2,3,4,2'-tetrahydroxy-benzophenone | 42204-63-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2,3,4,2'-tetrahydroxy-benzophenone
• 英文别名: 2,3,4,2'-Tetrahydroxy-benzophenon；(2-hydroxyphenyl)(2,3,4-trihydroxyphenyl)-methanone；2,2',3,4-tetrahydroxybenzophenone；(2-Hydroxyphenyl)(2,3,4-trihydroxyphenyl)methanone；(2-hydroxyphenyl)-(2,3,4-trihydroxyphenyl)methanone
• CAS: 42204-63-7
• 化学式: C₁₃H₁₀O₅
• 分子量: 246.219
• InChiKey: APVNRHLATFVPPS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  98
• 氢给体数：
  4
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2,3,4,2'-tetrahydroxy-benzophenone 在 sodium acetate 作用下， 以 水 为溶剂， 反应 0.2h， 以96%的产率得到3,4-二羟基氧杂蒽酮
  参考文献：
  名称：

  Microwave-Assisted Efficient and Green Synthesis of Hydroxyxanthone in Water

  摘要：

  An efficient and green procedure has been developed for the synthesis of hydroxyxanthones from substituted 2,2'-dihydroxybenzophenone precursors via microwave-assisted base-catalyzed cyclization in water. This method provides excellent yields of products in a short time, making it a useful strategy for the synthesis of structurally diverse hydroxyxanthones.

  DOI：

  10.1080/00397911.2011.573170
• 作为产物：
  描述：

  2-乙酸基苯甲腈 、 邻苯三酚 在 盐酸 、 乙醚 、 zinc(II) chloride 作用下， 生成 2,3,4,2'-tetrahydroxy-benzophenone
  参考文献：
  名称：

  Atkinson; Heilbron, Journal of the Chemical Society, 1926, p. 2690

  摘要：

  DOI：

文献信息

• Evaluation of Polyhydroxybenzophenones as α-Glucosidase Inhibitors
  作者：Xuesen Hu、Yang Xiao、Jianlong Wu、Lin Ma

  DOI：10.1002/ardp.201000147

  日期：2011.2

  This experiment was designed to synthesize 18 kinds of polyhydroxybenzophenones by using Friedel‐Crafts reaction, and to measure the inhibitory activity on α‐glucosidase with p‐nitrophenyl‐β‐D‐galactopyranoside (PNPG) as a substrate. Here, acarbose (IC50 = 1674.75 µmol L−1) was used as the reference inhibitor. The results demonstrated that most of the target compounds had remarkable inhibitory activities

  本实验旨在利用Friedel-Crafts反应合成18种多羟基二苯甲酮，以对硝基苯基-β-D-吡喃半乳糖苷（PNPG）为底物，测定对α-葡萄糖苷酶的抑制活性。在这里，阿卡波糖 (IC50 = 1674.75 µmol L - 1) 用作参考抑制剂。结果表明，大多数目标化合物对α-葡萄糖苷酶具有显着的抑制活性。在所有这些化合物中，2,4,4', 6-butahydroxydiphenylketone (11) 被发现是最有效的 α-葡萄糖苷酶抑制剂，IC50 值为 10.62 µmol L - 1。此外，我们通过动力学分析发现这些化合物是竞争性抑制剂。结果表明，此类化合物可用于开发新的糖尿病治疗候选药物。
• [EN] LATENT ACIDS AND THEIR USE<br/>[FR] ACIDES LATENTS ET LEUR UTILISATION
  申请人：BASF SE

  公开号：WO2016124493A1

  公开（公告）日：2016-08-11

  Compounds of the formula (I) and (IA) wherein X is -O(CO)-; R1 is C1-C12haloalkyl or C6-C10haloaryl; R2 is located in position 7 of the coumarinyl ring and is OR8; R2a, R2b and R2C independently of each other are hydrogen; R3 is C1-C8haloalkyl or C1-C8haloalkyl; R4 is hydrogen; and R8 is C1-C6alkyI; are suitable as photosensitive acid donors in the preparation of photoresist compositions such as used for example in the preparation of spacers, insulating layers, interlayer dielectric films, insulation layers, planarization layers, protecting layers, overcoat layers, banks for electroluminescence displays and liquid crystal displays (LCD).

