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

1-(4-叔丁基苯基)-2-癸基-3-(4-甲氧基苯基)丙烷-1,3-二酮 | 828911-21-3

中文名称
1-(4-叔丁基苯基)-2-癸基-3-(4-甲氧基苯基)丙烷-1,3-二酮
中文别名
——
英文名称
1-(4-tert-butylphenyl)-2-decanyl-3-(4-methoxyphenyl)propane-1,3-dione
英文别名
C10-DBM;3-(4-tert-butylphenyl)-2-decanyl-1-(4-methoxyphenyl)propane-1,3-dione;1-(4-t-Butylphenyl)-2-decanyl-3-(4'-methoxyphenyl)-propane 1,3-dione;1-(4-tert-butylphenyl)-2-decyl-3-(4-methoxyphenyl)propane-1,3-dione
1-(4-叔丁基苯基)-2-癸基-3-(4-甲氧基苯基)丙烷-1,3-二酮化学式
CAS
828911-21-3
化学式
C30H42O3
mdl
——
分子量
450.662
InChiKey
OYGPDIGLEKMQFB-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:
    572.4±40.0 °C(Predicted)
  • 密度:
    0.994±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    10
  • 重原子数:
    33
  • 可旋转键数:
    15
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:afa986cdda64f6a0d37ce61792025f97
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Photochemical Behavior of a New Long-chain UV Absorber† Derived from 4-tert-Butyl-4′-Methoxydibenzoylmethane¶
    摘要:
    A new UV filter, the 1-(4-tert-butylphenyl)-2-decanyl-3-(4'-methoxyphenyl)-propane-1,3-dione, called C10-DBM, was prepared by grafting a 10-carbon aliphatic chain to the alpha-carbonyl position of 4-tert-butyl-4'-methoxydibenzoylmethane (BM-DBM), a well-known and often used UV filter. The UV-A absorption efficiency of organic solutions containing the new filter was tested and compared with identical solutions containing BM-DBM with or without irradiation (xenon lamp). The originality of this new filter is that its UV-A absorbance appeared during irradiation of the molecule. Although the molar absorption coefficient of C10-DBM in the UV-A domain was lower than that of BM-DBM, the solutions absorption exhibited a much more photostable behavior under irradiation. In this study, we first demonstrated that C10-DBM was a precursor of BM-DBM (enol isomer) by means of high-performance liquid chromatography followed by mass spectrometry. Indeed, we showed that the UV-A absorption of C10-DBM solutions appearing during the irradiation of the molecule was due to a Norrish-II reaction (beta-cleavage), which induced the release of the BM-DBM enol form and 1-decene. Then, we established a kinetic model for the photochemistry of C10-DBM and fitted the variation of UV absorption spectra to confirm the proposed mechanism.
    DOI:
    10.1562/2004-03-09-ra-106.1
  • 作为产物:
    描述:
    癸基溴阿伏苯宗四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以42%的产率得到1-(4-叔丁基苯基)-2-癸基-3-(4-甲氧基苯基)丙烷-1,3-二酮
    参考文献:
    名称:
    Photochemical Behavior of a New Long-chain UV Absorber† Derived from 4-tert-Butyl-4′-Methoxydibenzoylmethane¶
    摘要:
    A new UV filter, the 1-(4-tert-butylphenyl)-2-decanyl-3-(4'-methoxyphenyl)-propane-1,3-dione, called C10-DBM, was prepared by grafting a 10-carbon aliphatic chain to the alpha-carbonyl position of 4-tert-butyl-4'-methoxydibenzoylmethane (BM-DBM), a well-known and often used UV filter. The UV-A absorption efficiency of organic solutions containing the new filter was tested and compared with identical solutions containing BM-DBM with or without irradiation (xenon lamp). The originality of this new filter is that its UV-A absorbance appeared during irradiation of the molecule. Although the molar absorption coefficient of C10-DBM in the UV-A domain was lower than that of BM-DBM, the solutions absorption exhibited a much more photostable behavior under irradiation. In this study, we first demonstrated that C10-DBM was a precursor of BM-DBM (enol isomer) by means of high-performance liquid chromatography followed by mass spectrometry. Indeed, we showed that the UV-A absorption of C10-DBM solutions appearing during the irradiation of the molecule was due to a Norrish-II reaction (beta-cleavage), which induced the release of the BM-DBM enol form and 1-decene. Then, we established a kinetic model for the photochemistry of C10-DBM and fitted the variation of UV absorption spectra to confirm the proposed mechanism.
    DOI:
    10.1562/2004-03-09-ra-106.1
点击查看最新优质反应信息

