CAS: 112225-87-3; N'-Benzoyl-N-(Tert-Butyl)Benzohydrazide

该化合物是一种有机化合物,其特征是氢氮功能组,代之以两个苯并基组和一个叔丁基组,该化合物一般在室温时是固体,在正常条件下以其稳定性著称,经常用于有机合成,并可作为各种化学产品生产的前体或中间体,苯并基组的存在有助于其再活动,特别是在电光替代反应中.此外,三丁基组会增强氢氨基物质周围的阻塞性,有可能影响其再活性和有机溶剂中的溶解性.该化合物可能具有令人感兴趣的特性,如荧光或光化学活动,使其对材料科学和光化学化学具有兴趣.在处理和储存时,应参考安全数据,如任何化学物质,以确保对与氢氨及其衍生物有关的潜在危害采取适当的防范措施.

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CAS号7400-27-3 叔丁基肼盐酸盐 | CAS号98-88-4 苯甲酰氯 | CAS号17473-79-9 Benzoic acid,2-... | CAS号32154-73-7 Hydrazine, (1,1... | CAS号65715-09-5 phenyl-(5-pheny... | CAS号57064-92-3 3-benzoyl-5-phe...

合成工艺路线路线简述

    叔丁基肼盐酸盐,苯甲酰氯置于n,N-二异丙基乙胺体系中,用 二氯甲烷 用作溶剂,以86 %的收率获得n-苯甲酰基-N'-特丁基苯甲酰肼
    参考文献:了解 N,N'-二酰肼的顺式-反式酰胺键异构化,以制定先验预测其最稳定溶液构象异构体的指南
    标题:了解 N,N'-二酰肼的顺式-反式酰胺键异构化,以制定先验预测其最稳定溶液构象异构体的指南
    摘要:N,N '-二酰肼(r 1 Co-Nr 3-Nr 4-Cor 2 )是一类在化学和生物学领域具有广泛应用的小分子.它们在结构上是独特的,因为它们的两个酰胺基团通过 N-N 单键连接,因此,这些分子可以以八种不同的异构形式存在.其中四种是由 C-N 键产生的酰胺异构体 [反式-反式 (T-T),反式-顺式 (T-C),顺式-反式 (C-T) 和顺式-顺式 (C-C)]限制旋转.此外,由于n-N键限制旋转,这些酰胺异构体中的每一种都可以以两种不同的异构体形式存在,特别是当r 3和r 4基团相对较大时.在此,我们结合溶液核磁共振波谱,X射线晶体学和密度泛函理论计算,系统地研究了 55 N,N'-二酰基肼的构象.我们的数据表明,当氮原子上的取代基r 3和r 4都是氢时.这些分子更喜欢扭曲的反式-反式 (T-T) (>90%) 几何形状 (H-N-C=o ∼ 180°),而n-烷基化和n
    Doi:10.1021/acs.Joc.2C01891

    海关参考信息

    专利信息


    专利号:US-5110986-A
    优先权日:1988-04-26
    标题:Synthesis of n-t-alkyl-1,2-diacylhydrazines
    发明人:KELLY MARTHA J
    权利人:ROHM & HAAS
    摘要:A process for preparing a N-t-alkyl-1,2-diacylhydrazine comprises reacting a 1, 3, 4-oxadiazole with a tertiary alkyl cation precursor in the presence of a strong acid catalyst.

    专利号:US-8293797-B2
    优先权日:2004-02-19
    标题:Use of molt-accelerating compounds, ecdysteroids, analogs thereof, and chitin synthesis inhibitors for controlling termites
    发明人:SU NAN-YAO; KING JAMES EDWARD; NEESE PAUL ALLEN
    权利人:SU NAN-YAO; KING JAMES EDWARD; NEESE PAUL ALLEN; UNIV FLORIDA
    摘要:The subject invention relates in part to the oral administration of ecdysteroids for controlling subterranean termites. Preferred ecdysteroids for use according to the subject invention are ecdysone, certain ecdysone analogs, and 20-hydroxyecdysone, for example. In some preferred embodiments, one or more of these compounds is used in a termite bait in combination with one or more chitin synthesis inhibitors. Thus, the subject invention also relates in part to controlling termites by the use of a chitin synthesis inhibitor (CSI), such as hexaflumuron and/or noviflumuron, together with an ecdysteroid (and analogs thereof) or molt-accelerating compound (MAC), such as halofenozide. The subject invention also relates to mixtures comprising these two active ingredients. The MAC/ecdysteroid analog induces a preliminary molting event in termite workers (they could not complete the molting), which then allows the CSI to further disrupt the molt and cause mortality. The combination of these active ingredients, causing accelerated molting together with inhibition of chitin synthesis, is surprisingly shown herein to enhance activity against termites, as compared to either group of compounds alone.

