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α-nitrooxymethyl-2,4-dinitrobenzenepropanoic acid methyl ester | 1042973-02-3

中文名称
——
中文别名
——
英文名称
α-nitrooxymethyl-2,4-dinitrobenzenepropanoic acid methyl ester
英文别名
Methyl 2-[(2,4-dinitrophenyl)methyl]-3-nitrooxypropanoate;methyl 2-[(2,4-dinitrophenyl)methyl]-3-nitrooxypropanoate
α-nitrooxymethyl-2,4-dinitrobenzenepropanoic acid methyl ester化学式
CAS
1042973-02-3
化学式
C11H11N3O9
mdl
——
分子量
329.223
InChiKey
YPUPYLHUKJDESS-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):
    2
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    173
  • 氢给体数:
    0
  • 氢受体数:
    9

反应信息

点击查看最新优质反应信息

文献信息

  • HETEROCYCLIDENE-N-(ARYL) ACETAMIDE DERIVATIVE
    申请人:UCHIDA Hideharu
    公开号:US20100016285A1
    公开(公告)日:2010-01-21
    The blow-described formula (I) [Ch. 1] a compound represented by formula (I) (wherein k, m, n, and p each represent 0 to 2; j and q represents 0 or 1; R 1 represents a halogen atom, a hydrocarbon group, a heterocyclic group, an alkoxy group, an alkoxycarbonyl group, NH 2 , OH, a carboxyl group, an alkanoyl group, CN, NO 2 , or the like; R 2 represents a halogen atom, an amino group, a hydrocarbon group, an aromatic heterocyclic group, an oxo group, or the like; represents an oxygen atom, —NR 3 —, or —S(O)r- (wherein r is an integer of 0 to 2); X 2 represents a methylene group, an oxygen atom, —NR 3 — (wherein R 3 is a hydrogen atom, a hydrocarbon group, or the like), or S(O)r- (wherein r is an integer of 0 to 2); W represents a methylene group, a carbonyl group, or a sulfonyl group; R 7 represents a hydrogen atom, a hydrocarbon group, a heterocyclic group, or the like; R 8 represents a hydrogen atom, a halogen atom, a hydrocarbon group, a heterocyclic group, the broken line in the ring containing X 1 and X 2 represents a condensation of two rings; cycle moiety represents a five- or six-membered aryl ring or heteroaryl ring; and the solid line and the broken line between L 1 and L 2 are a single bond or double bond, and the wavy line represents an E-isomer or a Z-isomer), a salt thereof, or solvates thereof, and a pharmaceutical composition containing the compound as an active ingredient.
    以下是所描述的公式(I)[Ch. 1]的化合物,由公式(I)表示(其中k、m、n和p各自表示0到2;j和q表示0或1;R1表示卤素原子、碳氢基团、杂环基团、烷氧基、烷氧羰基基团、NH2、OH、羧基、烷酰基、CN、NO2或类似物;R2表示卤素原子、氨基基团、碳氢基团、芳香杂环基团、氧代基团或类似物;表示氧原子、-NR3-或-S(O)r-(其中r为0至2的整数);X2表示亚甲基基团、氧原子、-NR3-(其中R3为氢原子、碳氢基团或类似物)或S(O)r-(其中r为0至2的整数);W表示亚甲基基团、羰基基团或磺酰基基团;R7表示氢原子、碳氢基团、杂环基团或类似物;R8表示氢原子、卤素原子、碳氢基团、杂环基团,环中的X1和X2之间的断线表示两个环的缩合;环基表示五元或六元芳基环或杂芳基环;实线和L1和L2之间的断线是单键或双键,波浪线表示E-异构体或Z-异构体),其盐或溶剂化物,以及含有该化合物作为活性成分的药物组成物。
  • HETEROCYCLIDENE-N-(ARYL)ACETAMIDE DERIVATIVE
    申请人:MOCHIDA PHARMACEUTICAL CO., LTD.
    公开号:EP2128157A1
    公开(公告)日:2009-12-02
