CAS: 1330-85-4; (Dodecylbenzyl)Trimethylammonium Chloride

该化合物是一种作为表面活性剂和相向转移催化剂常用的四铵化合物,其特点是附于一个苯基组的长的疏水多丁基链,加上氮原子上的三个甲基组,从而助长了其非物理性质.这一结构使得它能够有效地减少表面紧张,提高各种溶剂的溶解性.该化合物一般是白色的,对非白色的固体或粘粘液,视温度而定.在水和有机溶剂中可以溶解,能够适用于清洁剂,乳化剂和分异剂.此外,它显示出抗微生物特性,可以对各种工业和家庭清洁产品有益.然而,与许多四氟化铵化合物一样,它可能会对水生生物造成环境关切和潜在毒性,需要谨慎处理和处置.

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    专利信息


    专利号:US-7935704-B2
    优先权日:2003-08-01
    标 题 :Dehydrophenylahistins and analogs thereof and the synthesis of dehydrophenylahistins and analogs thereof
    发明人:PALLADINO MICHAEL A; LLOYD GEORGE KENNETH; HAYASHI YOSHIO; NICHOLSON BENJAMIN
    权利人:NEREUS PHARMACEUTICALS INC
    摘要:Compounds represented by the following structure (I) are disclosed: n nas are methods for making such compounds, wherein said methods comprise reacting a diacyldiketopiperazine with a first aldehyde to produce an intermediate compound; and reacting the intermediate compound with a second aldehyde to produce the class of compounds with the generic structure, where the first aldehyde and the second aldehydes are selected from the group consisting of an oxazolecarboxaldeyhyde, imidazolecarboxaldehyde, a benzaldehyde, imidazolecarboxaldehyde derivatives, and benzaldehyde derivatives, thereby forming the above compound wherein R 1 , R 1 ′, R 1 ″, R 2 , R 3 , R 4 , R 5 , and R 6 , X 1 and X 2 , Y, Z, Z 1 , Z 2 , Z 3 , and Z 4 may each be separately defined in a manner consistent with the accompanying description. Compositions and methods for treating vascular proliferation are also disclosed.

    专利号:US-7956058-B2
    优先权日:2002-08-02
    标 题:Dehydrophenylahistins and analogs thereof and the synthesis of dehydrophenylahistins and analogs thereof
    发明人:HAYASHI YOSHIO; PALLADINO JR MICHAEL A; GRODBERG JENNIFER
    权利人:NEREUS PHARMACEUTICALS INC
    摘要:Compounds represented by the following structure (I) are disclosed: n nas are methods for making such compounds, wherein said methods comprise reacting a diacyldiketopiperazine with a first aldehyde to produce an intermediate compound; and reacting the intermediate compound with a second aldehyde to produce the class of compounds with the generic structure, where the first aldehyde and the second aldehydes are selected from the group consisting of an oxazolecarboxaldeyhyde, imidazolecarboxaldehyde, a benzaldehyde, imidazolecarboxaldehyde derivatives, and benzaldehyde derivatives, thereby forming the above compound wherein R 1 , R 1 ′, R 1 ′, R 2 , R 3 , R 4 , R 5 , and R 6 , X 1 and X 2 , Y, Z, Z 1 , Z 2 , Z 3 , and Z 4 may each be separately defined in a manner consistent with the accompanying description. Compositions and methods for treating cancer and fungal infection are also disclosed.

    专利号:US-10434098-B2
    优先权日:2015-06-02
    标 题 :Deuterated dehydrophenylahistin compounds and preparation method thereof and use thereof in preparation of anti-tumor drugs
    发明人:LI WENBAO; SUN TIANWEN; WANG SHIXIAO; ZHAO JIANCHUN; CAI BING; GUAN HUASHI
    权利人:MARINE BIOMEDICAL RES INST QINGDAO CO LTD
    摘要:Provided are a deuterium-substituted dehydrophenylahistin-like compound, preparation method thereof and use in a preparation of antitumor drugs. The deuterium-substituted dehydrophenylahistin-like compound has a structure of general formula (I), and a synthesis method thereof comprises: firstly conducting a condensation reaction of diacetyldiketopiperazine and an aldehyde intermediate a or a deuterated aldehyde compound b to form a heterocyclic compound c or a deuterium-containing heterocyclic compound d, which is then subjected to a condensation reaction with benzaldehyde and a deuterium-substituted benzaldehyde-like compound to form the deuterium-substituted dehydrophenylahistin-like compound. Also provided are a highly effective deuterated aldehyde intermediate with a high deuterium substitution rate and a deuterium-containing heterocycle intermediate, and a synthesis method thereof. An experiment shows that the deuterium-substituted dehydrophenylahistin-like compound provided by the present invention has an effect on tubulin depolymerization and can treat a refractory solid tumor or lymphoma. The present invention provides a method for researching and developing antitumor drugs of the related compound.

    专利号:US-2005197344-A1
    优先权日:2003-08-01
    标题 :Dehydrophenylahistins and analogs thereof and the synthesis of dehydrophenylahistins and analogs thereof

    专利号:US-2006223823-A1
    优先权日:2002-08-02
    标 题 :Dehydrophenylahistins and analogs thereof and the synthesis of dehydrophenylahistins and analogs thereof

    专利号:US-2006217553-A1
    优先权日:2002-08-02
    标 题 :Dehydrophenylahistins and analogs thereof and the synthesis of dehydrophenylahistins and analogs thereof

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    合成参考文献


    参考文献:10.1007/978-981-16-3307-2_18
    摘要:Devi P, Thakur N. Bioprospecting of Marine Fungi. 2021. In: Progress in Mycology.
    参考文献:10.1007/978-3-030-54027-2_17
    摘要:Pal D, Raj K. Biological Activities of Marine Products and Nutritional Importance. 2020 Dec 15. In: Advanced Structured Materials.
    参考文献:10.1007/978-3-030-19030-9_18
    摘要:Giddings L, Newman DJ. Bioactive Compounds from Extremophilic Marine Fungi. 2019. In: Fungi in Extreme Environments: Ecological Role and Biotechnological Significance.
    参考文献:10.1007/978-3-030-90383-1_17
    摘要:Thissera B, Sayed AM, Hassan HM, Abdelmohsen UR, Ebel R, Jaspars M, Rateb ME. The Hidden Treasure: Marine Microbiome as Repository of Bioactive Compounds. 2022. In: The Microbiomes of Humans, Animals, Plants, and the Environment.
    参考文献:10.1007/s11696-023-02742-2
    摘要:Chen H, Liu Y, Jiang R, Yu X, Qin M, Gong P. Improved protocol for synthesizing (3Z,6Z)-3-benzylidene-6-[(5-tert-butyl-1H-imidazol-4-yl)methylidene]piperazine-2,5-dione (plinabulin). Chem. Pap. 2023 Apr 08;77(7):3803–10. doi: 10.1007/s11696-023-02742-2.
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