CAS: 479-66-3; 3,7,8-Trihydroxy-3-Methyl-10-Oxo-1,3,4,10-Tetrahydropyrano[4,3-B]Chromene-9-Carboxylic Acid

该化合物是土壤,泥炭和其他有机物中由土质物质产生的自然产生的有机化合物,其特点是分子重量低,氧含量高,能够产生强大的发泡性,提高营养溶性与生物利用率;氟化酸有利于矿物和痕量元素跨细胞膜的运输,提高植物吸收率和代谢效率;其抗氧化特性通过促进微生物活动,有助于植物和土壤健康的压力抵抗;在农业应用中,氟化酸因其改善土壤结构,水保留和营养循环的能力而受到重视;其多变性延伸到园艺,水栽培和生物调节.

结构式图片

欧盟法规

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CAS号95730-73-7 1-(3,4-dimethox... | CAS号125288-40-6 1-[6'-benzyloxy...

合成工艺路线路线简述

    1-<6'-Benzyloxy-3',4'-Dimethoxy-2'-(Prop-1-Enyl)Phenyl>-4-(2-Methyl-1,3-Dioxolan-2-yl)Butane-1,3-Dione置于盐酸,Sodium Chlorite,Sodium Periodate,三氯化铝,二甲基硫,Oil Violet,硫酸,氨基磺酸,臭氧,溶剂黄146体系中,用 四氢呋喃,1,4-二氧六环,甲醇,乙醇,二氯甲烷,水,丙酮,甲苯 作为反应溶剂,化学反应 277.0H,反应生成 富里酸
    参考文献:含苯并吡喃酮杂环化合物的合成研究.第5部分.黄腐酸的全合成
    标题:含苯并吡喃酮杂环化合物的合成研究.第5部分.黄腐酸的全合成
    摘要:描述了黄腐酸(1A)的全合成.所述enedione(的区域选择性环化8F),所提出的生物遗传中间体(的等效图5A),用于citromycetin(2),得到吡喃酮(11A),这导致了富里酸(1A通过涉及脱苄基化,选择性臭氧化的路径),和保湿.
    DOI:10.1039/p19870000389

    海关参考信息

    专利信息


    专利号:US-2023119068-A1
    优先权日:2020-02-13
    标题:Methods for rapid synthesis of pyranoanthocyanins
    发明人:ZHU XIAOYI; STRAATHOF NICOLE; MIYAGUSUKU-CRUZADO GONZALO; GIUSTI M MONICA; CANO ISRAEL GARCIA; JIMENEZ-FLORES RAFAEL
    权利人:OHIO STATE INNOVATION FOUNDATION
    摘要:The present disclosure provides methods for the rapid synthesis of pyranoanthocyanins.

    专利号:US-4592814-A
    优先权日:1983-05-23
    标题:Electrochemical synthesis of humic acid and other partially oxidized carbonaceous materials
    发明人:VAUGHAN RONALD J; BY BANK OF AMERICA NT SA ADMIN
    权利人:CHEVRON RES
    摘要:A continuous cyclic electrolytic/carbon oxidation process wherein ferrous ion is oxidized at the anode and hydrogen is generated at the cathode of an electrolytic cell. The ferric ions produced at the anode are thereafter reduced to ferrous ions by contact with a solid carbonaceous material and the ferrous ions recycled for electrochemical reoxidation. The process produces partially oxidized organic products from the combustion process in high yield.

    专利号:WO-2024259491-A1
    优先权日:2023-06-23
    标 题:New synthesis method
    发明人:FORD DANIEL; POZNAKS VIKTORS; FOTINS JURIS; ÄŒERÅ…AKS DMITRIJS
    权利人:THE HEART RES INSTITUTE LTD
    摘要:The present disclosure generally relates to a process for the synthesis of AZD6482. In particular, the present disclosure also relates to a process for the synthesis of enantiomerically pure AZD6482. The present disclosure also relates to a process for the synthesis of enantiomerically pure intermediates. The present disclosure also relates to compounds prepared by the processes and the use of such compounds to prepare compositions and to treat disorders.

    专利号:US-2025197439-A1
    优先权日:2022-03-18
    标 题:Decarboxylative acetoxylation using mn(ii) or mn(iii) reagent for synthesis of 4'-acetoxy-nucleoside and use thereof for synthesis of corresponding 4'-(dimethoxyphosphoryl)methoxy-nucleotide
    发明人:VAGLE KURT EDRIC; BHADURI SAYANTAN; YANG GUOHAN
    权利人:DICERNA PHARMACEUTICALS INC
    摘要:The present invention relates to the preparation of nucleic acids, nucleosides, nucleotides, and analogues thereof useful as potent and stable RNA interference agents. The present invention provides improved yields and avoids the use of lead tetraacetate for decarboxylative acetylation which decreases the overall cost of production by removing the need for lead remediation and offers a significant reduction in the environmental costs in production.

    专利号:US-12275733-B2
    优先权日:2016-11-07
    标 题:Substituted pyrido[3,4-b]indoles for the treatment of cartilage disorders
    发明人:GRETZKE DIRK; RITZELER OLAF; HEINELT UWE; WEHNER VOLKMAR; SCHMIDT FRIEDEMANN
    权利人:SANOFI SA
    摘要:The present invention relates to 8-aryl-substituted and 8-heteroaryl-substituted 9H-pyrido[3,4-b]indoles of the formula (I), in which A, E, G, R1 to R6 and R10 are as defined in the claims, which stimulate chondrogenesis and cartilage matrix synthesis and can be used in the treatment of cartilage disorders and conditions in which a regeneration of damaged cartilage is desired, for example joint diseases such as osteoarthritis. The invention furthermore relates to processes for the synthesis of the compounds of the formula (I), their use as pharmaceuticals, and pharmaceutical compositions comprising them.

    专利号:WO-2025088147-A1
    优先权日:2023-10-27
    标题 :Theranostic psma-targeting ligands for the diagnosis and treatment of psma-expressing cancers and their solid phase synthesis
    发明人:Schäfer Martin; BAUDER-WUEST ULRIKE; ROSCHER MAREIKE; REMDE YVONNE; BENEÅ OVÃ?-SCHÄFER MARTINA; BARINKA CYRIL; KUTILOVÃ? ZSÓFIA; MOTLOVÃ? LUCIA
    权利人:DEUTSCHES KREBSFORSCHUNGSZENTRUM STIFTUNG DES OEFFENTLICHEN RECHTS
    摘要:The present invention generally relates to the field of radiopharmaceuticals and their use in nuclear medicine as tracers, imaging agents and radiopharmaceuticals for the treatment of various disease states of PSMA-expressing cancers, especially prostate cancer, and metastases thereof. Further the present invention provides synthetic procedures for the synthesis of such PSMA-targeting ligands.
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    主要参考文献

    参考标题:Total Synthesis Of Fulvic Acid
    作者:Masashige Yamauchi,Sadamu Katayama,Toshiharu Todoroki,Toshio Watanable
    摘要:Synthesis Of Fulvic Acid (1A) Was Accomplished By A Route Involving Selective Ozonization Of 9-Propenylpyranobenzopyran (1C), Obtained By A Regioselective Cyclization Of The 2-Methylsulphinylmethyl 1,3-Dione(3C).

    合成参考文献


    参考文献:10.1007/s004410051341
    摘要:Ioannidis N, Kurz B, Hansen U, Schünke M. Influence of fulvic acid on the collagen secretion of bovine chondrocytes in vitro. Cell Tissue Res. 1999 Jul;297(1):141–7. doi: 10.1007/s004410051341.
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