    The blow-described formula (I): [Ch. 1] a compound represented by formula (I) : (wherein k, m, n, and p each represent 0 to 2; j and q represents 0 or 1; R1 represents a halogen atom, a hydrocarbon group, a heterocyclic group, an alkoxy group, an alkoxycarbonyl group, NH2, OH, a carboxyl group, an alkanoyl group, CN, NO2, or the like; R2 represents a halogen atom, an amino group, a hydrocarbon group, an aromatic heterocyclic group, an oxo group, or the like; X1 represents an oxygen atom, -NR3-, or -S(O)r- (wherein r is an integer of 0 to 2); X2 represents a methylene group, an oxygen atom, -NR3- (wherein R3 is a hydrogen atom, a hydrocarbon group, or the like), or -S(O)r- (wherein r is an integer of 0 to 2); W represents a methylene group, a carbonyl group, or a sulfonyl group; R7 represents a hydrogen atom, a hydrocarbon group, a heterocyclic group, or the like; R8 represents a hydrogen atom, a halogen atom, a hydrocarbon group, a heterocyclic group, the broken line in the ring containing X1 and X2 represents a condensation of two rings; cycle moiety represents a five- or six-memebered aryl ring or heteroaryl ring; and the solid line and the broken line between L1 and L2 are a single bond or double bond, and the wavy line represents an E-isomer or a Z-isomer), a salt thereof, or solvates thereof, and a pharmaceutical composition containing the compound as an active ingredient.
    吹气式(I): [1] 式 (I) 所代表的化合物: (其中 k、m、n 和 p 分别代表 0 至 2;j 和 q 代表 0 或 1;R1 代表卤素原子、烃基、杂环基、烷氧基、烷氧羰基、NH2、OH、羧基、烷酰基、CN、NO2 或类似物;X1 代表氧原子、-NR3- 或 -S(O)r- (其中 r 为 0 至 2 的整数); X2 代表亚甲基、氧原子、-NR3- (其中 R3 为氢原子、烃基或类似基团)或 -S(O)r- (其中 r 为 0 至 2 的整数);W 代表亚甲基、羰基或磺酰基; R7 代表氢原子、烃基、杂环基或类似基团; R8 代表氢原子、卤素原子、烃基、杂环基;L1和L2之间的实线和断线为单键或双键,波浪线代表E-异构体或Z-异构体)、其盐或其溶物,以及含有该化合物作为活性成分的药物组合物。
  • NEW HYDROXYPHENYL DERIVATIVES AND BIOLOGICAL APPLICATIONS THEREOF
    申请人:Mutabilis SA
    公开号:EP2010495A2
    公开(公告)日:2009-01-07
  • [EN] NEW HYDROXYPHENYL DERIVATIVES AND BIOLOGICAL APPLICATIONS THEREOF<br/>[FR] NOUVEAUX DÉRIVÉS D'HYDROXYPHÉNYLE ET LEURS APPLICATIONS BIOLOGIQUES
    申请人:MUTABILIS S A
    公开号:WO2007135562A2
    公开(公告)日:2007-11-29
    [EN] The invention relates to hydroxyphenyl derivatives of formula (I) wherein R1 is phenyl or a 6 membered monocyclic nitrogenous heteroaryl of formula wherein Z4, Z5, Z6, Z7 and Z8 are C or N with a maximum of three N, R1 being possibly substituted by 1 to 3 R identical or different, - R2 is phenyl, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, C1- C4f luoro-alkyl, C2-C4f luoro-alkenyl, OR3, SRa, all being possibly substituted by 1 to 3 identical or different R', - Ra,Rb and Rc, are H, C1-C8 alkyl, C2-C8 alkenyl, C2-C8 alkynyl, phenyl, heteroaryl and aliphatic heterocycle as defined above for R2, the heteroaryl and the heterocycle being possibly formed with the carbon and nitrogen atoms to which Ra, Rb and Rc are linked, - R' is heteroaryl and aliphatic heterocycle as defined above for R2, C1-C8 alkyl, CH2CO2R", CO2R", COR", CONR"R"', OCOR", OR", NR"R"', NR"C0R'", NR"COOR"', OCONR"R"', NR"CONR"R"', NR"SO2R"', SO2R", NR"SO2R"', halogen and CN, R" and R"', identical or different, are H, C1-C8 alkyl or form together a 4 to 6 membered heterocycle with 1 to 3 heteroatoms selected from N, 0 and S, - Y represents H or a labile chemical group able to regenerate in vivo the free phenol - Z1 and Z3 are halogen or H, and Z2 is fluor or H, provided that - either Z2 is fluor and all the other definitions are as defined