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1,1-Difluorododecane | 62127-45-1

中文名称
——
中文别名
——
英文名称
1,1-Difluorododecane
英文别名
——
1,1-Difluorododecane化学式
CAS
62127-45-1
化学式
C12H24F2
mdl
——
分子量
206.319
InChiKey
JTKAJWQYBOFEEW-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    261.3°C (rough estimate)
  • 密度:
    0.8923 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    6.7
  • 重原子数:
    14
  • 可旋转键数:
    10
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    十二醛二乙胺基三氟化硫 作用下, 以 二氯甲烷 为溶剂, 生成 1,1-Difluorododecane
    参考文献:
    名称:
    烷基 CF 基团的三硫脱氟
    摘要:
    报道了一种用氚/氘取代氟的简单方法。所述方法对 FC (sp3 ) 基团具有选择性,并且不影响芳族 FC (sp2 ) 和 F2 -C (sp3 ) 部分。烷基氟化物,通过用二乙氨基三氟化硫 (DAST) 试剂处理,很容易从合适的醇合成,总产率高达 76%,用硼基路易斯酸 B(C6 F5 )3 进行活化,并用三碘化物/氘化物试剂 - 受挫路易斯对的 [TMP2(3) H][2(3) HB(C6 F5 )3 ] 系统。这种方法提供了高达 93% 的区域特异性标记的小有机化合物的分离产率,其 2 H 富集率超过 95%。制备的 1-(2-[3 H]-乙基)萘的比活性测定为 29.0 Ci/mmol。路易斯酸/[TMP2(3) H][2(3) HB(C6 F5 )3 ] 方法的位点选择性与当前使用的方法正交,并允许对分子中的互补位置进行同位素标记。报告的标记方法在超温和反应条件(220 毫巴 T
    DOI:
    10.1002/jlcr.3782
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文献信息

  • gem-Difluorovinyl Derivatives as Insecticides and Acaricides
    作者:Thomas Pitterna、Manfred Böger、Peter Maienfisch
    DOI:10.2533/000942904777678163
    日期:——

    The insecticidal lead 1,1-difluorododec-1-ene was optimised. This compound has attractive insecticidal activity against tobacco budworm (Heliothis virescens), banded cucumber beetle (Diabrotica balteata), pea aphid (Aphis cracciovora), brown planthopper (Nilaparvata lugens), and green rice leafhopper (Nephotettix cincticeps). Among different pharmacophore analogues, only 1,1-dichlorododec-1-ene and 1,1-difluoro-2-iodododec-1-ene showed weak insecticidal activity, whereas similar compounds such as 1-chloro-1-fluorododec-1-ene, 1-fluorododec-1-ene, and 1,1-difluoro-2-bromododec-1-ene were inactive. Only bridge analogues with even-numbered carbon chains were active, for example 1,1-difluorodec-1-ene and 1,1-difluorotetradec-1-ene. Odd-numbered analogues such as 1,1-difluoronon-1-ene, 1,1-difluoroundec-1-ene, 1,1-difluorotridec-1-ene, and 1,1-difluoro-pentadec-1-ene showed no activity. Modification of the tail group led to the analogues 12,12-difluorododec-11-enoic acid and its methyl ester, 12,12-difluorododec-11-en-1-ol, 1,1-difluoro-12-methoxydodec-1-ene, and 12,12-difluorododec-11-enylamine, all of which showed insecticidal activity. 12,12-difluorododec-11-enoic acid methyl ester, 12,12-difluorododec-11-enoic acid, and 12,12-difluorododec-11-en-1-ol were also active against spider mites (Tetranychus ssp). Thus, in a first optimisation cycle, broad activity against insect pests and mites was discovered. Two requirements, the gem-difluorovinyl pharmacophore and an even-numbered carbon chain, were found to be essential for activity. This latter requirement is in line with the proposed mode of action, which involves inhibition of the ? -oxidation of fatty acids in insect mitochondria. In a second optimisation cycle, it was found that 6,6-difluorohex-5-enoic acid and its derivatives, such as acids, amides, and hydrazides, possess even superior properties as insecticides and acaricides. This led to the discovery of 6,6-difluorohex-5-enoic acid 2-[4-(4-trifluoromethylbenzyloxy)-phenoxy]-ethyl ester (CGA 304'111). This compound showed excellent performance in field trials against a wide range of pests, as well as a more favourable toxicological profile than earlier derivatives. For a largescale synthesis of CGA 304'111, five different synthetic routes for 6,6-difluorohex-5-enoic acid were developed. The best route involved radical addition of CBrClF2 to pent-4-enoic acid. Removal of bromine by hydrogenation, elimination of chloride and hydrolysis of the ester concluded this most efficient sequence. Thus, a practical synthesis for CGA 304'111 was identified, which allowed the preparation of samples on a several 100 g scale.

