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3-(diethylaminomethyl-phenyl)-1-(4-methoxy-phenyl)-4-nitro-butan-1-one | 862201-31-8

中文名称
——
中文别名
——
英文名称
3-(diethylaminomethyl-phenyl)-1-(4-methoxy-phenyl)-4-nitro-butan-1-one
英文别名
3-(4-diethylaminomethylphenyl)-1-(4-methoxyphenyl)-4-nitrobutan-1-one;3-(4-diethylaminomethylphenyl)-l-(4-methoxyphenyl)-4-nitrobutan-1-one;3-[4-(Diethylaminomethyl)phenyl]-1-(4-methoxyphenyl)-4-nitrobutan-1-one
3-(diethylaminomethyl-phenyl)-1-(4-methoxy-phenyl)-4-nitro-butan-1-one化学式
CAS
862201-31-8
化学式
C22H28N2O4
mdl
——
分子量
384.475
InChiKey
HTHRBJNSPPOHIL-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:
    543.6±50.0 °C(Predicted)
  • 密度:
    1.124±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    28
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    75.4
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    参考文献:
    名称:
    A Modular Synthesis of Unsymmetrical Tetraarylazadipyrromethenes
    摘要:
    A stepwise route to unsymmetrical tetraarylazadipyrromethenes by a condensation of 2,4-diaryl-5-nitroso-pyrroles with 2,4-diarylpyrroles is described. This modular building-block approach allows for the introduction of up to four different aryl substituents on the azadipyrromethene and is tolerant of a varied substituent set. An efficient synthesis of the 2,4-diarylpyrroles building blocks from 1,3-diaryl-4-nitro-butan-1-ones by nitro hydrolysis to a keto-aldehyde and subsequent ammonia condensation reaction has been achieved. The facile conversion of 2,4-diarylpyrroles into their alpha-nitroso analogues by their reaction with sodium nitrite generated the second building block required for the synthesis.
    DOI:
    10.1021/jo050696k
  • 作为产物:
    参考文献:
    名称:
    A Modular Synthesis of Unsymmetrical Tetraarylazadipyrromethenes
    摘要:
    A stepwise route to unsymmetrical tetraarylazadipyrromethenes by a condensation of 2,4-diaryl-5-nitroso-pyrroles with 2,4-diarylpyrroles is described. This modular building-block approach allows for the introduction of up to four different aryl substituents on the azadipyrromethene and is tolerant of a varied substituent set. An efficient synthesis of the 2,4-diarylpyrroles building blocks from 1,3-diaryl-4-nitro-butan-1-ones by nitro hydrolysis to a keto-aldehyde and subsequent ammonia condensation reaction has been achieved. The facile conversion of 2,4-diarylpyrroles into their alpha-nitroso analogues by their reaction with sodium nitrite generated the second building block required for the synthesis.
    DOI:
    10.1021/jo050696k
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文献信息

  • [EN] FLUORESCENT NEAR INFRA-RED (NIR) DYES<br/>[FR] COLORANTS FLUORESCENTS DANS LE PROCHE INFRAROUGE (NIR)
    申请人:HAE THERAPEUTICS
    公开号:WO2011048217A1
    公开(公告)日:2011-04-28
    A compound of formula (I) is described in which each A, which may be the same or different, is a halide selected from fluoride, chloride, bromide and iodide, or is O-Y, wherein Y is a substituted or unsubstituted, saturated or unsaturated, straight or branched chain alkyl moiety. R1, R2, R3, R6, R7, and R8 are each independently H, OH, NO2 or O-L-X, wherein L is a spacer group, and X is a conjugation group or a water- solubilizing group. At least one of R1, R2, R3 is OH or O-L-X and at least one of R6, R7, and R8 is OH or O-L-X. R4 and R5, which may be the same or different, are each independently H; or are a substituted or unsubstituted, saturated or unsaturated, cyclic moiety; a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; or a substituted or unsubstituted, saturated or unsaturated, straight or branched chain alkyl moiety. Also described are dye conjugates comprising a compound of the invention.
