摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

propoxyacetic acid | 17640-31-2

中文名称
——
中文别名
——
英文名称
propoxyacetic acid
英文别名
n-propyl propoxyacetate;propoxy-acetic acid propyl ester;Propoxy-essigsaeure-propylester;Propylaetherglykolsaeurepropylester;Propyloxy-essigsaeure-propylester;Propyl 2-propoxyacetate
propoxyacetic acid化学式
CAS
17640-31-2
化学式
C8H16O3
mdl
——
分子量
160.213
InChiKey
BMVTVMIDGMNRRR-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

物化性质

  • 沸点:
    210.1±13.0 °C(Predicted)
  • 密度:
    0.940±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    11
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

点击查看最新优质反应信息

文献信息

  • 一种丙氧基乙酸的合成新工艺
    申请人:青岛和兴精细化学有限公司
    公开号:CN108299186B
    公开(公告)日:2021-02-12
    本发明公开了一种丙氧基乙酸的合成新工艺。该工艺包括下列步骤:1)反应:将丙醇钠分散于正丙醇中,向其中滴加氯乙酸的正丙醇溶液;滴加完毕,保温反应,用浓盐酸酸化;(2)除盐:过滤生成的氯化钠,滤饼用正丙醇淋洗,合并滤液与淋洗液;(3)精馏:滤液与淋洗液合并后,减压精馏,回收正丙醇,得到产品。本发明的有益效果:反应接近定量,产品总收率高达98%;废水不含盐,接近纯水,其各项指标均符合废水排放标准,可直接排放,不会造成环境污染,不会增加三废治理费用;滤出的盐用正丙醇洗涤回收有用成分后烘干,可作为副产出售。
  • Novel propionic acid derivatives
    申请人:——
    公开号:US20040072690A1
    公开(公告)日:2004-04-15
    A compound represented by the following formula (1) or a salt thereof: 1 wherein R 1 represents a C 1-12 alkyl group, phenyl group, 1-naphthyl group and the like, R 2 represents a C 2-12 alkyl group, (R 3 ) b represents 0 to 4 substituents such as a halogen atom, R 4 represents a lower alkyl group, R 5 represents hydrogen atom or a lower alkyl group, n represents an integer from 2 to 4, and X represents —NH— or —O—, which has superior hypoglycemic action, hypolipidemic action and total cholesterol reducing action, and is useful as an active ingredient of a medicament for prophylactic and/or therapeutic treatment of diseases including diabetes mellitus, hyperlipidemia and the like.
    以下化合物的分子式(1)或其盐:其中R1代表C1-12烷基基团、苯基、1-萘基等,R2代表C2-12烷基基团,(R3)b代表0至4个卤原子等取代基,R4代表较低的烷基基团,R5代表氢原子或较低的烷基基团,n代表2至4的整数,X代表—NH—或—O—,具有优越的降糖作用、降脂作用和总胆固醇降低作用,可用作预防和/或治疗糖尿病、高脂血症等疾病的药物的活性成分。
  • [EN] PROCESS FOR PRODUCING OPTICALLY ACTIVE 3-(4-HYDROXYPHENYL)PROPIONIC ACIDS<br/>[FR] PROCEDE DE PRODUCTION D'ACIDES 3-(4-HYDROXYPHENYL)PROPIONIQUES OPTIQUEMENT ACTIFS
    申请人:TAKASAGO PERFUMERY CO LTD
    公开号:WO2005051882A1
    公开(公告)日:2005-06-09
    The present invention relates to a process for producing an optically active 3-(4-hydroxyphenyl)propionic acid useful as intermediates for medicines, through short steps in good yield and with high optical purity. More specifically, the present invention relates to a process for producing an optically active 3-(4-hydroxyphenyl)propionic acid of the formula (6): wherein R2 is an alkyl group; R5 to R8 are each independently a hydrogen atom or a substituent; and the symbol * is an chiral carbon atom, or a salt thereof, which comprises reacting a benzaldehyde of the formula (1): wherein R1 is a protective group; and R5 to R8 are each the same as defined above, with a glycolic acid derivative of the formula (2): wherein R3 is a hydrocarbon group; and R2 is the same as defined above, hydrolyzing the resulting product to give a cinnamic acid of the formula (4): wherein R1, R2 and R5 to R8 are each the same as defined above, or a salt thereof, and subjecting the resulting cinnamic acid (4) or a salt thereof to asymmetric hydrogenation to give an optically active phenylpropionic acid of the formula (5): wherein all the symbols are each the same as defined above, or a salt thereof, followed by deprotection.
