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

4-Chloromethyl-N-(2-hydroxy-phenyl)-benzamide | 67563-28-4

中文名称
——
中文别名
——
英文名称
4-Chloromethyl-N-(2-hydroxy-phenyl)-benzamide
英文别名
4-(chloromethyl)-N-(2-hydroxyphenyl)benzamide
4-Chloromethyl-N-(2-hydroxy-phenyl)-benzamide化学式
CAS
67563-28-4
化学式
C14H12ClNO2
mdl
——
分子量
261.708
InChiKey
RGKDKSYDENLSLL-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):
    3.1
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    49.3
  • 氢给体数:
    2
  • 氢受体数:
    2

文献信息

  • Phenolic compound and recording material containing the same
    申请人:Hidaka Tomoya
    公开号:US20050096222A1
    公开(公告)日:2005-05-05
    An object of the present invention is to provide a novel phenolic compound, and a recording material containing the same, which is excellent in storage stability. The object can be achieved by a phenolic compound represented by the formula (I): [wherein m represents an integer of 0 to 2; R 1 and R 2 each independently represents a C1-C6 alkyl group or a C1-C6 alkoxy group; p and q each independently represents an integer of 0 to 4; t and u each independently represents 0 or 1 and do not simultaneously represent 0; and X represents a group represented by any of the formulas (II) to (VII): (wherein R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 11 each independently represents a hydrogen atom or a C1-C6 alkyl group; a represents an integer of 1 to 6; b represents an integer of 0 to 4; and c represents an integer of 0 to 6)] and a recording material containing the same.
    本发明的目的是提供一种新的酚类化合物和含有该化合物的记录材料,其具有良好的储存稳定性。所述目的可以通过由式(I)表示的酚类化合物实现:[其中,m表示0到2的整数;R1和R2各自独立地表示C1-C6烷基或C1-C6烷氧基;p和q各自独立地表示0到4的整数;t和u各自独立地表示0或1且不同时表示0;X表示由式(II)到(VII)中任意一种表示的基团:[其中,R3、R4、R5、R6、R7、R8、R9、R10和R11各自独立地表示氢原子或C1-C6烷基;a表示1到6的整数;b表示0到4的整数;c表示0到6的整数],以及含有该化合物的记录材料。
  • Phenolic Compound and Recording Material Using the Same
    申请人:NIPPON SODA CO., LTD.
    公开号:EP2161255A1
    公开(公告)日:2010-03-10
    A phenolic compound represented by the formula (XII): wherein R1, R2, R3, R4, R6, Y5, a, b, m, p, q, t and u are defined herein, is disclosed. A recording material containing a color developing dye comprising the phenolic compound is also disclosed.
    由式 (XII) 代表的酚类化合物: 其中 R1、R2、R3、R4、R6、Y5、a、b、m、p、q、t 和 u 在此定义。本发明还公开了一种含有由酚类化合物组成的显色染料的记录材料。
  • PROCESS FOR THE PREPARATION OF 4,4'-BIS(2-BENZOXAZOLYL)STILBENES
    申请人:Ciba Specialty Chemicals Holding Inc.
    公开号:EP1153018A1
    公开(公告)日:2001-11-14
  • US7169737B2
    申请人:——
    公开号:US7169737B2
    公开(公告)日:2007-01-30
  • [EN] PROCESS FOR THE PREPARATION OF 4,4'-BIS(2-BENZOXAZOLYL)STILBENES<br/>[FR] PROCEDE DE PREPARATION DE 4,4'-BIS(2-BENZOXAZOLYLE)STILBENES
    申请人:CIBA SC HOLDING AG
    公开号:WO2000044732A1
    公开(公告)日:2000-08-03
    A description is given of a simple and low cost process for the preparation and use of 4,4'-bis(2-benzoxazolyl)stilbene compounds of formula (1) (a) in a two-step process by reacting the compound of formula (2), with the aminophenol compound of formula (3) to give the compound of formula (5) and subsequently reacting the compound of formula (5) with a strong base to give the compound ofrmula (1); or (b) in a three-step process by reacting the compound of formula (2) with the amino compound of formula (3) to give the intermediate compound of formula (4), with subsequent ring-closure reaction of this compound to give the compound of formula (5) and subsequent reaction of the compound of formula (5) with a strong base to give the compound of formula (1); wherein in formulae (1), (3), (4) and (5) R1 is hydrogen; C1-C8alkyl; -CO2R2; -NHCOR2 or -OR2; and R2 is C1-C4alkyl. The stilbene compounds prepared according to this invention are used in polymeric materials, in particular in polyethylene terephthalate (PET).
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