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methyl 2-(2-chloroacetoxy)benzoate | 60504-02-1

中文名称
——
中文别名
——
英文名称
methyl 2-(2-chloroacetoxy)benzoate
英文别名
Chloressigsaeure-(2-methoxycarbonyl-phenylester);2-chloroacetoxy-benzoic acid methyl ester;2-Chloracetoxy-benzoesaeure-methylester;Chloracetyl-salicylsaeuremethylester;Methyl 2-[(chloroacetyl)oxy]benzoate;methyl 2-(2-chloroacetyl)oxybenzoate
methyl 2-(2-chloroacetoxy)benzoate化学式
CAS
60504-02-1
化学式
C10H9ClO4
mdl
——
分子量
228.632
InChiKey
BOMYQMNIRPEDGO-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):
    2.1
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:02595333dc91b64db4d5476ba9fe7b85
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    methyl 2-(2-chloroacetoxy)benzoate丙酮 、 sodium iodide 作用下, 生成 2-pyrrolidinoacetoxy-benzoic acid methyl ester; hydrochloride
    参考文献:
    名称:
    Reactions in the Salicylic Acid Series. A New Rearrangement of Acylsalicylic Acid Derivatives
    摘要:
    DOI:
    10.1021/ja01517a050
  • 作为产物:
    描述:
    氯乙酰氯水杨酸甲酯三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 8.0h, 以56%的产率得到methyl 2-(2-chloroacetoxy)benzoate
    参考文献:
    名称:
    Mali, Raghao S.; Deshpande, Jyoti V., Organic Preparations and Procedures International, 1995, vol. 27, # 6, p. 663 - 667
    摘要:
    DOI:
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文献信息

  • Hahn; Loos, Chemische Berichte, 1918, vol. 51, p. 1442
    作者:Hahn、Loos
    DOI:——
    日期:——
  • Reduction of Substituted Phenyl 2-Chloroacetates at Silver Cathodes: Electrosynthesis of Coumarins
    作者:Erick M. Pasciak、Dennis G. Peters
    DOI:10.1149/2.0551412jes
    日期:——
    To explore the electrosynthesis of coumarins, cyclic voltammetry and controlled-potential (bulk) electrolysis have been employed to investigate the reduction of the carbon-chlorine bond of five substituted phenyl 2-chloroacetates at silver cathodes in dimethylformamide (DMF) containing 0.10 M tetra-n-butylammonium tetrafluoroborate (TBABF(4)) as supporting electrolyte; the five substrates are 2-formylphenyl 2-chloroacetate (1a), 2-acetylphenyl 2-chloroacetate (2a), methyl 2-(2-chloroacetoxy)benzoate (3a), 2-formyl-5-methoxyphenyl 2-chloroacetate (4a), and 2-formyl-3,5-dimethoxyphenyl 2-chloroacetate (5a). We have examined (a) the effects of substituents on the benzene ring of the substrate as well as the nature of the aryl carbonyl moiety on the formation of the coumarin product and (b) the effect of solvent-namely, DMF, acetonitrile (CH3CN), benzonitrile (PhCN), and propylene carbonate (PC)-and substrate concentration on the yield of the coumarin. It was found that the most unsubstituted substrate (1a) afforded the highest yield (41%) of the desired coumarin in a DMF-TBABF(4) medium. A mechanistic scheme is proposed to account for the formation of the coumarin. Furthermore, the only other products seen in these reductions are 2-substituted phenols, which are precursors for synthesis of the various substrates. (C) 2014 The Electrochemical Society. All rights reserved.
  • FILM-FORMING POLYMER AND ANTIFOULING PAINT
    申请人:Jotun AS
    公开号:EP1487928A1
    公开(公告)日:2004-12-22
  • US4835312A
    申请人:——
    公开号:US4835312A
    公开(公告)日:1989-05-30
  • [EN] FILM-FORMING POLYMER AND ANTIFOULING PAINT<br/>[FR] POLYMERE FILMOGENE ET PEINTURE ANTISALISSURE
    申请人:JOTUN AS
    公开号:WO2003080747A1
    公开(公告)日:2003-10-02
    Water insoluble, water erodible, film forming polymer for antifouling paint, which includes repeating units corresponding to the monomers A and B : A) 2-95 mole % of monomers of formula (I), wherein n is an integer from 1 to 4, X is H or CH3, Y is H or an optionally esterified COOH group, R1 is Ph(R2)m, -C(O)R3 or -Si(R4)3, m is an integer from 1 to 3, R2, which are the same or different, are selected from -C(O)H, C(O)R5, COOR6, CH2COOR7, C1-4 alkyl, C1-4 alkanoyl, halogen, nitro, OH and OR8, R3 is selected from substituted or unsubstituted alkyl, aryl, aralkyl and heterocyclyl, R4, which are the same or different, are selected from substituted or unsubstituted C1-20 alkyl, C5-20 aryl, C1-20 alkoxy and C5-20 aryloxy, and R5, R6, R7 and R8 are independently selected from substituted or unsubstituted C1-20 alkyl and C5-20 aryl; and B) 5-98 mole % of other vinyl polymerisable monomers.
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