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4-bromo-4-(2,2,2-trichloroethyl)oxetan-2-one | 81189-94-8

中文名称
——
中文别名
——
英文名称
4-bromo-4-(2,2,2-trichloroethyl)oxetan-2-one
英文别名
4-Bromo-4-(2,2,2-trichloroethyl)-oxetan-2-one
4-bromo-4-(2,2,2-trichloroethyl)oxetan-2-one化学式
CAS
81189-94-8
化学式
C5H4BrCl3O2
mdl
——
分子量
282.349
InChiKey
IAUUXUPPUOCYTN-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

  • 熔点:
    54-55 °C(Solv: ligroine (8032-32-4))
  • 沸点:
    314.1±42.0 °C(Predicted)
  • 密度:
    1.973±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • 4-Halgeno-oxetan-2-ones and process for their production
    申请人:Ciba-Geigy Corporation
    公开号:US04363923A1
    公开(公告)日:1982-12-14
    Novel compounds having the formula I ##STR1## are described wherein X is a chlorine, bromine or iodine atom and Y is a residue having the formula R.sup.1 R.sup.2 R.sup.3 C- wherein R.sup.1 and R.sup.2 are the same or different and each is a fluorine, chlorine or bromine atom and R.sup.3 is a hydrogen, fluorine, chlorine or bromine atom, a group -CR.sup.4 R.sup.5 R.sup.6, a cyano group, a group-COR.sup.7 or -PO(R.sup.8).sub.2 wherein R.sup.4, R.sup.5, R.sup.6, independently, are F, Cl or Br, R.sup.7 nd R.sup.8 are the same or different and each is a chlorine atom or a group -OR.sup.9 wherein R.sup.9 is a C.sub.1 -C.sub.4 straight chain or branched alkyl group with the proviso that when X is a chlorine atom, none of R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5 and R.sup.6, can be a bromine atom. They can be obtained by reacting diketene with a compound XY in the presence of an agent capable of forming free radicals. Compounds (I) have biocidal activity against various organisms, e.g. bacteria, fungi and algae.
    本发明描述了具有公式I的新化合物,其中X是氯、溴或碘原子,Y是具有公式R.sup.1 R.sup.2 R.sup.3 C-的残基,其中R.sup.1和R.sup.2相同或不同,且每个都是氟、氯或溴原子,R.sup.3是氢、氟、氯或溴原子、-CR.sup.4 R.sup.5 R.sup.6基团、氰基、-COR.sup.7或-PO(R.sup.8).sub.2,其中R.sup.4、R.sup.5、R.sup.6独立地是F、Cl或Br,R.sup.7和R.sup.8相同或不同,每个都是氯原子或-OR.sup.9基团,其中R.sup.9是C.sub.1-C.sub.4直链或支链烷基,但当X是氯原子时,R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5和R.sup.6中没有一个可以是溴原子。它们可以通过在能够形成自由基的剂的存在下,将二酮与化合物XY反应而得到。化合物(I)对各种生物具有生物杀灭活性,例如细菌、真菌和藻类。
  • Production of 5,5-disubstituted 3-oxo-pent-4-enoic acids, their halides, esters, thioesters and amides; and their use in antifungal and antibacterial compositions
    申请人:CIBA-GEIGY AG
    公开号:EP0067124A1
    公开(公告)日:1982-12-15
    A process is described for the production of a compound having the formula: R2R2C=CHCOCH2COZ I wherein R2 is fluorine, chlorine, or. bromine; R3 is hydrogen, fluorine, chlorine or bromine, or a group of formula -CR4R5R6 wherein R4, R5 and R6 are fluorine, chlorine or bromine; and Z is -AY or X1 wherein A is -O-, -S- or -NR7 wherein R7 is hydrogen, C1-10- straight - or branch chain alkyl or C3-4 straight or branch chain alkenyl, Y is hydrogen, C 1-18-straight or branch chain alkyl optionally interrrupted by one to five oxygen atoms and optionally substituted by one to five chlorine or