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bis(2,3-dichloro-1-propyl) ether | 651059-68-6

中文名称
——
中文别名
——
英文名称
bis(2,3-dichloro-1-propyl) ether
英文别名
dichloroisopropyl ether;1,2-Dichloro-2-[(1,2-dichloropropan-2-yl)oxy]propane;1,2-dichloro-2-(1,2-dichloropropan-2-yloxy)propane
bis(2,3-dichloro-1-propyl) ether化学式
CAS
651059-68-6
化学式
C6H10Cl4O
mdl
——
分子量
239.957
InChiKey
WZKYSMVCTDJJAR-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    11
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • CARBOXY ESTER KETALS, METHODS OF MANUFACTURE, AND USES THEREOF
    申请人:SEGETIS, INC.
    公开号:US20140147395A1
    公开(公告)日:2014-05-29
    This disclosure is directed to compound of formula (1): wherein R 1 is a C 7-18 alkyl, R 2 is hydrogen or a C 1-3 alkyl, each R 3 , R 4 , R 5 , R 6 , and R 7 is independently hydrogen or a C 1-6 alkyl, a is 2-3, and b is 0-1, its method of preparation and uses thereof in water-borne coating compositions, cleaning compositions, fragrance, and personal care compositions.
    这项披露涉及到化合物的结构式(1):其中R1是C7-18烷基,R2是氢或C1-3烷基,每个R3、R4、R5、R6和R7独立地是氢或C1-6烷基,a为2-3,b为0-1,以及其在水性涂料组合物、清洁组合物、香料和个人护理组合物中的制备方法和用途。
  • [EN] PROCESS FOR HYDROGENATING DICHLOROISOPROPYL ETHER<br/>[FR] PROCÉDÉ D'HYDROGÉNATION D'ÉTHER DE DICHLOROISOPROPYLE
    申请人:DOW GLOBAL TECHNOLOGIES LLC
    公开号:WO2016044009A1
    公开(公告)日:2016-03-24
    Convert dichloroisopropyl ether into a halogenated derivative by contacting the dichloroisopropyl ether with a source of hydrogen and a select heterogeneous hydrogenation catalyst under process conditions selected from a combination of a temperature within a range of from 50 degrees centigrade (ºC) to 350 ºC, a pressure within a range of from atmospheric pressure (0.1 megapascals) to 1000 pounds per square inch (6.9 MPa), a liquid feed volume flow to catalyst mass ratio between 0.5 and 10 L/Kg*h and a volume hydrogen / volume liquid ratio between 100 and 5000 ml gas/ ml liquid. The halogenated derivative is at least one of 1-chloro-2-propanol and 1,2-dichloropropane 1, and glycerin monochlorohydrin.
    通过将二氯异丙醚与氢源和选择性的杂化氢化催化剂接触,在从以下过程条件的组合中选择的条件下,将二氯异丙醚转化为卤代衍生物:温度在50摄氏度(ºC)至350ºC范围内,压力在大气压(0.1兆帕)至1000磅每平方英寸(6.9兆帕)范围内,液体进料体积流量与催化剂质量之比在0.5至10 L/Kg*h之间,氢气体积/液体体积比在100至5000 ml气体/ ml液体之间。卤代衍生物至少为1-氯-2-丙醇和1,2-二氯丙烷1,以及甘油单氯水合物。
  • 5A5B6C Tricyclic spirolactone derivative, preparation method therefor and use thereof
    申请人:NANKAI UNIVERSITY
    公开号:US20210289783A1
    公开(公告)日:2021-09-23
    A 5 A 5 B 6 C tricyclic spironolactone derivative is provided with a formula XI: The present invention also relates to its preparation method and its applications in the areas of insecticide, nematicide, fungicide and anti-viral agent. The 5 A 5 B 6 C tricyclic spironolactone derivatives in the present invention are high-performance, broad-spectrum, low-toxicity and low-ecological risk compounds with a wide range of applications in the areas of agriculture, horticulture, forestry and health.
    本发明提供了一种具有XI式的5A5B6环三环螺内酯衍生物。本发明还涉及其制备方法以及在杀虫剂、线虫杀剂、杀菌剂和抗病毒剂领域的应用。本发明中的5A5B6环三环螺内酯衍生物是高性能、广谱、低毒性和低生态风险化合物,具有广泛的应用范围,可用于农业、园艺、林业和健康领域。
  • METHODS FOR PRODUCING SOLVENTS DERIVED FROM 1-CHLORO-3, 3, 3-TRIFLUORO-PROPENE (1233ZD)
    申请人:Honeywell International Inc.
    公开号:US20170349519A1
    公开(公告)日:2017-12-07
    The production of solvents for applications such as heat transfer, cleaning, and degreasing, for example. In particular, the production of solvents derived from 1-chloro-3,3,3-trifluoro-propene, such as chloro and/or fluoro substituted alkanes and chloro and/or fluoro substituted trifluoropropenyl ethers.
    生产溶剂,用于热传递、清洗和脱脂等应用,例如。特别是生产源自1-氯-3,3,3-三氟丙烯的溶剂,如氯和/或氟取代的烷烃和氯和/或氟取代的三氟丙烯基醚。
  • Process for the production of aminophenols
    申请人:SUMITOMO CHEMICAL COMPANY, LIMITED
    公开号:EP0168976A1
    公开(公告)日:1986-01-22
    @ A divalent phenol is reacted with ammonia without a catalyst or using a water-soluble catalyst, and a product containing an aminophenol and unreacted divalent phenol separated and recovered. The product is then contacted with an aliphatic ether substantially incompatible with said aminophenol in an inert gas atmosphere at its melting point or a higher temperature, and the resultant mixture then cooled to induce crystallization of the aminophenol, and thereafter filtered to obtain a cake mainly composed of said aminophenol. The cake is melted and contacted with an aliphatic ether in an inert gas atmosphere in the co-presence of water and a surfactant, and the resultant mixture cooled to crystallize the aminophenol, which is finally recovered.
    二价酚在没有催化剂或使用水溶性催化剂的情况下与氨反应,分离并回收含有氨基苯酚和未反应二价酚的产物。然后,在惰性气体环境中,在氨基苯酚的熔点或更高温度下,将该产物与基本上与氨基苯酚不相容的脂肪族醚接触,然后冷却所得到的混合物,促使氨基苯酚结晶,之后过滤,得到主要由氨基苯酚组成的滤饼。在惰性气体环境中,在水和表面活性剂的共同作用下,将滤饼熔化并与脂肪族醚接触,然后冷却所得混合物,使氨基苯酚结晶,最后将其回收。
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