CAS: 14970-87-7; 3,6-Dioxa-1,8-Octanedithiol

相似化合物

2781-02-4 56282-36-1 194425-46-2

上下游产品

1,2-bis(2-chloroethoxy)ethane 2,2'-[1,2-ethanediylbis(oxy)]bisethanol 1,2-bis-(2-bromo-ethoxy)-ethane triethylene glycol di-(p-toluenesulfonate) 3-Phenyl-1,7-dithia-15-crown-5 4-(1,4-dioxa-7,13-dithia-10-azacyclopentadecan-10-yl) benzaldehyde 1,8-bis(o-hydroxyphenylthio)-3,6-dioxa°Ctane

三乙二醇置于盐酸,Sodium Iodide,Potassium Hydroxide体系中,用 甲醇,二氯甲烷,水,丙酮 用作溶剂,化学反应 24.0H,反应生成2,2'-(1,2-乙二基双氧代)双乙硫醇
参考文献:制备6(i)-(ω-亚硫烷基-亚烷基-亚硫烷基)-β-环糊精衍生物的优化方法.
标题:制备6(i)-(ω-亚硫烷基-亚烷基-亚硫烷基)-β-环糊精衍生物的优化方法.
摘要:描述了制备在6位上连接有巯基的单取代β-环糊精衍生物的通用高产率方法.巯基通过不同长度和重复单元(乙二醇或亚甲基)的连接基连接.通过ir,Ms和NMR光谱表征目标化合物.提出了将其完全转化为相应的二硫化物的简单方法,以及将二硫化物还原成硫醇的方法.硫醇和二硫化物都是可用于环糊精与金或聚多巴胺涂覆的固体表面的明确共价连接的衍生物.
Doi:10.3762/bjoc.12.38

专利信息

专利号:US-2024309024-A1
优先权日:2023-03-14
标题 :Direct synthesis of alkenylhalosilanes
发明人：LEWIS KENRICK MARTIN; ZHU YANJUN; BYRNE CHRISTOPHER M
权利人:MOMENTIVE PERFORMANCE MAT INC
摘要:A process for the direct synthesis of alkenylhalosilane monomers. Forming a slurry of liquid and copper-activated silicon from fresh silicon, cyclone fines and/or fine dust from silicon grinding, ultrafines and/or spent contact mass from the Direct Synthesis of alkylhalosilanes and arylhalosilanes, in a thermally stable solvent. Reacting the silanes by agitating the slurry with at least one unsaturated aliphatic or cycloaliphatic organohalide of the formula R1X, and optionally an organohalosilane and/or hydrogen halide, in the presence of a polymerization inhibiting Lewis base additive, at a reaction time, temperature and pressure effective to produce alkenylhalosilanes having the formulae, R1SiHX2, R12SiHX, R13SiX, R1SiX3, and R12SiX2 or mixtures thereof.

专利号:WO-2025188688-A8
优先权日:2024-03-04
标题 :Rapid synthesis of degradable polyols based on esters and thioethers for use in polyurethanes
发明人：Monroe Mary Beth; PETRYK NATALIE M
权利人:Monroe Mary Beth; PETRYK NATALIE M
摘要:A degradable polyurethane (PUr) having degradation rates useful for hemostatic dressings for controlling bleeding in traumatic wounds. Degradable PUrs may be synthesized from degradable monomers based on hydrolytically labile esters and oxidatively labile thioethers using rapid click-chemistry reactions. Monomers may include trimethylolpropane tris(3-mercaptopropionate) (TMPMP), dipentaerythritol hexakis(3-mercaptopropionate) (DPEHMP), dipentaerythritol hexakis(3-mercaptopropionate) (DPEHMP) or 2,2'-(ethylenedioxy) diethanethiol reacted with hydroxyethyl acrylate, 3-buten-1-ol, 3-methyl-3-buten-1-ol, or 3-buten-2-ol. Synthesis of these monomers is rapid and has no byproducts or toxic catalysts that require removal, enabling polyol synthesis and immediate use in further polymerization

专利号:US-2023331778-A1
优先权日:2020-08-31
标 题 :An improved process for fmoc synthesis of etelcalcetide
发明人：LOBO LESTER JOHN; CHANDRAKESAN MURALIDHARAN; DOSHI CHETAN; CHANADAK SHAILESH LALCHAND; YADAV NANDLAL GOPAL; MOHE NIKHIL UMESH; VISHWANATHAN KODANDARAMAN; CHAVRE PRAFUL SHAMRAO
权利人:USV PRIVATE LTD
摘要:The present invention relates to an improved process for the synthesis of Etelcalcetide and its analogs by solid phase synthesis of Fmoc protected amino acids in a sequential manner, followed by acetylation of terminal D-cys and cleavage of peptide from solid support. The crude heptapeptide thus obtained is reduced using Tris(2-carboxyethyl) phosphine hydrochloride, purified and oxidized with L-cysteine. The oxidized Etelcalcetide is purified and salt exchanged using a one-step reverse phase chromatography process. The purified Etelcalcetide hydrochloride is then precipitated using organic solvents, concentrated and lyophilized to purity of greater than 99.0%.

