CAS: 2008-58-4; 2,6-Dichlorobenzamide

该化合物是一种有机化合物,其特点是芳香结构,其特点是2和6个位置上用两个氯原子替换的苯环,以及一个氨化功能组,其分子分子式为C7H5Cl2N,其分子重量反映这些元素的存在.该化合物一般是白色的,在标准条件下以其稳定性为名,在有机溶剂中溶解,但在水中溶解性有限. 2,6-二氯苯并胺主要用于农业用途,特别是作为除草剂,因为它能够抑制某些植物生长过程.此外,它可能在研究环境中,特别是在与植物生理学和生物化学有关的研究中,应用.安全数据表明,与许多氯化化合物一样,应谨慎处理该化合物,以避免潜在的环境和健康风险.适当的储存和处置方法对于减轻与使用该化合物相关的任何不利影响至关重要.

结构式图片

上下游产品

CAS号25185-95-9 2,6-二氯苯甲醛肟 | CAS号1194-65-6 2,6-二氯苯腈 | CAS号83-38-5 2,6-二氯苯甲醛 | CAS号19393-92-1 1-溴-2,6-二氯苯 | CAS号3019-71-4 三氯乙酰基异氰酸酯 | CAS号144-55-8 碳酸氢钠 | CAS号4659-45-4 2,6-二氯苯甲酰氯 | CAS号6575-28-6 (E)-2,6-dichlor... | CAS号3714-77-0 (Z)-2,6-DICHLOR... | CAS号118-69-4 2,6-二氯甲苯 | CAS号608-31-1 2,6-二氯苯胺 | CAS号35377-49-2 2,6-dichloroben... | CAS号35409-97-3 除幼脲 | CAS号35367-09-0 2,6-dichloro-N-... | CAS号1194-65-6 2,6-二氯苯腈 | CAS号116800-83-0 METHYL N-(2,6-D... | CAS号67048-91-3 5-(2,6-dichloro... | CAS号92207-23-3 2,6-dichloro-N-...

合成工艺路线路线简述

    2,6-二氯苯甲酰氯置于ammonium Hydroxide体系中,用 二氯甲烷 用作溶剂,化学反应 3.5H,反应生成2,6-二氯苯甲酰胺
    参考文献:含有酰肼-Hydr和羧酰胺基团的新型1,3-噻唑衍生物的合成,抗肿瘤活性和作用机理
    标题:含有酰肼-Hydr和羧酰胺基团的新型1,3-噻唑衍生物的合成,抗肿瘤活性和作用机理
    摘要:合成了一系列新颖的2,4,5-三取代1,3,3-噻唑衍生物,其中包括酰肼-肼,以及包括46个化合物t的羧酰胺部分,并评估了它们在体外对五种人类癌细胞系的抗肿瘤活性.18种标题化合物t对mcf-7,Hepg2,Bgc-823,Hela和a549细胞系的抑制活性高于5-Fu.尤其是,T1,T26和t38表现出最佳的ic 50细胞毒性活性分别针对mcf-7,Bcg-823和hepg2细胞系的2.21μg/ Ml,1.67μg/ Ml和1.11μg/ Ml值.这些结果表明,1,3-噻唑,酰肼-Hydr和羧酰胺部分的组合对细胞毒性活性非常有利.此外,流式细胞仪分析表明,化合物t1和t38可以诱导hepg2细胞凋亡,并证实t38通过s细胞周期停滞诱导了细胞凋亡的诱导.
    Doi:10.1016/j.Bmcl.2016.05.059

    海关参考信息

    专利信息


    专利号:CN-102477452-A
    优先权日:2010-11-22
    标题:Enzymatic Synthesis of a Surfactant

    专利号:US-5354905-A
    优先权日:1992-10-23
    标 题 :N-alkoxymethyl benzamide derivative and manufacturing method therefor, and manufacturing method for benzamide derivative using this N-alkoxymethyl benzamide derivative
    发明人:SATO YOSHIHIRO; KOISO AKIHIRO; ASADA TOHRU; MIURA YASUHISA; KIKUCHI YASUO; HARIYA YASUAKI
    权利人:YASHIMA KAGAKU KOGYO KK
    摘要:An N-alkoxymethyl benzamide derivative represented by Formula (I); (I) (In the formula, reference X indicates a halogen atom, references Y1 and Y2 indicate hydrogen atoms or halogen atoms, and may be identical or different, and reference R indicates a lower alkyl group.) and a manufacturing method for this N-alkoxymethyl benzamide derivative in which a substituted benzamide and an alpha -haloacetal are reacted. Furthermore, a manufacturing method for benzamide derivatives in which the N-alkoxymethyl benzamide derivative represented by Formula (I) above and benzene or a derivative thereof are reacted, and a benzamide derivative is produced. The N-alkoxymethyl benzamide derivative of the present invention is a novel compound, and possesses utility as an intermediate in the manufacturing of oxazoline derivatives which possess insecticidal and anti-mite activity, and as a starting material for the synthesis of various organic compounds and the like.

    专利号:US-5096710-A
    优先权日:1989-05-27
    标 题 :Poison bait for control of noxious insects
    发明人:MINAGAWA FUMIYASU; KOHAMA TAKUJI; KAWADA HITOSHI; SHINJO GORO; MAEDA KAZUYUKI
    权利人:SUMITOMO CHEMICAL CO
    摘要:A bait composition in a tablet form, which comprises as the essential components (a) at least one insect-growth controlling agent chosen from (a-1) insect juvenile hormone-like compounds and (a-2) insect chitin-synthesis inhibitors, (b) dextrin and (c) a plant oil in an amount of not more than 10% by weight to the total bait composition.

    专利号:US-9701686-B2
    优先权日:2009-12-04
    标题:Tricyclopyrazole derivatives
    发明人:DISINGRINI TERESA; MANTEGANI SERGIO; VARASI MARIO
    权利人:NERVIANO MEDICAL SCIENCES SRL
    摘要:Compounds which are tricyclopyrazole derivatives or pharmaceutically acceptable salts thereof, their preparation process and pharmaceutical compositions comprising them are disclosed; these compounds are useful in the treatment of diseases caused by and/or associated with an altered protein kinase activity such as cancer, viral infection, prevention of AIDS development in HIV-infected individuals, cell proliferative disorders, autoimmune and neurodegenerative disorders; also disclosed is a process under Solid Phase Synthesis conditions for preparing the compounds of the invention and chemical libraries comprising a plurality of them.
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    合成参考文献


    摘要:Asano, Y., Science of Synthesis: Biocatalysis in Organic Synthesis, (2015) 1, 258.
    摘要:Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-159
    摘要:Currance, P.L. Clements, B., Bronstein, A.C. (Eds).; Emergency Care For Hazardous Materials Exposure. 3rd revised edition, Elsevier Mosby, St. Louis, MO 2007, p. 176-7
    摘要:Fournier JC, Salle J; Chemosphere 3: 77-82 (1974)
    摘要:Holtze MS et al; Environ Pollut 148: 343-351 (2007)
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