CAS: 1022-46-4; Bentranil

该化合物是一个环环环有机化合物,其特点是苯氧基结构,具有苯丙胺和氧化氮环.该化合物一般在室温中处于固态,以其在包括制药和材料科学在内的各个领域的潜在应用而著称.它拥有一个有助于其芳香特性的苯基组,增强了其稳定性和再活性.氧化氮混合物的存在会影响其化学行为,使其成为合成有机化学的一个对象.此外,该化合物可能表现出荧光性,这在某些分析应用中可能有用.其溶性因溶剂不同而不同,它可能参与各种化学反应,包括电益替代和环状.

结构式图片

相似化合物

18600-54-9 117039-85-7 18600-53-8

物理性质

MSDS等安全信息

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号98-88-4 苯甲酰氯 | CAS号118-92-3 邻氨基苯甲酸 | CAS号948-65-2 2-苯基吲哚 | CAS号201230-82-2 carbon monoxide | CAS号615-43-0 2-碘苯胺 | CAS号31588-18-8 3-羟基-2-苯基喹啉-4(1H)-酮 | CAS号579-93-1 2-(苯甲酰基氨基)苯甲酸 | CAS号326903-42-8 2-benzoylamino-... | CAS号70787-27-8 N-(2-bromopheny... | CAS号118-48-9 靛红酸酐 | CAS号6484-25-9 4-氯-2-苯基喹唑啉 | CAS号579-93-1 2-(苯甲酰基氨基)苯甲酸 | CAS号30909-95-6 5H-1,3,4-Benzot... | CAS号1022-45-3 2-苯基-4-[3H]喹唑啉酮 | CAS号148321-04-4 4-(4-oxo-2-phen... | CAS号17240-30-1 9-phenyl-8-thia... | CAS号123845-83-0 3-[2-(4-oxo-2-p... | CAS号1904-60-5 3-氨基-2-苯基-4(3H)-喹唑啉酮 | CAS号18543-23-2 2-benzamido-N-p... | CAS号100-52-7 苯甲醛

合成工艺路线路线简述

  • 合成目标产物 Bentranil 主要起始原料 2-Iodobenzoic Acid And Benzonitrile
  • (文献来源)合成步骤主要原料 2-Iodobenzoic Acid 和 Benzonitrile
📜邻苯甲酰苯甲酸置于sodium Azide,氯仿,硫酸,三氯乙酸体系中,化学反应生成苯草灭
参考文献:743. Schmidt与邻苯甲酰基苯甲酸反应的机理
标题:743. Schmidt与邻苯甲酰基苯甲酸反应的机理
摘要:
Doi:10.1039/jr9530003698

专利信息


专利号:US-2004030209-A1
优先权日:2000-11-30
标 题:Method for the production of alkyl aryl sulphonates
发明人：NARBESHUBER THOMAS; STEINBRENNER ULRICH; KRACK GERHARD
摘要:The preparation of alkylaryl compounds takes place by n 1) preparation of a mixture of, on statistical average, predominantly monobranched C 10-14 -olefins by n a) reaction of a C 4 -olefin mixture over a metathesis catalyst for the preparation of an olefin mixture comprising 2-pentene and/or 3-hexene, and optional removal of 2-pentene and/or 3-hexene, followed by dimerization of the resulting 2-pentene and/or 3-hexene over a dimerization catalyst to give a mixture comprising C 10-12 -olefins, and optionally removal of the C 10-12 -olefins, or n b) extraction of predominantly monobranched paraffins from kerosene cuts and subsequent dehydrogenation, or n c) Fischer-Tropsch synthesis of olefins or paraffins, where the paraffins are dehydrogenated, or n d) dimerization of shorter-chain internal olefins, or n e) isomerization of linear olefins or paraffins, where the isomerized paraffins are dehydrogenated, n 2) reaction of the olefin mixture obtained in stage 1) with an aromatic hydrocarbon in the presence of an alkylation catalyst which contains zeolites of the faujasite type.

专利号:CN-104761558-B
优先权日:2015-04-10
标题 :A kind of one-pot synthesis method of quinazolinone and indazole derivatives

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主要参考文献


1: Miccio-Fonseca LC. MEGA♪ Tool: An Analysis of "Risk/Treatment Needs and Progress Protocol" by Kang, Beltrani, Manheim, Spriggs, Nishimura, Sinclair, Stachniuk, Pate, Righthand, Prentky, and Worling (2019). J Child Sex Abus. 2020 Apr;29(3):351-372. doi: 10.1080/10538712.2020.1733161. Epub 2020 Mar 5. 9(2):1. 1(4):380-8. doi: 10.1007/s11882-001-0052-0. 83(6 Pt 2):607-13. doi: 10.1016/S1081-1206(10)62881-5. 3887(3):251-97. doi: 10.11646/zootaxa.3887.3.1. 78(2):160-73; quiz 174-6. doi: 10.1016/S1081-1206(10)63383-2. 3(2):115-23. doi: 10.1097/00130832-200304000-00005. 14(1):171-198. doi: 10.1016/s0733-8635(05)70338-7. 11(3):171-6, 179-85; quiz 186-7. 10(12):e0144167. doi: 10.1371/journal.pone.0144167.
11: Faraj Y, Beltrani VP. Introduction to Head and Neck Melanoma: A Dermatologist's Perspective. Oral Maxillofac Surg Clin North Am. 2022 May;34(2):213-220. doi: 10.1016/j.coms.2021.11.007.
207:105492. doi: 10.1016/j.actatropica.2020.105492. Epub 2020 Apr 13. 16(7):e0253599. doi: 10.1371/journal.pone.0253599.

合成参考文献


摘要:Camp, J. E., Science of Synthesis Knowledge Updates, (2012) 1, 314.
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