  化合物的化学式（I）和（IA），其中X为-O(CO)-；R1为C1-C12卤代烷基或C6-C10卤代芳基；R2位于香豆素环的第7位，为OR8；R2a、R2b和R2C彼此独立地为氢；R3为C1-C8卤代烷基或C1-C8卤代烷基；R4为氢；R8为C1-C6烷基，适用于作为感光酸给体，用于制备光刻胶组合物，例如用于制备间隔层、绝缘层、层间介质膜、绝缘层、平坦化层、保护层、覆盖层、电致发光显示器和液晶显示器（LCD）的制备。
• [EN] SULFONIUM DERIVATIVES AND THE USE THEROF AS LATENT ACIDS<br/>[FR] DÉRIVÉS DE SULFONIUM ET LEUR UTILISATION EN TANT QU'ACIDES LATENTS
  申请人：BASF SE

  公开号：WO2010046240A1

  公开（公告）日：2010-04-29

  Compounds of the formula (I), wherein Ar1 is for example phenylene or biphenylene both unsubstituted or substituted; Ar2 and Ar3 are for example independently of each other phenyl, naphthyl, biphenylylyl or heteroaryl, all optionally substituted; or Ar1 and Ar2 for example together with a direct bond, O, S or (CO), form a fused ring system; R is for example hydrogen, C3-C30cycloalkyl or C1-C18alkyl; and R1, R2 and R3 independently of each other are for example C1-C10haloalkyl; are effective photoacid generators (PAG).

  化合物的公式（I），其中Ar1例如是未取代或取代的苯基或联苯基; Ar2和Ar3例如是独立的苯基，萘基，联苯基或杂环基，均可选取代; 或者例如Ar1和Ar2与直接键，O，S或（CO）一起形成融合的环系统; R例如是氢，C3-C30环烷基或C1-C18烷基; R1，R2和R3独立地例如是C1-C10卤代烷基; 是有效的光酸发生剂（PAG）。
• SULFONIUM COMPOUNDS, THEIR PREPARATION AND USE
  申请人：BASF SE

  公开号：US20150044509A1

  公开（公告）日：2015-02-12

  Compounds of the formula (I), (Ia) or (Ib) wherein A 1 , and A − is for example (II) is 1 or 2; X is C 1 -C 4 alkylene or CO; Y is for example O, O(CO), O(CO)O, R 1 is for example hydrogen, d-dsalkyl, C 3 -C 30 cycloalkyl, phenyl, naphthyl, anthracyl, phenanthryl, biphenylyl, fluorenyl or C 3 -C 20 heteroaryl, all of which optionally are substituted; R 2 and R 3 for example are C 1 -C 10 haloalkylene which is optionally substituted, or R 2 and R 3 are phenylene, which optionally is substituted; R 4 is a group (A) or a group (B); R 5 and R 6 for example are C 1 -C 20 alkyl; or R 4 and R 5 or R 4 and R 6 together form a straight-chain C 2 -C 6 alkylene, R 5 and R 6 together form a straight-chain C 2 -C 6 alkylene; R 7 , R 8 , R 9 and R 10 ifor example are C 1 -C 20 alkyl; M for example is C 1 -C 20 alkylene, C 2 -C 20 alkenylene, C 2 -C 20 alkynylene; R 25 and R 26 are for example hydrogen, C 1 -C 20 alkyl; R 27 , R 28 , R 29 , R 30 and R 31 are for example hydrogen, C 1 -C 20 alkyl, C 2 -C 20 alkenyl, C 3 -C 20 cycloalkyl, or two radicals R 27 and R 28 , R 28 and R 29 , R 29 and R 30 and/or R 30 and R 31 together form a straight-chain C 2 -C 6 alkylene, or R 25 and R 27 together form 1,2-phenylene, R 33 and R 34 for example are hydrogen, C 1 -C 20 alkyl; R 35 , R 36 and R 37 for example are hydrogen, C 1 -C 20 alkyl; are suitable as thermo-acid generators.

  化合物的公式(I)、(Ia)或(Ib)，其中A1和A-例如(II)为1或2；X为C1-C4烷基或CO；Y例如为O、O(CO)、O(CO)O、R1例如为氢、d-ds烷基、C3-C30环烷基、苯基、萘基、蒽基、菲基、联苯基、芴基或C3-C20杂环芳基，全部可选地被取代；R2和R3例如为可选地被取代的C1-C10卤代烷基，或R2和R3为苯基，可选地被取代；R4为(A)基团或(B)基团；R5和R6例如为C1-C20烷基；或R4和R5或R4和R6一起形成直链C2-C6烷基，R5和R6一起形成直链C2-C6烷基；R7、R8、R9和R10例如为C1-C20烷基；M例如为C1-C20烷基、C2-C20烯基、C2-C20炔基；R25和R26例如为氢、C1-C20烷基；R27、R28、R29、R30和R31例如为氢、C1-C20烷基、C2-C20烯基、C3-C20环烷基，或两个基团R27和R28、R28和R29、R29和R30和/或R30和R31一起形成直链C2-C6烷基，或R25和R27一起形成1,2-苯基，R33和R34例如为氢、C1-C20烷基；R35、R36和R37例如为氢、C1-C20烷基；适用于热酸发生器。
• Latent acids and their use
  申请人：Yamato Hitoshi

