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2',4'-Dihydroxyacetophenone oxime | 850925-13-2

中文名称
——
中文别名
——
英文名称
2',4'-Dihydroxyacetophenone oxime
英文别名
Resacetophenon-oxim;1-(2,4-dihydroxyphenyl)ethanone oxime;(1E)-1-(2,4-Dihydroxyphenyl)ethanone oxime;4-[(E)-N-hydroxy-C-methylcarbonimidoyl]benzene-1,3-diol
2',4'-Dihydroxyacetophenone oxime化学式
CAS
850925-13-2
化学式
C8H9NO3
mdl
——
分子量
167.164
InChiKey
FQPRUMXSHZSJGM-WEVVVXLNSA-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):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    73
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    2',4'-Dihydroxyacetophenone oxime异丁酰胺三氯氧磷 作用下, 以 乙腈 为溶剂, 反应 0.5h, 以83%的产率得到6-羟基-2-甲基苯并恶唑
    参考文献:
    名称:
    The Beckmann Rearrangement by Means of Phosphoryl Chloride/N,N-Dimethylacetamide; A Novel and Convenient Method for Preparing Benzoxazoles
    摘要:
    DOI:
    10.1055/s-1982-29704
  • 作为产物:
    参考文献:
    名称:
    EL-KASABY, M. A.;SALEM, M. A. I., EGYPT. J. CHEM., 1980, 23, N 2, 123-136
    摘要:
    DOI:
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文献信息

  • 5-Thioxylopyranose Compounds
    申请人:THOMAS Didier
    公开号:US20090118325A1
    公开(公告)日:2009-05-07
    5-thioxylose compounds, especially 5-thioxylopyranose compounds, a process for their preparation, and their use for treating and/or inhibiting thromboses, especially venous thromboses. The compounds correspond to formula I: in which the pentapyranosyl group represents a free or substituted 5-thio-β-D-xylopyranosyl group; R′, R″ and R′″ each independently represent a hydrogen atom, a C 2 -C 6 acyl group, or two adjacent ones of them form a 1-methylethylidene bridge; X 1 and X 2 each represent carbon or nitrogen; Y 1 and Y 2 each independently represent carbon, nitrogen, sulfur or oxygen, with the proviso that if Y 2 represents oxygen or sulfur, then Y 1 represents carbon or nitrogen; R 1 , R 2 , R 3 , R 4 and R 5 each independently represent hydrogen, a COOR 6 group where R 6 represents hydrogen or a C 1 -C 4 alkyl group optionally substituted by a phenyl ring, a halogen atom or a —COOR 6 group; a C 1 -C 4 alkoxy group; a C 1 -C 6 acyl group; a benzoyl group or a phenyl ring; and the addition salts and/or active metabolites of such compounds.
    含有5-硫氧基木糖化合物,尤其是5-硫氧基吡喃糖化合物,其制备方法,以及它们用于治疗和/或抑制血栓症,尤其是静脉血栓症。这些化合物对应于式I:其中五元吡喃糖基代表自由或取代的5-硫基-β-D-木糖吡喃糖基;R'、R"和R'"各自独立地代表氢原子、C2-C6酰基团,或其中的两个相邻的形成1-甲基乙烯基桥;X1和X2各代表碳或氮;Y1和Y2各自独立地代表碳、氮、硫或氧,但如果Y2代表氧或硫,则Y1代表碳或氮;R1、R2、R3、R4和R5各自独立地代表氢、COOR6基团,其中R6代表氢或C1-C4烷基基团,该基团可选地被苯环、卤素原子或-COOR6基团取代;C1-C4烷氧基团;C1-C6酰基团;苯甲酰基团或苯环;以及这些化合物的盐和/或活性代谢物。
  • Novel tricyclic spiropiperidines or spiropyrrolidines
    申请人:Hossain Nafizal
    公开号:US20050245741A1
    公开(公告)日:2005-11-03
    The invention provides compounds of formula (I) wherein m, R 1 , n, R 2 , q, X, Y, Z, R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , t and R 9 are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
    本发明提供了公式(I)的化合物,其中m、R1、n、R2、q、X、Y、Z、R3、R4、R5、R6、R7、R8、t和R9如规范中所定义,以及它们的制备方法、包含它们的制药组合物及其在治疗中的应用。
  • Benzisoxazole Compound
    申请人:Sasaki Atsushi
    公开号:US20090318690A1
    公开(公告)日:2009-12-24
    Disclosed is a compound represented by the general formula (I) or a salt thereof: wherein any one of R1, R2 and R3 represents a group represented by the formula: —(CH 2 )m-NR11R12 (wherein m is 1 or 2; and R11 and R12 independently represent a hydrogen atom or a C1-6 alkyl group or may, together with a nitrogen atom to which R11 and R12 are bound, form a 4- or 5-membered cyclic group); the remaining two or R1, R2 and R3 independently represent a group represented by the formula: —(O)n-R21 (wherein n is 0 or 1; and R21 represents a hydrogen atom, a C1-6 alkyl group, a C2-6 alkenyl group, a C2-6 alkynyl group, or the like); and R4 represents a C1-6 alkyl group which may have a substituent or the like.
    本发明涉及一种由通式(I)表示的化合物或其盐:其中R1、R2和R3中的任意一个表示公式表示的基团:—(CH2)m-NR11R12(其中m为1或2;R11和R12独立地表示氢原子或C1-6烷基或可能与R11和R12结合的氮原子一起形成4-或5-成员环状基团);剩余的两个或R1、R2和R3独立地表示公式表示的基团:—(O)n-R21(其中n为0或1;R21表示氢原子、C1-6烷基、C2-6烯基、C2-6炔基等);R4表示可能具有取代基的C1-6烷基。
  • Novel tricyclic spiroderivatives as modulators of chemokine receptor acitivity
    申请人:Hossain Nafizal
    公开号:US20070099945A1
    公开(公告)日:2007-05-03
    The invention provides compounds of formula (I) wherein m, R 1 , n, R 2 , q, p, X, Y, R 3 , R 4 , t and, R 5 are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
    该发明提供了式(I)的化合物,其中m,R1,n,R2,q,p,X,Y,R3,R4,t和R5如规范中定义,以及它们的制备方法,含有它们的制药组合物以及它们在治疗中的应用。
  • Novel tricyclic spiroderivatives as modulators of chemokine receptor activity
    申请人:Hossain Nafizal
    公开号:US20070021498A1
    公开(公告)日:2007-01-25
    The invention provides compounds of formula (I) wherein m, R 1 , n, R 2 , q, X, Y, Z, R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , t and R 9 are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
    该发明提供了式(I)的化合物,其中m,R1,n,R2,q,X,Y,Z,R3,R4,R5,R6,R7,R8,t和R9如规范中所定义,其制备方法,包含它们的制药组合物以及它们在治疗中的用途。
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