CAS: 532-34-3; Butopyronoxyl

该化合物是一种合成有机化合物,通常用作昆虫驱虫剂,对蚊虫和其他飞虫特别有效,其化学结构以丁基和高温类为主,有助于其挥发性和驱虫性.该化合物往往被纳入个人防护产品的配方,如乳液和喷雾,因为它能够震慑昆虫,而不会对人类或环境造成重大伤害.Butoyronoxyl 因其稳定性和相对较低的毒性而备受重视,因此适合在各种气候和条件下使用.其功效和安全性简介将它确定为可靠的昆虫控制应用选择.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

di-n-butyl oxalateH-pyran-2-carboxylic acid butyl ester6,6-dimethyl-4-phenylhydrazono-5,6-dihydro-4H-pyran-2-carboxylic acid butyl ester pyran4,4-Dimethyl-2,6-dioxo-4,5-dihydrofuro3,4-bpyran

合成工艺路线路线简述

    📜草酸二丁酯,Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于sodium Butanolate体系中,化学反应生成 避虫酮
    参考文献:Butyl Esters Of Alpha,Alpha-Dimethyl-Alpha-Carboxydihydro-Gammapyrone And To Process For Making The Same
    标题:Butyl Esters Of Alpha,Alpha-Dimethyl-Alpha-Carboxydihydro-Gammapyrone And To Process For Making The Same

    海关参考信息

    专利信息


    专利号:WO-2017077549-A1
    优先权日:2015-11-02
    标题 :Analogues of angiopterlactone b and a process for the synthesis thereof
    发明人:BHATTACHARYA ASISH KUMAR; KOTAMMAGARI THARUN KUMAR
    权利人:COUNCIL SCIENT IND RES
    摘要:The invention discloses a novel analogues of Angiopterlactone B of formula (I) and process for the synthesis thereof. Further the present invention discloses a total synthetic one pot process for the synthesis of Angiopterlactone B and its analogues comprises the reaction of the dihydro pyronones with Tetra-n-butylammonium fluoride (TBAF) in dry solvent for the time period ranging from 1-2 hours at the temperature ranging from 20-30°C, working up and subjecting the residue to column chromatography to obtain the product.

    专利号:WO-2025056767-A1
    优先权日:2023-09-15
    标题 :Process for the preparation of enantiomerically enriched aliphatic amines
    发明人:BOU HAMDAN FARHAN; GODINEAU EDOUARD; SMEJKAL TOMAS; DUMEUNIER RAPHAEL; BOUSSEMGHOUNE MOHAMED ABDELOUAHAB; BLUM MATHIAS
    权利人:SYNGENTA CROP PROTECTION AG
    摘要:The present invention relates to a process for the preparation of enantiomerically enriched cyclobutylamines of formula (I) from α-tertiary cyclobutanones and reacting said enantiomerically enriched cyclobutylamines to enantiomerically enriched cyclobutylamides. Such compounds are useful intermediates in the synthesis of microbiocidal thiazole compounds.

    专利号:WO-9848791-A1
    优先权日:1997-04-30
    标 题:Synthesis of discodermolide and analogs
    发明人:MYLES DAVID C; HARRIED SCOTT S; YANG GE
    权利人:UNIV CALIFORNIA; MYLES DAVID C; HARRIED SCOTT S; YANG GE
    摘要:A method for making discodermolide and analogs thereof. The method utilizes three precursors which correspond to three subparts of discodermolide which are formed by disconnecting the discodermolide carbon backbone at positions C-7 to C-8 and C-15 to C-16. Coupling of the precursors is accomplished using chelation-controlled alkylation.

    专利号:US-2005043376-A1
    优先权日:1996-12-03
    标题:Synthesis of epothilones, intermediates thereto, analogues and uses thereof
    发明人:DANISHEFSKY SAMUEL J; BERTINATO PETER; SU DAI-SHI; MENG DONGFANG; CHOU TING-CHAO; KAMENECKA TED; SORENSEN ERIK J; BALOG AARON; SAVIN KENNETH A
    摘要:The present invention provides convergent processes for preparing epothilone A and B, desoxyepothilones A and B, and analogues thereof. Also provided are analogues related to epothilone A and B and intermediates useful for preparing same. The present invention further provides novel compositions based on analogues of the epothilones and methods for the treatment of cancer and cancer which has developed a multidrug-resistant phenotype.

    专利号:US-RE41990-E
    优先权日:1996-12-03
    标 题 :Synthesis of epothilones, intermediates thereto, analogues and uses thereof
    发明人:DANISHEFSKY SAMUEL J; BERTINATO PETER; SU DAI-SHI; MENG DONGFANG; CHOU TING-CHAO; KAMENECKA TED; SORENSEN ERIK J; BALOG AARON; SAVIN KENNETH A
    权利人:SLOAN KETTERING INST CANCER
    摘要:The present invention provides convergent processes for preparing epothilone A and B, desoxyepothilones A and B, and analogues thereof. Also provided are analogues related to epothilone A and B and intermediates useful for preparing same. The present invention further provides novel compositions based on analogues of the epothilones and methods for the treatment of cancer and cancer which has developed a multidrug-resistant phenotype.

    专利号:EP-1058679-B1
    优先权日:1998-02-25
    标 题 :Synthesis of epothilones, intermediates thereto and analogues therof
    发明人:DANISHEFSKY SAMUEL J; BALOG AARON; BERTINATO PETER; SU DAI-SHI; CHOU TING-CHAU; MENG DONGFANG; KAMENECKA TED; SORENSEN ERIK J; KUDUK SCOTT; HARRIS CHRISTINA; ZHANG XIU-GUO; BERTINO JOSEPH R
    权利人:SLOAN KETTERING INST CANCER
    摘要:The present invention provides convergent processes for preparing epothilone A and B, desoxyepothilones A and B, and analogues thereof, useful in the treatment of cancer and cancer which has developed a multidrug-resistant phenotype. Also provided are intermediates useful for preparing said epothilones.

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 9th ed. Volumes 1-3. New York, NY: Van Nostrand Reinhold, 1996., p. 586
    摘要:Gosselin, R.E., R.P. Smith, H.C. Hodge. Clinical Toxicology of Commercial Products. 5th ed. Baltimore: Williams and Wilkins, 1984., p. II-345
    摘要:Franke C et al; Chemosphere 29: 1501-14 (1994)
    摘要:Worthing, C. R. (ed.). Pesticide Manual. 6th ed. Worcestershire, England: British Crop Protection Council, l979., p. 66
    摘要:Mill T et al; Environmental Fate and Exposure Studies Development of a PC-SAR for Hydrolysis: Esters, Alkyl Halides and Epoxides. EPA Contract No. 68-02-4254. Menlo Park, CA: SRI International (1987)
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