    本发明涉及一种生产光学活性3-(4-羟基苯基)丙酸的工艺,作为药物中间体,通过简短的步骤、高产率和高光学纯度。更具体地,本发明涉及一种生产光学活性3-(4-羟基苯基)丙酸的工艺,其化学结构如下(6):其中R2是烷基;R5至R8分别独立地是氢原子或取代基;符号*是一个手性碳原子,或其盐,包括将化学结构如下(1)的苯甲醛:其中R1是保护基;R5至R8分别与上述定义相同,与化学结构如下(2)的甘醇酸衍生物反应:其中R3是烃基;R2与上述定义相同,水解得到肉桂酸的产物:其中R1、R2和R5至R8分别与上述定义相同,或其盐,并将得到的肉桂酸(4)或其盐进行不对称氢化反应,得到光学活性苯丙酸的产物:其中所有符号均与上述定义相同,或其盐,随后进行去保护处理。
  • Process for producing optically active 3-(4-hydroxyphenyl)proprionic acids
    申请人:Yokozawa Tohru
    公开号:US20070142472A1
    公开(公告)日:2007-06-21
    The present invention relates to a process for producing an optically active 3-(4-hydroxyphenyl)propionic acid useful as intermediates for medicines, through short steps in good yield and with high optical purity. More specifically, the present invention relates to a process for producing an optically active 3-(4-hydroxyphenyl)propionic acid of the formula (6): wherein R 2 is an alkyl group; R 5 to R 8 are each independently a hydrogen atom or a substituent; and the symbol * is an chiral carbon atom, or a salt thereof, which comprises reacting a benzaldehyde of the formula (1): wherein R 1 is a protective group; and R 5 to R 8 are each the same as defined above, with a glycolic acid derivative of the formula (2): wherein R 3 is a hydrocarbon group; and R 2 is the same as defined above, hydrolyzing the resulting product to give a cinnamic acid of the formula (4): wherein R 1 , R 2 and R 5 to R 8 are each the same as defined above, or a salt thereof, and subjecting the resulting cinnamic acid (4) or a salt thereof to asymmetric hydrogenation to give an optically active phenylpropionic acid of the formula (5): wherein all the symbols are each the same as defined above, or a salt thereof, followed by deprotection.
    本发明涉及一种生产光学活性的3-(4-羟基苯基)丙酸的方法,该方法通过短步骤以良好产率和高光学纯度的方式,作为药物中间体。更具体地说,本发明涉及一种生产式(6)的光学活性3-(4-羟基苯基)丙酸的方法:其中R2是烷基;R5到R8分别独立地是氢原子或取代基;符号*是手性碳原子,或其盐,包括用式(1)的苯甲醛反应:其中R1是保护基;R5到R8分别与上述定义相同,与式(2)的乙二醇酸衍生物反应:其中R3是碳氢基团;R2与上述定义相同,水解所得产物得到式(4)的肉桂酸:其中R1、R2和R5到R8分别与上述定义相同,或其盐,并将所得的肉桂酸(4)或其盐经过不对称氢化作用得到式(5)的光学活性苯丙酸:其中所有符号均与上述定义相同,或其盐,然后去保护基。
  • METHOD FOR PRODUCING EPOXY COMPOUND HAVING CYANURIC ACID SKELETON
    申请人:Takeyama Toshiaki
    公开号:US20130172525A1
    公开(公告)日:2013-07-04
    There is provided an epoxy compound that provides properties of cured products combining high transparency with high flexural strength by being thermally cured while maintaining advantageous handling properties in a liquid state thereof; and a method for producing a composition by using the epoxy compound. A method for producing an epoxy compound of Formula (1): (in Formula (1), n1, n2, and n3 are individually any one of integers of 2 to 6; n4, n5, and n6 are individually an integer of 2; n7, n8, and n9 are individually an integer of 1; and R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 are independently a hydrogen atom or a C 1-10 alkyl group), including: reacting cyanuric chloride with a C 4-8 alkenol and reacting the obtained compound having an unsaturated bond with a peroxide.
    本发明提供了一种环氧化合物,通过在液态下保持有利的处理性能,热固化后具有高透明度和高弯曲强度的固化产品特性;以及使用该环氧化合物制备组合物的方法。一种制备式(1)环氧化合物的方法:(在式(1)中,n1、n2和n3分别为2至6的任意整数;n4、n5和n6分别为2的整数;n7、n8和n9分别为1的整数;R1、R2、R3、R4、R5和R6独立地为氢原子或C1-10烷基)包括:将三聚氰氯与C4-8烯醇反应,并将所得具有不饱和键的化合物与过氧化物反应。
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物