    1,1-二氟十二烯是一种杀虫剂铅化合物,具有对烟草夜蛾、条纹黄瓜甲(Diabrotica balteata)、豌豆蚜虫(Aphis cracciovora)、褐飞虱(Nilaparvata lugens)和绿稻叶蝉(Nephotettix cincticeps)等昆虫的吸引力杀虫活性。在不同的药效团类似物中,只有1,1-二氯十二烯和1,1-二氟-2-碘十二烯表现出微弱的杀虫活性,而类似化合物如1-氯-1-氟十二烯、1-氟十二烯和1,1-二氟-2-溴十二烯则无活性。只有具有偶数碳链的桥接类似物才具有活性,例如1,1-二氟十烯和1,1-二氟十四烯。奇数碳链的类似物如1,1-二氟壬-1-烯、1,1-二氟十一-烯、1,1-二氟十三-烯和1,1-二氟十五-烯均没有活性。修改尾基导致类似物12,12-二氟十二-11-烯酸及其甲酯、12,12-二氟十二-11-烯-1-醇、1,1-二氟-12-甲氧基十二烯和12,12-二氟十二-11-烯基胺,均表现出杀虫活性。12,12-二氟十二-11-烯酸甲酯、12,12-二氟十二-11-烯酸和12,12-二氟十二-11-烯-1-醇也对蜘蛛螨(Tetranychus ssp)具有活性。因此,在第一个优化周期中,发现了对昆虫害虫和螨类广泛活性。两个要求,即gem-二氟乙烯药效团和偶数碳链,被发现是活性所必需的。后一个要求符合所提出的作用模式,涉及对昆虫线粒体中脂肪酸的β-氧化的抑制。在第二个优化周期中,发现6,6-二氟己-5-烯酸及其衍生物,如酸、酰胺和肼,具有更优越的杀虫剂和杀螨剂性能。这导致了6,6-二氟己-5-烯酸2-[4-(4-三氟甲基苄氧基)-苯氧基]-乙酯(CGA 304'111)的发现。这种化合物在田间试验中表现出对多种害虫的优异性能,且毒理学特性比早期衍生物更有利。为了大规模合成CGA 304'111,开发了六种不同的6,6-二氟己-5-烯酸合成路线。最佳路线涉及对戊-4-烯酸进行自由基加成反应。通过氢化去除溴,消除氯并水解酯结束了这个最有效的序列。因此,确定了CGA 304'111的实用合成方法,可以在数百克的规模上制备样品。
  • [EN] LIPOPHILIC ANALOGS OF CJ-16264, METHODS OF USE, AND SYNTHESIS THEREOF<br/>[FR] ANALOGUES LIPOPHILES DE CJ-16264, MÉTHODES D'UTILISATION ET SYNTHÈSE DE CEUX-CI
    申请人:UNIV RICE WILLIAM M
    公开号:WO2017100514A1
    公开(公告)日:2017-06-15
    In one aspect, the present disclosure provides compounds and derivatives of CJ-16,264 of the formula (I) wherein the variables are as defined herein. The application also provides compositions, methods of treatment, and methods of synthesis thereof. In some embodiments, these compounds are used in the treatment of bacterial infections or in the treatment of cancer.