    化合物的结构式(I)中描述了每个A,它可以相同也可以不同,是从化物、化物、化物和化物中选择的卤素,或者是O-Y,其中Y是取代或未取代的、饱和或不饱和的、直链或支链烷基基团。R1、R2、R3、R6、R7和R8各自独立地是H、OH、NO2或O-L-X,其中L是一个间隔基团,X是一个共轭基团或溶性基团。R1、R2、R3中至少有一个是OH或O-L-X,R6、R7和R8中至少有一个是OH或O-L-X。R4和R5,它们可以相同也可以不同,各自独立地是H;或者是一个取代或未取代的、饱和或不饱和的、环状基团;一个取代或未取代的、饱和或不饱和的杂环基团;或者是一个取代或未取代的、饱和或不饱和的、直链或支链烷基基团。还描述了包含本发明化合物的染料结合物。
  • FLUORESCENT NEAR INFRA-RED (NIR) DYES
    申请人:O'Shea Donal
    公开号:US20120232282A1
    公开(公告)日:2012-09-13
    A compound of formula (I) is described in which each A, which may be the same or different, is a halide selected from fluoride, chloride, bromide and iodide, or is O—Y, wherein Y is a substituted or unsubstituted, saturated or unsaturated, straight or branched chain alkyl moiety. R 1 , R 2 , R 3 , R 6 , R 7 , and R 8 are each independently H, OH, NO 2 or O-L-X, wherein L is a spacer group, and X is a conjugation group or a water-solubilizing group. At least one of R 1 , R 2 , R 3 is OH or O-L-X and at least one of R 6 , R 7 , and R 8 is OH or O-L-X. R 4 and R 5 , which may be the same or different, are each independently H; or are a substituted or unsubstituted, saturated or unsaturated, cyclic moiety; a substituted or unsubstituted, saturated or unsaturated heterocyclic moiety; or a substituted or unsubstituted, saturated or unsaturated, straight or branched chain alkyl moiety. Also described are dye conjugates comprising a compound of the invention.
    公式(I)描述了一种化合物,其中每个A(可以相同也可以不同)是从化物、化物、化物和化物中选择的卤素,或者是O—Y,其中Y是取代或未取代的、饱和或不饱和的、直链或支链烷基基团。R1、R2、R3、R6、R7和R8分别独立地是H、OH、NO2或O-L-X,其中L是一个间隔基团,X是一个共轭基团或溶性基团。R1、R2、R3中至少一个是OH或O-L-X,R6、R7和R8中至少一个是OH或O-L-X。R4和R5(可以相同也可以不同)分别独立地是H;或者是取代或未取代的、饱和或不饱和的、环状基团;取代或未取代的、饱和或不饱和的杂环基团;或者取代或未取代的、饱和或不饱和的、直链或支链烷基基团。还描述了包括本发明化合物的染料共轭物。
  • Water-solubilised BF<sub>2</sub>-chelated tetraarylazadipyrromethenes
    作者:Mariusz Tasior、Julie Murtagh、Daniel O. Frimannsson、Shane O. McDonnell、Donal F. O'Shea
    DOI:10.1039/b919546g
    日期:——
    Strategic incorporation of sulfonic acid, carboxylic acid or ammonium salt motifs generate water soluble BF2-chelated tetraarylazadipyrromethenes which exhibit strong near infra-red (NIR) emissions above 720 nm and can be readily imaged in both eukaryotic and prokaryotic cells.
    战略性地整合磺酸羧酸盐基团,生成溶性BF2-螯合的四芳基亚吡咯烷,这些化合物在720 nm以上展现出强烈的近红外(NIR)发射,并且可以在真核细胞和原核细胞中轻松成像。
  • US8907107B2
    申请人:——
    公开号:US8907107B2
    公开(公告)日:2014-12-09
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