专利号:US-9920160-B2
优先权日:2014-09-03
标题 :Method for synthesis of polymer containing multiple epoxy groups
发明人：GAO CHAO; ZHENG YAOCHEN; PENG LI; CAI SHENGYING; WENG ZHULIN
权利人:UNIV ZHEJIANG
摘要:A method for a synthesis of a polymer containing multiple epoxy groups includes steps of: under protection of nitrogen or argon, with a photosensitive free radical initiator under an ultraviolet light irradiation, initiating a mixture of a dithiol compound and alkynyl glycidyl ether or other alkynyl-containing compounds to proceed a thiol-yne polymerization, so as to obtain the polymer. The number of the epoxy groups is able to be adjusted through changing a type of a dithiol monomer, a mixing ratio of the dithiol monomer, and a mixing ratio between the alkynyl glycidyl ether and other alkynyl compounds. The present invention has advantages of: fast reaction, convenient process, easy post-processing, a large number of the epoxy groups, and adjustable and controllable content. The obtained polymer has a wide potential application in fields of coating, adhesive, ink, encapsulating material, resin for composite material, additive, high performance material, function material, and so on.

专利号:US-2021130409-A1
优先权日:2017-09-01
标 题 :Method for the Solid-Phase Synthesis of Cyclic Pentapeptides
发明人：ZHENGGUO JIANG; LUCIANO FORNI; ROBERTSON ALAN
权利人:Alsonex Pty Ltd
摘要:A method for the synthesis of a cyclic ornithine-proline-D-cyclohexylalanine-tryptophan-arginine pentapeptide of Formula A; n n n n n n n n n n n n wherein R 1 and R 2 are, independently, —H, or —C(O)R 3 where R 3 is —CH 2 Ph, —CH 2 CH 2 Ph, —CHâ•?CHPh, —C(NHAC)CH 2 Ph;n nthe method comprising the steps of;n nforming a linear proline-D-cyclohexylalanine-tryptophan-arginine-ornithine pentapeptide of Formula B, attached to a polymeric resin;n n n n n n n n n n n n n n n n n wherein R 1 is as for Formula A, RES indicates the polymeric resin, and P 1 and P 2 are protecting groups;n ncyclising the linear pentapeptide of Formula B to form a cyclic pentapeptide of Formula C, attached to the polymeric resin;n n n n n n n n n n n n n n n cleaving the cyclic peptide of Formula C from the resin providing a cleaved cyclic pentapeptide having a free amine group of an ornithine residue;n noptionally substituting the free amine group of the ornithine residue of the cleaved cyclic peptide;n nremoving the protecting groups P 1 and P 2 , to providethe cyclic peptide of Formula A.

专利号:US-2025282813-A1
优先权日:2021-04-09
标 题 :Pseudo solid phase protecting group and methods for the synthesis of oligonucleotides and oligonucleotide conjugates
发明人：OKADA YOHEI; SUZUKI HIDEAKI; LUTHER ANATOL
权利人:BACHEM HOLDING AG
摘要:A novel pseudo solid phase protecting group and methods for the synthesis of oligonucleotides and oligonucleotide conjugates are provided. The pseudo solid phase protecting group is represented by formula II wherein: * indicates the point of attachment to an oxygen atom of a hydroxyl moiety of the nucleoside, the nucleotide, the oligonucleotide, or of the conjugate of a nucleoside, a nucleotide or an oligonucleotide to be protected; c is 0 or 1; a is an integer of 1 to 12; R3 is H; R5 is O—R6 or H, where R6 is a C8-C40 aliphatic hydrocarbon group; each of R4 is independently O—R6, where R6 is at each occurrence independently a C8-C40 aliphatic hydrocarbon group; b is 1 to 3; with the proviso that if b is 1, at least one of R3 and R5 is not H; and with the further proviso that the sum of all carbon atoms contained in the R3, R4, and R5 moieties present is larger than 23 and smaller than 200.