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2-Methyl-3-(1-methylethoxy)-1-propanol | 53892-31-2

中文名称
——
中文别名
——
英文名称
2-Methyl-3-(1-methylethoxy)-1-propanol
英文别名
2-methyl-3-propan-2-yloxypropan-1-ol
2-Methyl-3-(1-methylethoxy)-1-propanol化学式
CAS
53892-31-2
化学式
C7H16O2
mdl
——
分子量
132.2
InChiKey
FISVCANEQCZAML-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):
    1
  • 重原子数:
    9
  • 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:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • COMPOUND CONTAINING PYRIDINE RING AND METHOD FOR PRODUCING HALOGENATED PICOLINE DERIVATIVE AND TETRAZOLYLOXIME DERIVATIVE
    申请人:Miyazaki Hidekazu
    公开号:US20130012713A1
    公开(公告)日:2013-01-10
    Disclosed is a compound containing a pyridine ring that can be synthesized in an industrially advantageous manner, and is useful as an intermediate for producing tetrazolyloxime derivatives that exhibit fungicidal activity (wherein R 0 represents a C 1-6 alkoxy group, C 1-6 alkoxy-C 1-6 alkoxy group or the like, R 1 represents a C 1-2 alkoxycarbonyl group, acetyl group or the like, Z represents a halogen atom, cyano group or the like, X represents a halogen atom, and n represents an integer of 0 to 3), and industrially advantageous production methods for producing 2-substituted amino-6-halomethylpyridine derivatives and tetrazolyloxime derivatives.
    本发明公开了一种含有吡啶环的化合物,可以以工业上有利的方式合成,并且可用作生产具有杀真菌活性的四唑氧肟衍生物的中间体(其中R0代表C1-6烷氧基基团,C1-6烷氧基-C1-6烷氧基基团或类似物,R1代表C1-2烷氧羰基基团,乙酰基基团或类似物,Z代表卤素原子,氰基团或类似物,X代表卤素原子,n代表0至3的整数),以及用于生产2-取代氨基-6-卤甲基吡啶衍生物和四唑氧肟衍生物的工业上有利的生产方法。
  • [EN] METHOD FOR PREPARATION OF CERTAIN 1,5 DISUBSTITUTED TETRAZOLES<br/>[FR] PROCÉDÉ DE PRÉPARATION DE CERTAINS TÉTRAZOLES 1,5 DISUBSTITUÉS
    申请人:LONZA AG
    公开号:WO2016142364A1
    公开(公告)日:2016-09-15
    The invention discloses a method for the preparation of certain 1,5 disubstituted tetrazole and similar compounds starting from certain thioacetamides, which ultimately allows the preparation of these certain 1,5 disubstituted tetrazoles from readily available compounds such as acetophenone and similar compounds.
    该发明揭示了一种从某些硫代乙酰胺起始制备某些1,5-二取代四唑和类似化合物的方法,最终允许从可轻易获得的化合物(如苯乙酮和类似化合物)制备这些某些1,5-二取代四唑。
  • Process to halogenate a picoline derivative
    申请人:NIPPON SODA CO., LTD.
    公开号:EP2719686A1
    公开(公告)日:2014-04-16
    Disclosed is a process to halogenate compounds (2) to produce compounds (3).
    本发明公开了一种卤化化合物 (2) 以生成化合物 (3) 的工艺。
  • Process for producing tetrazolyloxime derivatives
    申请人:NIPPON SODA CO., LTD.
    公开号:EP2719688A1
    公开(公告)日:2014-04-16
    Method for producing a tetrazolyloxime derivative represented by formula (10), the method comprising: a step C1 in which a hologenated picoline derivative represented by formula (7) is reacted with a tetrazolylhydroxyimino derivative represented by formula (8) to obtain a tetrazolyloxime derivative represented by formula (9); and a step C2 in which the tetrazolyloxime derivative reperesented by formula (9) obtained in the step C1 is treated with a base, The compounds (9) are also claimed.
    生产式(10)代表的四唑肟衍生物的方法,该方法包括:步骤 C1,在该步骤中,式(7)代表的全息化皮啶衍生物与式(8)代表的四唑羟基亚氨基衍生物反应,得到式(9)代表的四唑肟衍生物;以及步骤 C2,在该步骤中,用碱处理在步骤 C1 中得到的由式(9)再代表的四唑肟衍生物、 还要求得到化合物(9)。
  • METHOD FOR PREPARATION OF CERTAIN THIOACETAMIDES
    申请人:Lonza Ltd
    公开号:EP3112344A1
    公开(公告)日:2017-01-04
    The invention discloses a method for the preparation of certain thioacetamides with sulfur chlorides starting from certain methylketones, and their use in the preparation of certain 1,5 disubstituted tetrazoles, which allows the preparation of said tetrazoles from readily available compounds such as acetophenone and similar compounds.
    本发明公开了一种以某些甲基酮为起点,用硫酰氯制备某些硫代乙酰胺的方法,以及将其用于制备某些 1,5 二取代四唑的方法,该方法可以用苯乙酮和类似化合物等容易获得的化合物制备上述四唑。
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