    专利号:EP-0339854-B1
    优先权日:1988-04-26
    标 题 :Synthesis of n-t-alkyl-1,2-diacylhydrazines

    专利号:CN-1038277-A
    优先权日:1988-04-26
    标题:Synthesis of N-tert-alkyl-1,2-diacylhydrazines

    专利号:EP-0339854-A2
    优先权日:1988-04-26
    标题 :Synthesis of N-t-alkyl-1,2-diacylhydrazines

    专利号:US-2008242647-A1
    优先权日:2004-02-19
    标 题 :Use of Molt-Accelerating Compounds, Ecdysteroids, Analogs Thereof, and Chitin Synthesis Inhibitors for Controlling Termites
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    主要参考文献


    1: Clements JS 2nd, Islam R, Sun B, Tong F, Gross AD, Bloomquist JR, Carlier PR. N'-mono- and N, N'-diacyl derivatives of benzyl and arylhydrazines as contact insecticides against adult Anopheles gambiae. Pestic Biochem Physiol. 2017 Nov;143:33-38. doi: 10.1016/j.pestbp.2017.10.001. Epub 2017 Oct 7. doi: 10.1002/bmc.3732. Epub 2016 Apr 26. doi: 10.1016/j.bmcl.2016.01.047. Epub 2016 Jan 18. doi: 10.1002/ps.3353. Epub 2012 Jul 3. doi: 10.1002/ps.3350. Epub 2012 Jun 22. doi: 10.1002/ps.3274. Epub 2012 Mar 29. doi: 10.1007/s00216-011-5699-3. Epub 2012 Jan 20. doi: 10.3233/JAD-2011-111238. Chinese. doi: 10.1016/j.steroids.2010.09.009. Epub 2010 Oct 27. doi: 10.1016/j.cbpb.2010.04.017. Epub 2010 May 6. Epub 2007 Sep 14. Epub 2006 Aug 23.

    合成参考文献


    参考文献:10.1042/bst024438s
    摘要:Williams DR, Chen JH, Fisher MJ, Rees HH. Ecdysteroid inactivation in response to elevated levels of 20-hydroxyecdysone or an agonist, RH 5849 in the tobacco hornworm, Manduca sexta. Biochem Soc Trans. 1996 Aug;24(3):438S. doi: 10.1042/bst024438s.
    参考文献:10.1016/s0014-5793(96)01413-5
    摘要:Löw P, Bussell K, Dawson SP, Billett MA, Mayer RJ, Reynolds SE. Expression of a 26S proteasome ATPase subunit, MS73, in muscles that undergo developmentally programmed cell death, and its control by ecdysteroid hormones in the insect Manduca sexta. FEBS Lett. 1997 Jan 06;400(3):345–9. doi: 10.1016/s0014-5793(96)01413-5.
    参考文献:10.1016/s0965-1748(99)00077-6
    摘要:Farkas R, Sláma K. Effect of bisacylhydrazine ecdysteroid mimics (RH-5849 and RH-5992) on chromosomal puffing, imaginal disc proliferation and pupariation in larvae of Drosophila melanogaster. Insect Biochem Mol Biol. 1999 Nov;29(11):1015–27. doi: 10.1016/s0965-1748(99)00077-6.
    参考文献:10.1021/jf800740z
    摘要:Zhao Q, Shang J, Huang Z, Wang K, Bi F, Huang R, Wang Q. Synthesis and Insecticidal Activities of Novel N-Sulfenyl-N′-tert-butyl-N,N′-diacylhydrazines. 2. N-Substituted Phenoxysulfenate Derivatives. J. Agric. Food Chem. 2008 Jun 10;56(13):5254–9. doi: 10.1021/jf800740z.
    参考文献:10.1021/jf9043277
    摘要:Li Y, Li BJ, Ling Y, Miao HJ, Shi YX, Yang XL. Synthesis and fungicidal activity of aryl carbamic acid-5-aryl-2-furanmethyl ester. J Agric Food Chem. 2010 Mar 10;58(5):3037–42. doi: 10.1021/jf9043277.
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