  公开号：US20110217654A1

  公开（公告）日：2011-09-08

  The invention pertains to a compound generating an acid of the formula I or II, for instance corresponding sulfonium and iodonium salts, as well as corresponding sulfonyloximes wherein X is CH 2 or CO; Y is O, NR 4 , S, O(CO), O(CO)O, O(CO)NR 4 , OSO 2 , O(CS), or O(CS)NR 4 ; R 1 is for example C 1 -C 18 alkyl, C 1 -C 10 haloalkyl, C 2 -C 12 alkenyl, C 4 -C 30 cycloalkenyl, phenyl-C 1 -C 3 -alkyl, C 3 -C 30 cycloalkyl, C 3 -C 30 cycloalkyl-C 1 -C 18 alkyl, interrupted C 2 -C 18 alkyl, interrupted C 3 -C 30 cycloalkyl, interrupted C 3 -C 30 cycloalkyl-C 1 -C 18 alkyl, interrupted C 4 -C 30 cycloalkenyl, phenyl, naphthyl, anthracyl, phenanthryl, biphenylyl, fluorenyl or heteroaryl, all unsubstituted or are substituted; or R 1 is NR 12 R 13 ; R 2 and R 3 are for example C 3 -C 30 cycloalkylene, C 3 -C 30 cycloalkyl-C 1 -C 18 alkylene, C 1 -C 18 alkylene, C 1 -C 10 haloalkylene, C 2 -C 12 alkenylene, C 4 -C 30 cycloalkenylene, phenylene, naphthylene, anthracylene, phenanthrylene, biphenylene or heteroarylene; all unsubstituted or substituted; R 4 is for example C 3 -C 30 cycloalkyl, C 3 -C 30 cycloalkyl-C 1 -C 18 alkyl, C 1 -C 18 alkyl, C 1 -C 10 haloalkyl, C 2 -C 12 alkenyl, C 4 -C 30 cycloalkenyl, phenyl-C 1 -C 3 -alkyl; R 12 and R 13 are for example C 3 -C 30 cycloalkyl, C 3 -C 30 cycloalkyl-C 1 -C 18 alkyl, C 1 -C 18 alkyl, C 1 -C 10 haloalkyl, C 2 -C 12 alkenyl, C 4 -C 30 cycloalkenyl, phenyl-C 1 -C 3 -alkyl, Ar, (CO)R 15 , (CO)OR 15 or SO 2 R 15 ; and Ar is phenyl, biphenylyl, fluorenyl, naphthyl, anthracyl, phenanthryl or heteroaryl, all unsubstituted or substituted.

  本发明涉及一种生成公式I或II的酸的化合物，例如对应的磺鎓盐和碘鎓盐，以及对应的磺酰氧肟，其中X为CH2或CO；Y为O、NR4、S、O（CO）、O（CO）O、O（CO）NR4、OSO2、O（CS）或O（CS）NR4；R1例如为C1-C18烷基、C1-C10卤代烷基、C2-C12烯基、C4-C30环烯基、苯基-C1-C3-烷基、C3-C30环烷基、C3-C30环烷基-C1-C18烷基、中断的C2-C18烷基、中断的C3-C30环烷基、中断的C3-C30环烷基-C1-C18烷基、中断的C4-C30环烯基、苯基、萘基、蒽基、菲基、苯并二氢呋喃基或杂环基，全部未取代或被取代；或R1为NR12R13；R2和R3例如为C3-C30环烷基、C3-C30环烷基-C1-C18烷基、C1-C18烷基、C1-C10卤代烷基、C2-C12烯基、C4-C30环烯基、苯基、萘基、蒽基、菲基、苯并二氢呋喃基或杂环基，全部未取代或被取代；R4例如为C3-C30环烷基、C3-C30环烷基-C1-C18烷基、C1-C18烷基、C1-C10卤代烷基、C2-C12烯基、C4-C30环烯基、苯基-C1-C3-烷基；R12和R13例如为C3-C30环烷基、C3-C30环烷基-C1-C18烷基、C1-C18烷基、C1-C10卤代烷基、C2-C12烯基、C4-C30环烯基、苯基-C1-C3-烷基、Ar、（CO）R15、（CO）OR15或SO2R15；Ar为苯基、苯并二氢呋喃基、菲基、萘基、蒽基、苯并蒽基或杂环基，全部未取代或被取代。