文献信息

  • Dibenzoilmethane derivative compounds, the use thereof in the form of photoactivable solar filters and cosmetic compositions containing said compounds
    申请人:Rico-Lattes Isabelle
    公开号:US20070025930A1
    公开(公告)日:2007-02-01
    The present invention relates to dibenzoylmethane-based compounds of formula 1, and also to salts or solvates thereof, and to the process for preparing them. The invention also relates to the use of a compound of formula (I) as an agent for protecting the skin or the hair against UV radiation and to a cosmetic and/or dermatological product, characterized in that it comprises a compound of formula (I) as active principle.
    本发明涉及公式1的二苯甲酮基化合物,以及其盐或溶剂化物,以及其制备过程。本发明还涉及将公式(I)化合物用作保护皮肤或头发免受紫外线辐射的剂量,以及化妆品和/或皮肤科产品,其特征在于其包含公式(I)化合物作为活性成分。
  • US7446230B2
    申请人:——
    公开号:US7446230B2
    公开(公告)日:2008-11-04
查看更多

同类化合物

(2Z)-1,3-二苯基-2-丙烯-1-酮,2-丙烯-1-酮,1,3-二苯基-,(2Z)- 龙血素D 龙血素A 龙血素 B 黄色当归醇F 黄色当归醇B 黄腐醇; 黄腐酚 黄腐醇 D; 黄腐酚 D 黄腐酚B 黄腐酚 黄腐酚 黄卡瓦胡椒素 C 高紫柳查尔酮 阿普非农 阿司巴汀 阿伏苯宗 金鸡菊查耳酮 邻肉桂酰苯甲酸 达泊西汀杂质25 豆蔻明 补骨脂色烯查耳酮 补骨脂查耳酮 补骨脂呋喃查耳酮 补骨脂乙素 蜡菊亭; 4,2',4'-三羟基-6'-甲氧基查耳酮 苯酚,4-[3-(2-羟基苯基)-1-苯基丙基]-2-(3-苯基丙基)- 苯磺酰胺,N-[4-[3-(3-羟基苯基)-1-羰基-2-丙烯基]苯基]- 苯磺酰胺,N-[3-[3-(4-羟基-3-甲氧苯基)-1-羰基-2-丙烯基]苯基]- 苯磺酰胺,4-甲氧基-N,N-二甲基-2-(3-羰基-3-苯基-1-丙烯基)-,(E)- 苯磺酰氯化,4,5-二甲氧基-2-(3-羰基-3-苯基-1-丙烯基)-,(E)- 苯磺酰氯,4-甲氧基-3-(3-羰基-3-苯基-1-丙烯基)-,(E)- 苯甲醇,4-甲氧基-a-[2-(4-甲氧苯基)乙烯基]- 苯甲酸-[4-(3-氧代-3-苯基-丙烯基)-苯胺] 苯甲酸,3-[3-(4-溴苯基)-1-羰基-2-丙烯基]-4-羟基- 苯甲酰(2-羟基苯酰)甲烷 苯甲腈,4-(1-羟基-3-羰基-3-苯基丙基)- 苯基[2-(1-萘基)乙烯基]甲酮 苯基-(三苯基-丙-2-炔基)-醚 苯基-(2-苯基-2,3-二氢-苯并噻唑-2-基)-甲酮 苯亚甲基苯乙酮 苯乙酰腈,a-(1-氨基-2-苯基亚乙基)- 苯丙酸,a-苯甲酰-b-羰基-,苯基(苯基亚甲基)酰肼 苯,1-(2,2-二甲基-3-苯基丙基)-2-甲基- 苏木查耳酮 苄桂哌酯 苄基(4-氯-2-(3-氧代-1,3-二苯基丙基)苯基)氨基甲酸酯 芦荟提取物 腈苯唑 胀果甘草宁C 聚磷酸根皮酚