CAS: 675-14-9; 2,4,6-Trifluoro-1,3,5-Triazine

相似化合物

7709-13-9 933-20-0 30894-74-7

上下游产品

CAS号108-77-0 氰尿酰氯 | CAS号7783-56-4 三氟化锑 | CAS号7783-60-0 四氟化硫 | CAS号1495-50-7 cyanogen fluoride | CAS号696-85-5 2-chloro-4,6-di... | CAS号696-84-4 2,4-dichloro-6-... | CAS号506-78-5 碘化氰 | CAS号7276-63-3 bis{bis(trifluo... | CAS号506-77-4 氯化氰 | CAS号102-54-5 二茂铁 | CAS号1973-05-3 N2,N4,N6-三苯基-1,... | CAS号7783-54-2 三氟化氮 | CAS号75-73-0 四氟化碳 | CAS号666-95-5 Perfluor-(1,4-d... | CAS号1495-50-7 cyanogen fluoride | CAS号353-85-5 三氟乙腈 | CAS号371-71-1 1,1-difluoro-N-... | CAS号877-89-4 三聚氰酸三甲酯

碘化氰置于mercury(II) Fluoride体系中,用 Neat (No Solvent) 作为反应溶剂,化学反应生成 三聚氟氰
参考文献:Hueckel,W.,1946,P. 36-37
标题:Hueckel,W.,1946,P. 36-37

专利信息

专利号:US-2021053913-A1
优先权日:2019-08-22
标题 :Process for the Synthesis of Fluorinated Conductive Salts for Lithium Ion Batteries
发明人：ZHOU CHANGYUE; DU HONGJUN; WU WENTING
权利人:FUJIAN YONGJING TECH CO LTD
摘要:The invention relates to a new process for the synthesis of fluorinated conductive salts for lithium ion batteries (Li-ion batteries). The said fluorinated conductive lithium ion (Li-ion) battery salts of interest in the framework of the present inventions synthesis process, for example, are Li-ion salts such as LiFSI (lithium bis-(fluoromethanesulfonlyl) imide), LiTFSI (lithium bis-(trifluormethanesulfonlyl) imide), and LiTFSFI (lithium trifluoromethanesulfonylfluorosulfonyl imide), with the formulas as displayed in the Table I herein below. LiFSI, LiTFSI and LiFSTFSI are the most promising conducting salts for Lithium ion batteries and essential for future electromobility.

专利号:US-2023286918-A1
优先权日:2020-07-02
标 题:Manufacturing process for 3,5-dichloropicolinonitrile for synthesis of vadadustat
发明人：JURKAUSKAS VALDAS; JUNG YOUNG CHUN; KWON TAESOO; KANNAN ARUNACHALAM; GONDI VIJAYA BHASKER
权利人:AKEBIA THERAPEUTICS INC
摘要:Disclosed herein are methods and processes of preparing vadadustat or a pharmaceutically acceptable salts thereof, and intermediates (e.g., a compound of Formula (I), (I-F), (II), or (IV), or a pharmaceutically acceptable salts thereof) useful for the synthesis of vadadustat.

专利号:US-3641020-A
优先权日:1969-01-23
标 题 :Synthesis of cyanuric fluoride
发明人：ANDERSON RICHARD W; FRICK HUGHIE R
权利人:DOW CHEMICAL CO
摘要:A PROCESS FOR THE EFFICIENT SYNTHESIS OF CYANURIC FLUORIDE IS PROVIDED. THE PROCESS COMPRISES CONTACTING CERTAIN CYANURIC HALIDES WITH SELECTED ALKALI METAL FLUORIDES IN THE PRESENCE OF A PERHALOCARBONYL COMPOUND. THE PROCESS OF THE PRESENT INVENTION PROVIDES FOR THE PRODUCTION OF CYANURIC FLUORIDE AT CONSIDERABLY REDUCED TEMPERATURES, THAN THOSE USED IN KNOWN PROCESSES.

专利号:US-2008221303-A1
优先权日:2004-02-18
标 题:Method for the Preparation of Peptide-Oligonucleotide Conjugates
发明人：KATZHENDLER JEHOSHUA; KLAUZNER YAKIR; BEYLIS IRENA; MIZHIRITSKII MICHAEL; SHPERNAT YAACOV; ASHKENAZI BORIS; FRIDLAND DMITRI
权利人:KATZHENDLER JEHOSHUA; KLAUZNER YAKIR; BEYLIS IRENA; MIZHIRITSKII MICHAEL; SHPERNAT YAACOV; ASHKENAZI BORIS; FRIDLAND DMITRI
摘要:The present invention relates to the synthesis of peptide-oligonucleotide conjugates (POC). More specifically, the invention relates to a novel method for the preparation of peptide-oligonucleotide conjugates, which can be conducted under mild conditions on solid support, can be performed manually or by a synthesizer, can be used to synthesize alternating sequences of peptides and oligonucleotides, and is applicable to the synthesis of a wide variety of peptide-oligonucleotide conjugates constructed from alternate peptide and oligonucleotide blocks.

专利号:US-2025188022-A1
优先权日:2022-02-07
标 题 :Process for the preparation of nafamostat, camostat and their derivatives
发明人：AHMED RIYAZ; KUMAR GULSHAN; MAHAJAN SHEENA; Verma Praveen Kumar; CHAM PANKAJ SINGH; KUMAR AMIT; AHMED QAZI NAVEED; REDDY DUMBALA SRINIVASA; SHANKAR RAVI; SINGH PARVINDER PAL
权利人:COUNCIL SCIENT IND RES
摘要:The invention provides a novel, economical and practical route for the synthesis of an ester from acid and alcoholic functionalities using Trihalotriazine as coupling agent. Specifically, the invention provides a novel, economical and practical route for the preparation of Nafamostat and Camostat. Synthesis of p-guanidinobenzoic acid (Al) was also achieved from thiourea and p-aminobenzoic acid by using trihalotriazine as coupling reagent.

专利号:US-2022233673-A1
优先权日:2019-06-04
标 题:METHODS OF PRODUCING SHIGA TOXIN B-SUBUNIT (STxB) MONOMERS AND OLIGOMERS, AND USES THEREOF
发明人：BILLET ANNE; SCHMIDT FRÉDÉRIC; JOHANNES LUDGER; SERVENT DENIS; MOURIER GILLES; TARTOUR ÉRIC; KAY MICHAEL; FULCHER JAMES M
权利人:INST CURIE; CENTRE NAT RECH SCIENT; INST NAT SANTE RECH MED; COMMISSARIAT A LENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES CEA; APHP ASSIST PUBLIQUE HOPITAUX DE PARIS; UNIV PARIS; UNIV OF UTAH RESEARCH FOUDATION; UNIV UTAH RES FOUND
摘要:A method of producing a monomer of a Shiga toxin B-subunit (STxB) protein or of a variant thereof by peptide chemical synthesis, as well as to a method of producing a pentamer of the STxB protein or of the variant thereof. The methods are particularly advantageous as they overcome major issues typically observed in peptide chemical synthesis, including solubility and purity issues.