    在一个方面,本公开提供了CJ-16,264的化合物和衍生物,其化学式为(I),其中变量如本文所定义。该申请还提供了组合物、治疗方法以及合成方法。在某些实施例中,这些化合物被用于治疗细菌感染或癌症的治疗。
  • POLYISOCYANATE COMPOSITION AND ISOCYANATE POLYMER COMPOSITION
    申请人:Asahi Kasei Chemicals Corporation
    公开号:EP2915803A1
    公开(公告)日:2015-09-09
    The present invention relates to a polyisocyanate composition comprising, on the basis of the total mass of the polyisocyanate composition, 97 weight % or more of a polyisocyanate, and 2.0 mass ppm or more and 1.0×104 mass ppm or less of a compound having at least one unsaturated bond in which the compound is a different compound from the polyisocyanate, or 5.0 mass ppm or more and 2.0×104 mass ppm or less of at least one inactive compound selected from the group consisting of a hydrocarbon compound, an ether compound, a sulfide compound, a halogenated hydrocarbon compound, a Si-containing hydrocarbon compound, a Si-containing ether compound, and a Si-containing sulfide compound.
    本发明涉及一种多异氰酸酯组合物,以该多异氰酸酯组合物的总质量为基准,该组合物包含 97 重量%或以上的多异氰酸酯,以及 2.0 质量 ppm 或以上且 1.0×104 质量 ppm 或以下的至少具有一个不饱和键的化合物,其中该化合物是与多异氰酸酯不同的化合物,或 5.0 质量 ppm 或以上且 2.0×104 质量 ppm 或以下的至少一种非活性化合物,该化合物选 自烃化合物、醚化合物、硫化物化合物、卤代烃化合物、含硅烃化合物、含硅醚化合物和含硅硫 化物组成的组。
  • ISOCYANATE COMPOSITION, ISOCYANATE POLYMER PRODUCTION METHOD, AND ISOCYANATE POLYMER
    申请人:ASAHI KASEI KABUSHIKI KAISHA
    公开号:EP3527603A1
    公开(公告)日:2019-08-21
    The present invention provides an isocyanate composition including an isocyanate compound having an ethylenically unsaturated bond, a compound represented by formula (1) (in the formula, R1 represents an a-valent organic group, R2 represents a monovalent organic group, a represents an integer of 1 or 2), and/or a compound having a UV absorption in a spectral region of a decamer or higher isocyanate measured by gel permeation chromatography; and an isocyanate composition including an isocyanate compound having an ethylenically unsaturated bond, or a compound having at least one unsaturated bond other than an unsaturated bond constituting an aromatic ring or an inert compound such as a hydrocarbon compound or the like and having a carbon-carbon unsaturated bond other than an unsaturated bond constituting an aromatic ring; or the like.         R1-(COO-R2)a     (1)
    本发明提供了一种异氰酸酯组合物,包括具有乙烯不饱和键的异氰酸酯化合物、由式(1)代表的化合物(式中,R1代表一价有机基团,R2代表一价有机基团,a代表1或2的整数),和/或通过凝胶渗透色谱法测量在十聚体或更高异氰酸酯光谱区具有紫外吸收的化合物;异氰酸酯组合物,包括具有乙烯不饱和键的异氰酸酯化合物,或具有至少一个不饱和键(构成芳香环的不饱和键除外)的化合物,或惰性化合物(如烃类化合物等),且具有碳-碳不饱和键(构成芳香环的不饱和键除外)的化合物;或类似物。 R1-(COO-R2)a (1)
  • ISOCYANATE COMPOSITION AND PRODUCTION METHOD FOR ISOCYANATE POLYMER
    申请人:ASAHI KASEI KABUSHIKI KAISHA
    公开号:EP3527600A1
    公开(公告)日:2019-08-21
    An isocyanate composition according to the present invention contains: a difunctional or more-functional isocyanate compound; and 1.0 ppm by mass to 1.0 × 104 ppm by mass, based on the isocyanate compound, of a compound having at least one unsaturated bond excluding unsaturated bonds constituting an aromatic ring, the compound being different from the isocyanate.
    根据本发明的异氰酸酯组合物含有:双官能团或更多官能团的异氰酸酯化合物;以及以异氰酸酯化合物为基准,质量分数为 1.0 ppm 至 1.0 × 104 ppm 的化合物,该化合物具有至少一个不饱和键,不包括构成芳香环的不饱和键,该化合物不同于异氰酸酯。
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