CAS: 37617-03-1; Undec-2-En-1-Ol

该化合物是被归类为不饱和酒精的有机化合物,其特点是存在双重结合和羟基(-OH)组,其特点是由11个碳原子组成的线性碳链,其二至三碳原子之间在链端的二至三碳原子之间有双重结合.这一结构具有特定的物理特性,例如,与类似分子重量的饱和酒精相比,沸点相对较低,而且通常在室温下,黄色液体不色,不色. 2-Undecen-1-ol在有机溶剂中溶解,并由于氢氧基组的盐分性质,在水中表现出中等溶解性.它被用于各种用途,包括作为红味,表面活性剂和其他有机化合物合成的化学中间体.此外,其不饱和度允许进一步的化学再活性,使其在有机合成中成为多种化合物.在处理时,应参考安全数据,因为如果浸入或吸入,可能会对健康造成危害.

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°Ctylmagnesium bromide acrolein 1-bromo-2-undecene methyl undec-2-enoate2-undecenal 3,5-dinitro-benzoic acid undec-2-enyl ester 1-bromo-2-undecene 2-(10-methoxycarbonyldecyl)-1,3-dioxolane

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    专利信息


    专利号:US-8865624-B2
    优先权日:2010-09-01
    标题 :Inhibitor for tobacco axillary bud growth and method for inhibiting tobacco axillary bud growth
    发明人:TANAKA MOTOKI; TANAKA KEIJITSU; SHIBUYA TAKESHI; IKUTA EIJI; YOSHINAGA KOTARO; YAMAGUCHI YUKI
    权利人:TANAKA MOTOKI; TANAKA KEIJITSU; SHIBUYA TAKESHI; IKUTA EIJI; YOSHINAGA KOTARO; YAMAGUCHI YUKI; SDS BIOTECH CORP
    摘要:The present invention relates to an inhibitor for tobacco axillary bud growth, the inhibitor comprising, as an active ingredient, one or more kinds of very-long chain fatty acid synthesis inhibitors such as a chloroacetamide-based herbicide, fentrazamide, cafenstrole or indanofan; an inhibitor for tobacco axillary bud growth, the inhibitor comprising the aforesaid very-long chain fatty acid synthesis inhibitor together with clorthal-dimethyl or an aliphatic alcohol having 6 to 20 carbon atoms; and a method for inhibiting tobacco axillary bud growth which comprises applying the inhibitor for tobacco axillary bud growth. The inhibitor for tobacco axillary bud growth of the present invention shows sustained drug efficacy at a low concentration, induces neither chemical injury nor disease, and can contribute to the improvement in labor productivity.

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    合成参考文献


    摘要:The Good Scents Company Information System
    摘要:Milata, V.; Rádl, S.; Voltrová, S., Science of Synthesis, (2008) 32, 598.
    摘要:Braun, M., Science of Synthesis, (2007) 35, 435.
    摘要:Eames, J., Science of Synthesis, (2008) 36, 440.
    摘要:Hodgson, D. M.; Humphreys, P. G., Science of Synthesis, (2008) 36, 611.
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