1-propoxy-propan-2-one | 68058-77-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-propoxy-propan-2-one
• 英文别名: propoxy-acetone；Propylacetonylaether；Propyloxyaceton；Propoxy-aceton；Acetol-n-propylaether；n-propoxy-2-propanone；2-Propanone, 1-propoxy-；1-propoxypropan-2-one
• CAS: 68058-77-5
• 化学式: C₆H₁₂O₂
• 分子量: 116.16
• InChiKey: XDUMOUTWQVQHII-UHFFFAOYSA-N

物化性质

• 沸点：
  150 °C(Press: 763 Torr)
• 密度：
  0.886±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  8
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.83
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-propoxy-propan-2-one 生成 propoxy-acetone-phenylhydrazone
  参考文献：
  名称：

  Petrow, Zhurnal Obshchei Khimii, 1946, vol. 16, p. 1206,1208, 1209

  摘要：

  DOI：
• 作为产物：
  描述：

  1-丙氧基-2-丙醇 在 sodium dichromate 、 硫酸 作用下， 生成 1-propoxy-propan-2-one
  参考文献：
  名称：

  Petrow, Zhurnal Obshchei Khimii, 1946, vol. 16, p. 1206,1208, 1209

  摘要：

  DOI：

文献信息

• RENIN INHIBITORS
  申请人：Jones Benjamin

  公开号：US20100210635A1

  公开（公告）日：2010-08-19

  Compounds, pharmaceutical compositions, kits and methods are provided for use with Renin that comprise a compound selected from the group consisting of: wherein the variables are as defined herein.

  提供了用于与Renin一起使用的化合物、药物组合物、试剂盒和方法，其中包括从以下组中选择的化合物：其中变量如本文所定义。
• MOLECULAR PRECURSOR COMPOUNDS FOR ZINC-GROUP 13 MIXED OXIDE MATERIALS
  申请人：Precursor Energetics, Inc.

  公开号：US20150218190A1

  公开（公告）日：2015-08-06

  Molecular precursor compounds, processes and compositions for making Zn-Group 13 mixed oxide materials including IZO, GZO, AZO and BZO, by providing inks comprising a molecular precursor compound having the formula M A a Zn(OROR) 3a+2 , and printing or depositing the inks on a substrate. The printed or deposited ink films can be treated to convert the molecular precursor compounds to a material.

  分子前体化合物、制备Zn-Group 13混合氧化物材料（包括IZO、GZO、AZO和BZO）的过程和组合物，方法是提供包含具有公式M的分子前体化合物的油墨，在基底上印刷或沉积这些油墨。印刷或沉积的油墨膜可以经处理转化为材料。
• CONJUGATES COMPRISING HYDROXYALKYL STARCH AND A CYTOTOXIC AGENT AND PROCESS FOR THEIR PREPARATION
  申请人：Fresenius Kabi Deutschland GmbH

  公开号：US20150297738A1

  公开（公告）日：2015-10-22

  The present invention relates to a hydroxyalkyl starch conjugate and a method for preparing the same, said hydroxyalkyl starch conjugate comprising a hydroxyalkyl starch derivative and a cytotoxic agent, the cytotoxic agent comprising at least one secondary hydroxyl group, wherein the hydroxyalkyl starch is linked via said secondary hydroxyl group to the cytotoxic agent. The conjugate according to the present invention has a structure according to the following formula HAS′(-L-M) n wherein M is a residue of the cytotoxic agent, L is a linking moiety, HAS′ is the residue of the hydroxyalkyl starch derivative, and n is greater than or equal to 1, and wherein the hydroxyalkyl starch derivative has a mean molecular weight (MW) above the renal threshold.

  本发明涉及一种羟烷基淀粉共轭物及其制备方法，所述羟烷基淀粉共轭物包括羟烷基淀粉衍生物和细胞毒性药剂，所述细胞毒性药剂包括至少一个次级羟基，其中羟烷基淀粉通过所述次级羟基与细胞毒性药剂连接。根据本发明的共轭物具有以下公式HAS'(-L-M)n的结构，其中M是细胞毒性药剂的残基，L是连接基团，HAS'是羟烷基淀粉衍生物的残基，n大于或等于1，且羟烷基淀粉衍生物的平均分子量（MW）高于肾脏阈值。
• NOVEL WATER BASED PROCESS FOR THE PREPARATION OF SUBSTITUTED DIPHENYLMETHYL PIPERAZINES
  申请人：Lal Bansi

  公开号：US20110172425A1

  公开（公告）日：2011-07-14

  The present invention relates to a novel water based process for the preparation of substituted diphenylmethyl piperazines of Formula I and pharmaceutically acceptable salts wherein X 1 and X 2 represent independently a hydrogen, a halogen, a straight or branched chain lower alkyl, alkoxy or a hydroxyl radical and R is selected from groups such as acyl, alkyl, alkenyl, aralalkyl, aralalkenyl aralkyl, and aralalkenyl or aralkenyl hydroxyalkyl, aryloxyalkyl, alkoxyalkyl, aminoalkyl or its derivative comprising, reacting a compound of Formula II, with a compound of formula R—X where R is as defined above and X is suitable leaving group which includes halides, but not limiting use of other leaving groups such as tosylate, mesylate and activated acid groups such as acyl halide, anhydrides, mixed anhydrides etc. using water as a solvent, in presence of a catalyst and a base, at 25-100° C.;

  本发明涉及一种用水为基础的新型过程，用于制备化合物I的取代二苯甲基哌嗪及其药用盐，其中X1和X2分别代表氢、卤素、直链或支链低碳基、烷氧基或羟基基团，R选自酰基、烷基、烯基、芳基烷基、芳基烯基、芳基、芳基烯基或芳基羟基烷基、芳基氧基烷基、烷氧基烷基、氨基烷基或其衍生物等，包括将化合物II与化合物R-X反应，其中R如上定义，X是适当的离去基团，包括卤素等卤素，但不限于其他离去基团，如对甲苯磺酸酯、甲磺酸酯和活化酸基团，如酰卤、酸酐、混合酸酐等，使用水作为溶剂，在催化剂和碱的存在下，在25-100°C条件下进行。
• Renin inhibitors
  申请人：Jones Benjamin

  公开号：US20090105251A1

  公开（公告）日：2009-04-23

  Compounds, pharmaceutical compositions, kits and methods are provided for use with renin that comprise a compound selected from the group consisting of: wherein the variables are as defined herein.

  提供了与肾素一起使用的化合物、药物组合物、试剂盒和方法，其中包括从以下组中选择的化合物：其中变量如本文所定义。