158296-A1
    优先权日:2009-12-21
    标题:Process for the synthesis of 1-amino-3-halo-4,6-dinitrobenzene
    发明人:HARGIS ANNALISA; RITTER JOACHIM C
    权利人:HARGIS ANNALISA; RITTER JOACHIM C; DU PONT
    摘要:A process is provided for the preparation of 1-amino-3-halo-4,6-dinitrobenzene and related compounds by monoamination of dihalodinitrobenzenes by ammonia in the presence of solvent and water. Using glycol as a solvent for the dihalodinitrobenzene and feeding ammonia at a rate at which it is consumed allows for the synthesis of high purity product, such as 1-amino-3-chloro-4,6-dinitrobenzene, at high yields.

    专利号:US-8071812-B1
    优先权日:2007-12-18
    标题:Process for the synthesis of 1,3-diamino-4,6-dinitrobenzene
    发明人:RITTER JOACHIM C; HARGIS ANNALISA
    权利人:RITTER JOACHIM C; HARGIS ANNALISA; DU PONT
    摘要:A process is provided for the preparation of 1,3-diamino-4,6-dinitrobenzene by amination of 1,3-dihalo-4,6-dinitrobenzene. The presence of water advantageously results in a highly pure product, free or essentially free of glycol ether impurities.

    专利号:US-8003831-B1
    优先权日:2007-12-18
    标 题:Process for the synthesis of dihalodinitrobenzenes
    发明人:RITTER JOACHIM C
    权利人:DU PONT
    摘要:A process is provided for the preparation of 1,3-dihalo-4,6-dinitrobenzene by the nitration of 1,3-dihalobenzene. The direct isolation of highly pure 1,3-dihalo-4,6-dinitrobenzene is accomplished without a water or ice quench, and involves the use of at least one equivalent of SO 3 during the reaction, slow crystallization, and isolation of product from a cold crystal slurry.

    专利号:WO-2011084773-A2
    优先权日:2009-12-21
    标 题 :Process for the synthesis of 1-amino-3-halo-4,6-dinitrobenzene

    专利号:CN-110627738-A
    优先权日:2019-10-23
    标题 :A kind of synthetic method that is used for the synthesis of the pesticide intermediate of flurafen

    专利号:US-5105012-A
    优先权日:1989-03-24
    标题 :Catalytic reduction of dinitrobenzenes using a noble metal catalyst and iron or iron salts
    发明人:THEODORIDIS GEORGE
    权利人:FMC CORP
    摘要:There is provided an improved process for the reduction of optionally substituted dinitrobenzenes to the corresponding nitroanilines with high yields which comprises contacting the dinitrobenzene with hydrogen in an acidic medium in the presence of a catalytic amount of a combination of a noble metal hydrogenation catalyst, and iron or an iron salt. Isomer specific reductions may be achieved with those compounds containing suitable directing substituents. The 2-halo-5-nitroanilines which may be produced in this process may be converted via a multi-step synthesis to useful 1-aryl-4-substituted 1,4-dihydro-5H-tetrazol-5-one herbicides.

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    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

    [参考文献]: Bingjie Qin, Et Al. Diarylaniline Derivatives As A Distinct Class Of Hiv-1 Non-Nucleoside Reverse Transcriptase Inhibitors. J Med Chem. 2010 Jul 8;53(13):4906-16.

    合成参考文献


    摘要:Schafer, E. W., Jr., W. A. Bowles Jr., and J. Hurlbut. 1983. The acute oral toxicity and repellency and hazard potential of 998 chemicals to one or more species of wild and domestic birds. Archives of Environmental Contamination and Toxicology 12:355-382.
    参考文献:10.1007/s10863-006-9034-1
    摘要:Provost E, Shearn A. The Suppressor of Killer of prune, a unique glutathione S-transferase. Journal of Bioenergetics and Biomembranes. 2006 Aug 31;38(3-4):189. doi: 10.1007/s10863-006-9034-1.
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