- 英文名称1-Bromo-2,3,4-Trifluorobenzene
- 中文名称2,3,4-三氟溴苯
- IUPAC名称1-bromo-2,3,4-trifluorobenzene
- 其它别名1-溴-2,3,4-三氟苯; 2,3,4-Trifluorobromobenzene
- CAS编号176317-02-5
- MFCD编号:MFCD00013248
- EINECS号:631-503-9
- 分子式:C6H2BrF3
- 分子量:210.98
- 产品CID: 899150
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
欧盟法规
ECHA物质C&L通报上下游产品
2,3,4-trifluoroaniline 1,2,3-trifluorobenzene 4-methyl-1,2,3-trifluorobenzene 1-bromo-4,5,6-trifluoro-2-[(4-methoxyphenyl)aminosulfonyl]benzene 1-Bromo-2,3,4-trifluoro-5-[(4-methoxyphenyl)aminosulfonyl]benzene 1-iodo-2,3,4-trifluorobenzene 合成工艺路线路线简述
- 合成目标产物 2,3,4-Trifluorobromobenzene 主要起始原料 1,2,3-Trifluorobenzene
- (文献来源)合成步骤主要原料 1,2,3-Trifluorobenzene
2,3,4-三氟苯胺置于氢溴酸,Copper(I) Bromide,Sodium Nitrite体系中,化学反应生成2,3,4-三氟溴苯
参考文献:Novel 5-Amino-6-Methylquinolone Antibacterials: A New Class Of Non-6-Fluoroquinolones
标题:Novel 5-Amino-6-Methylquinolone Antibacterials: A New Class Of Non-6-Fluoroquinolones
摘要:A Novel 5-Amino-6-Methylquinoline Carboxylic Acid Was Synthesized From 2,3,4-Trifluoro Aniline In 12 Steps And Coupled With Various Types Of Amines To Furnish New Quinolone Antibacterial Agents. Depending On The Structure Of Amine,Some Of Quinolones Showed Comparable Activity To Ciprofloxacin Or Better Gram Positive Activity Than Ciprofloxacin,Demonstrating That The C6 Fluorine Atom Is Not A Necessary Requirement For Good Antibacterial Potency. (C) 1997 Elsevier Science Ltd.
Doi:10.1016/s0960-894X(97)00324-7
专利信息
专利号:US-2024101516-A1
优先权日:2021-01-20
标 题:Synthesis of polyfluorinated aryl and heteroaryl carboxamides
发明人:KADUSKAR RAHUL; BORATE KAILASKUMAR; ADHAV SUYOG; THIRUNAVUKKARASU SARAVANAN; SHINDE HARISH; GOETZ ROLAND
权利人:BASF SE
摘要:The presently claimed invention relates to a process for the preparation of mono-, di-, tri-, fluoro arylamide or hetroarylamide.
专利号:US-6870067-B2
优先权日:2002-10-08
标 题 :Process for the synthesis of trifluorophenylacetic acids
发明人:IKEMOTO NORIHIRO; DREHER SPENCER D
权利人:MERCK & CO INC
摘要:The present invention is concerned with a process for the preparation of trifluorophenylacetic acids using a Grignard reagent and an allylating agent, such as allyl bromide.
专利号:US-2021402380-A1
优先权日:2020-06-23
标 题 :Perovskites for photocatalytic organic synthesis
发明人:YAN YONG
权利人:SAN DIEGO STATE UNIV FOUNDATION
摘要:Nature is capable of storing solar energy in chemical bonds via photosynthesis through a series of C—C, C—O and C—N bond-forming reactions starting from CO 2 and light. Direct capture of solar energy for organic synthesis is a promising approach. Lead (Pb)-halide perovskite solar cells reach 24.2% power conversion efficiency, rendering perovskite a unique type material for solar energy capture. We show that photophysical properties of perovskites is useful in photoredox organic synthesis. Because the key aspects of these two applications are both relying on charge separation and transfer. Here we demonstrated that perovskites nanocrystals are exceptional candidates as photocatalysts for fundamental organic reactions, i.e. C—C, C—N and C—O bond-formations. Stability of CsPbBr 3 in organic solvents and ease-of-tuning their bandedges garner perovskite a wider scope of organic substrate activations.
专利号:WO-2023122754-A1
优先权日:2021-12-23
标 题 :Processes and intermediates for preparing gb13, gb22 and himgaline
发明人:LANDWEHR ELEANOR; SHENVI RYAN; BAKER MEGHAN; OGUMA TAKUYA
权利人:SCRIPPS RESEARCH INST
摘要:Provided herein are processes for the streamlined synthesis of Galbulimima alkaloids, such as himbadine, isolated from Galbulimima belgraveana and G. baccatta, trees endemic to the rainforests of Northern Australia and Papua New Guinea, as well as analogs thereof, such as GB13, GB16, GB22, and himgaline, and further including intermediates useful in the synthesis of these and related compounds.
专利号:US-8471057-B2
优先权日:2009-09-27
标 题:Sitagliptin intermediates, preparation methods and uses thereof
发明人:ZHU GUOLIANG; ZHANG JIAN; YANG LIJUN; YAO QINGDAN; YING JIE
权利人:ZHU GUOLIANG; ZHANG JIAN; YANG LIJUN; YAO QINGDAN; YING JIE; ZHEJIANG JIUZHOU PHARM CO LTD
摘要:The present invention relates to Sitagliptin intermediate and preparation method and use thereof. The method comprises reacting compound of formula (II) and trifluorobromobenzene with a Grignard reagent by a Grignard reaction to obtain a compound of formula (I). Compound of formula (I) is a new intermediate compound for the synthesis of Sitagliptin. Compound of formula (I) can be easily used for preparing another important intermediate compound of formula (V) for the synthesis of Sitagliptin. The structures of the compounds mentioned above are as the following:
专利号:KR-20230134489-A
优先权日:2021-01-20
标题:Synthesis of polyfluorinated aryl and heteroaryl carboxamides