above, - or Z6 is a carbon atom substituted by R as defined above, R being different from H, alkyl, halogen, NH2, OH, CONH2 or fluoro alkyl and all the other definitions are as defined above, - or Z4 or Z5, or Z7 or Z8 are carbon atoms substituted by NRaRb or ORa, ORa being different from OH and all the other definitions are as defined above, - or Z5, or Z7, is a carbon atom substituted by R, R being different from H and all the other definitions are as defined above, - or R2 is a C1-C8alkyl-heteroaryl radical or a C1- C8alkyl-ORa radical, 0Ra being different from OH and all the other definitions are as defined above. Applications as anti-bacterial and/or anti-parasites agents.
    [FR] L'invention concerne des dérivés d'hydroxyphényle de formule (I), dans laquelle R1 est un phényle ou un hétéroaryle azoté monocyclique à 6 éléments de formule où Z4, Z5, Z6, Z7 et Z8 représentent C ou N avec un maximum de trois N, R1 étant éventuellement substitué par 1 à 3 R identiques ou différents, - R2 est un phényle, C1-C8 alkyle, C2-C8 alcényle, C2-C8 alkynyle, C1- C4f luoro-alkyle, C2-C4fluoro-alcényle, ORa, SRa, tous étant éventuellement substitués par 1 à 3 R' identiques ou différents, - Ra,Rb et Rc, représentent H, C1-C8 alkyle, C2-C8 alcényle, C2-C8 alkynyle, un phényle, un hétéroaryle et un hétérocycle aliphatique comme susmentionné pour R2, l'hétéroaryle et l'hétérocycle étant éventuellement formés avec les atomes de carbone et d'azote auxquels Ra, Rb et Rc sont liés, - R' est un hétéroaryle et un hétérocycle aliphatique comme susmentionné pour R2, C1-C8 alkyle, CH2CO2R", CO2R", COR", CONR"R"', OCOR", OR", NR"R"', NR"C0R'", NR"COOR"', OCONR"R"', NR"CONR"R"', NR"SO2R"', SO2R", NR"SO2R"', halogène et CN, R" et R"', identiques ou différents, représentent H, C1-C8 alkyle ou forment ensemble un hétérocycle de 4 à 6 éléments avec 1 à 3 hétéroatomes choisis parmi N, 0 et S, - Y représente H ou un groupe chimique labile capable de régénérer in vivo le phénol libre, - Z1 et Z3 représentent halogène ou H, et Z2 est un fluor ou H, à condition que Z2 soit un fluor et toutes les autres définitions soient telles que susmentionnées, ou que Z6 soit un atome de carbone substitué par R comme précité, R étant différent de H, alkyle, halogène, NH2, OH, CONH2 ou fluoro alkyle et que toutes les autres définitions soient telles que susmentionnées, ou que Z4, Z5, Z7 ou Z8 soient des atomes de carbone substitués par NRaRb ou ORa, ORa étant différent de OH et que toutes les autres définitions soit telles que précitées, ou que Z5 ou Z7 soit un atome de carbone substitué par R, R étant différent de H et que toutes les autres définitions soient identiques à celles susmentionnées, ou que R2 représente un radical C1-C8alkyl-hétéroaryle ou un radical C1- C8alkyl-ORa, 0Ra étant différent de OH et que toutes les définitions soient semblables à celles précitées. Cette invention a aussi pour objet des applications de ces dérivés en tant qu'agents antibactériens et/ou antiparasites.
  • EP2128157
    申请人:——
    公开号:——
    公开(公告)日:——
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