acetic acid-(1-isopropyl-pentyl ester) | 116496-84-5

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: acetic acid-(1-isopropyl-pentyl ester)
• 英文别名: Essigsaeure-(1-isopropyl-pentylester)；Acetic acid 1-isopropyl-pentyl ester；2-methylheptan-3-yl acetate
• CAS: 116496-84-5
• 化学式: C₁₀H₂₀O₂
• mdl: MFCD00049103
• 分子量: 172.268
• InChiKey: MOAHBTJSRYNEIB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  12
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2-甲基-3-庚醇 、 乙酰氯 生成 acetic acid-(1-isopropyl-pentyl ester)
  参考文献：
  名称：

  Muset, Chemisches Zentralblatt, 1907, vol. 78, # I, p. 1313

  摘要：

  DOI：

文献信息

• IMPROVED MEDICAL DEVICE HAVING DESIRABLE COMBINATION OF PROPERTIES AND METHOD OF MAKING SAME
  申请人：Medtronic AVE, Inc.

  公开号：EP0983097A1

  公开（公告）日：2000-03-08
• [EN] IMPROVED MEDICAL DEVICE HAVING DESIRABLE COMBINATION OF PROPERTIES AND METHOD OF MAKING SAME<br/>[FR] DISPOSITIF MEDICAL AMELIORE PRESENTANT UNE COMBINAISON DE PROPRIETES VOULUES, ET SON PROCEDE DE FABRICATION
  申请人：MEDTRONIC AVE,INC.

  公开号：WO1998050087A1

  公开（公告）日：1998-11-12

  (EN) This invention relates to coated medical devices adapted to pass through narrow body openings such as catheters. The coatings provided by this invention impart durability to the catheter without appreciably adding to the thickness of the catheter and without decreasing the hoop tensile strength of the catheter.(FR) L'invention a trait à des dispositifs médicaux revêtus, conçus pour passer à travers des ouvertures de corps étroits, tels que des cathéters. Les revêtements prévus par l'invention confèrent une durabilité au cathéter sans accroître de façon appréciable l'épaisseur du cathéter, et sans réduire la résistance à la traction périphérique du cathéter.
• [EN] METHOD OF PRODUCING ACETOXYARYL CARBOXYLIC ACIDS<br/>[FR] PROCEDE DE PRODUCTION D'ACIDES CARBOXYLIQUES D'ACETOXYARYLE
  申请人：EASTMAN CHEM CO

  公开号：WO2000027787A1

  公开（公告）日：2000-05-18

  A method of producing an acetoxyaryl carboxylic acid converts a dialkylaryl to a monohydroperoxide of the dialkylaryl, converts the monohydroperoxide of the dialkylaryl to an alkylaryl acetate, and oxidizes the alkylaryl acetate to the acetoxyaryl carboxylic acid in the presence of cobalt and bromine catalysts. If the alkyl groups are isopropyl groups, the method converts a monohydroperoxide of a diisopropylaryl to an isopropylaryl acetate and oxidizes the isopropylaryl acetate to the acetoxyaryl carboxylic acid in the presence of cobalt and bromine catalysts. Alternatively, it is possible to produce the acetoxyaryl carboxylic acid from an isopropylaryl alcohol. In this case, the isopropylaryl alcohol is converted to an isopropylaryl acetate and the isopropylaryl acetate is oxidized to the acetoxyaryl carboxylic acid in the presence of cobalt and bromine catalysts. The isopropylaryl acetate may be isolated prior to the oxidation step. Alternatively, the isopropylaryl acetate may not be isolated prior to the oxidation substep. However, acetone is produced in the step of converting the monohydroperoxide of the diisopropylaryl to the isopropylaryl acetate, and the acetone should be removed prior to the oxidation step. The aryl group may be a phenyl group or a naphthyl group. The oxidation step may be conducted in the presence of cobalt, bromine and manganese catalysts and more preferably in the presence of cobalt, bromine, manganese and potassium catalysts. The cobalt concentration should be within the range of from 0.01 molar to 0.05 molar and more preferably within the range of from 0.02 molar to 0.03 molar.