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Hexanoic acid, 1-carboxyethyl ester | 152433-76-6

中文名称
——
中文别名
——
英文名称
Hexanoic acid, 1-carboxyethyl ester
英文别名
2-hexanoyloxypropanoic acid
Hexanoic acid, 1-carboxyethyl ester化学式
CAS
152433-76-6
化学式
C9H16O4
mdl
——
分子量
188.22
InChiKey
BTKPZBXSSYHWRT-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
  • 重原子数:
    13
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    63.6
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • [EN] PROCESS FOR MAKING ESTERS OF 2-ACETOXYALKANOIC ACIDS USING A 3,6-DIALKYL-1,4-DIOXANE-2,5-DIONE OR POLY-(ALPHA-HYDROXYALKANOIC ACID) AS A STARTING MATERIAL<br/>[FR] PROCEDE DE FABRICATION D'ESTERS D'ACIDES 2-ACETOXYALCANOIQUES UTILISANT LE COMPOSE 3,6-DIALKYL-1,4-DIOXANE-2,5-DIONE OU POLY(ACIDE ALPHA-HYDROXYALCANOIQUE) EN TANT QUE MATIERE PREMIERE
    申请人:NATUREWORKS LLC
    公开号:WO2015127374A1
    公开(公告)日:2015-08-27
    2-Acetoxyalkanoic acid esters are made in a reaction of a 3,6-dialkyl-1,4-dioxane-2,5-dione or a poly(α-hydroxyalkanoic acid), an acetate ester and an alcohol or phenol in the presence of a transesterification catalyst. Unlike previous methods for making 2-acetoxyalkanoic acid esters, this process proceeds in high yield and high selectivity to the desired product.
    2-乙酰氧基烷酸酯是通过在3,6-二烷基-1,4-二氧杂环戊二酮或聚(α-羟基烷酸)、醋酸酯和醇或的反应中,在酯交换催化剂的存在下制备的。与以往制备2-乙酰氧基烷酸酯的方法不同,这个过程产率高,对所需产品选择性高。
  • [EN] PROCESS FOR MAKING ESTERS OF 2-ACETOXYALKANOIC ACIDS USING AN ALPHA-HYDROXYALKANOIC ACID ESTER AND AN ACETATE ESTER AS STARTING MATERIALS<br/>[FR] PROCÉDÉ DE PRODUCTION D'ESTERS D'ACIDES 2-ACÉTOXYALCANOÏQUES UTILISANT UN ESTER D'ACIDE ALPHA-HYDROXYALCANOÏQUE ET UN ESTER D'ACÉTATE EN TANT QUE MATÉRIAUX DE DÉPART
    申请人:NATURE WORKS LLC
    公开号:WO2015127372A1
    公开(公告)日:2015-08-27
    2-Acetoxyalkanoic acid esters are made in a reaction of an α-hydroxyalkanoic acid ester and an acetate ester in the presence of a transesterification catalyst. Unlike previous methods for making 2-acetoxyalkanoic acid esters, this process proceeds in high yield and high selectivity to the desired product.
    2-乙酰氧基烷酸酯是由α-羟基烷酸酯和醋酸酯在转酯催化剂存在下反应制得的。与以往制备2-乙酰氧基烷酸酯的方法不同,这个过程产率高,对所需产品具有高选择性。
  • PROCESS FOR MAKING A 2-ACETOXYALKANOIC ESTER
    申请人:NatureWorks LLC
    公开号:EP3333148A1
    公开(公告)日:2018-06-13
    2-Acetoxyalkanoic acid esters are made in a reaction of a poly(α-hydroxyalkanoic acid), an acetate ester and an alcohol or phenol in the presence of a transesterification catalyst. Unlike previous methods for making 2-acetoxyalkanoic acid esters, this process proceeds in high yield and high selectivity to the desired product.
    2- 乙酰氧基烷酸酯是由聚(α-羟基烷酸)、乙酸酯和醇或苯酚在酯交换催化剂的作用下反应制成的。与以往制造 2-乙酰氧基烷酸酯的方法不同,这种工艺能以高产率和高选择性获得所需的产品。
  • Process for making esters of 2-acetoxyalkanoic acids using an α-hydroxyalkanoic acid ester and an acetate ester as starting materials
    申请人:NatureWorks LLC
    公开号:US10294188B2
    公开(公告)日:2019-05-21
    2-Acetoxyalkanoic acid esters are made in a reaction of an α-hydroxyalkanoic acid ester and an acetate ester in the presence of a transesterification catalyst. Unlike previous methods for making 2-acetoxyalkanoic acid esters, this process proceeds in high yield and high selectivity to the desired product.
    2- 乙酰氧基烷酸酯是由α-羟基烷酸酯和乙酸酯在酯交换催化剂作用下反应生成的。与以往制造 2-乙酰氧基烷酸酯的方法不同,这种工艺能以高产率和高选择性获得所需的产品。
  • Process for making esters of 2-acetoxyalkanoic acids using a 3,6-dialkyl-1,4-dioxane-2,5-dione or poly-(alpha-hydroxyalkanoic acid) as a starting material
    申请人:NatureWorks LLC
    公开号:US10385002B2
    公开(公告)日:2019-08-20
    2-Acetoxyalkanoic acid esters are made in a reaction of a 3,6-dialkyl-1,4-dioxane-2,5-dione or a poly(α-hydroxyalkanoic acid), an acetate ester and an alcohol or phenol in the presence of a transesterification catalyst. Unlike previous methods for making 2-acetoxyalkanoic acid esters, this process proceeds in high yield and high selectivity to the desired product.
    2- 乙酰氧基烷酸酯是由 3,6-二烷基-1,4-二氧六环-2,5-二酮或聚(α-羟基烷酸)、乙酸酯和醇或苯酚在酯交换催化剂存在下反应制成的。与以往制造 2-乙酰氧基烷酸酯的方法不同,这种工艺能以高产率和高选择性获得所需的产品。
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