bromine atoms, or by a group having the formula -OR8 or the formula -CO2R9 wherein R8 is hydrogen, C3-12-cycloalkyl, straight- or branch chain C3-18- alkenyl, C6-10-aryl or C7-13-aralkyl and R9 is hydrogen, C1-18- straight- or branch chain alkyl or straight- or branch chain C3-18- alkenyl, or Y is C3-18 straight or branch chain alkenyl, C3-18 straight- or branch chain alkynyl, C3-12-cycloalkyl, C7-13-aralkyl, or C6-10- aryl which is optionally substituted by one to three C1-9 straigth- or branch chain alkyl, halogen, nitro, CF3, or SO3H, or groups -OR10 wherein R10 is hydrogen or C1-4 straight or branch chain alkyl, provided that the total number of carbon atoms in the group -AY is from 0 to 20; or R7 and Y together may form a C2-7 polymethylene chain optionally substituted by one or two C1-4 alkyl groups and optionally interrupted by -0-, -S- or NR11 groups wherein R11 is C1-4 straight or branch chain alkyl; and X1 is C1 or Br; comprising (a) reacting, optionally in the presence of a solvent and an inorganic or organic acid - binding agent, a compound having the formula II: wherein R2 and R3 have their previous significance; R1 is fluorine, chlorine or bromine; and X is chlorine, bromine or iodine with the proviso that, when X is chlorine, none of R1, R2, R3, R4, R5 and R6 can be bromine; with a compound of formula H-Z III wherein Z has its previous significance; and (b) when Z is -AY and -AY is -OH, the product of step a) is optionally reacted with a compound IV capable of converting a carboxyl group into the corresponding carboxylic acid chloride or -bromide, thereby producing a compound of formula I wherein Z is- X1 as well as the use of the compounds of formula I in antifungal and antibacterial compositions.
    描述了一种具有以下式子的化合物的生产工艺:R2R2C=CHCOCH2COZ I 其中 R2 是氟、氯或溴;R3 是氢、氟、氯或溴,或式溴;R3 是氢、氟、氯或溴,或式 -CR4R5R6 的基团,其中 R4、R5 和 R6 是氟、氯或溴;Z是-AY或X1,其中A是-O-、-S-或-NR7,其中R7是氢、C1-10-直链或支链烷基或C3-4直链或支链烯基;Y是氢、C 1-18-直链或支链烷基,可选择被1-5个氧原子间断,并可选择被1-5个氯或溴原子取代、或具有式 -OR8 或式 -CO2R9 的基团,其中 R8 为氢、C3-12-环烷基、C3-18-直链或支链烯基、C6-10-芳基或 C7-13- 芳基,R9 为氢、C1-18 直链或支链烷基或 C3-18 直链或支链烯基,或 Y 是 C3-18 直链或支链烯基、C3-18 直链或支链炔基、C3-12-环烷基、C7-13-芳基、或 C6-10- 芳基,其任选被一至三个 C1-9 直链或支链烷基、卤素、硝基、CF3 或 SO3H 或基团 -OR10 取代,其中 R10 为氢或 C1-4 直链或支链烷基,条件是基团 -AY 中的碳原子总数为 0 至 20;或 R7 和 Y 一起可形成 C2-7 聚亚甲基链,该链可任选被一个或两个 C1-4 烷基取代,并可任选被-0-、-S-或 NR11 基团间断,其中 R11 为 C1-4 直链或支链烷基;以及 X1 为 C1 或 Br;包括 (a) 任选在溶剂和无机或有机酸结合剂存在下,使具有式 II: 其中 R2 和 R3 具有前述意义;R1 是氟、氯或溴;X 是氯、溴或碘,但当 X 是氯时,R1、R2、R3、R4、R5 和 R6 中不能有溴;(b) 当 Z 为-AY 且-AY 为-OH 时,步骤 a)的产物可选择与能将羧基转化为相应的羧酸氯化物或溴化物的化合物 IV 反应,从而生成式 I 化合物(其中 Z 为-X1)以及式 I 化合物在抗真菌和抗菌组合物中的用途。
  • DINGWALL J. G.; TUCK B., J. CHEM. SOC. PERKIN TRANS.,(1986) N 12, 2081-2090
    作者:DINGWALL J. G.、 TUCK B.
    DOI:——
    日期:——
  • US4363923A
    申请人:——
    公开号:US4363923A
    公开(公告)日:1982-12-14
  • Dingwall, John G.; Tuck, Brian, Journal of the Chemical Society. Perkin transactions I, 1986, p. 2081 - 2090
    作者:Dingwall, John G.、Tuck, Brian
    DOI:——
    日期:——
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