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3,5-dinitrophthalic anhydride | 52806-20-9

中文名称
——
中文别名
——
英文名称
3,5-dinitrophthalic anhydride
英文别名
3,5-Dinitro-phthalsaeure-anhydrid;4,6-dinitro-2-benzofuran-1,3-dione
3,5-dinitrophthalic anhydride化学式
CAS
52806-20-9
化学式
C8H2N2O7
mdl
——
分子量
238.113
InChiKey
BLSODAOHVLJUAT-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):
    1
  • 重原子数:
    17
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    135
  • 氢给体数:
    0
  • 氢受体数:
    7

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Aromatic nucleophilic substitution. Part 3. Preparation of novel 9-oxo-9H-thioxanthene- and 9-oxo-9H-xanthenedicarboximides and -dicarboxylates
    作者:Walter Fischer
    DOI:10.1002/hlca.19910740521
    日期:1991.8.7
    By aromatic nucleophilic substitution followed by intramolecular acylation, 9-oxo-9H-thioxanthene- and 9-oxo-9H-xanthene-dicarboximides were prepared from nitro- or chlorophthalimides and the dianions of thiosalicylic and salicylic acids (Scheme). The 9-oxo-9H-thioxanthene-3,4-dicarboximides were converted to 9-oxo-9H-thioxanthene-3,4-dicarboxylic-acid derivatives such as anhydride, esters, and further
    通过芳香亲核取代,接着通过分子内酰化,9-氧代-9- ħ -thioxanthene-和9-氧代-9- ħ呫吨二甲酰亚胺从硝基或chlorophthalimides和硫代水杨酸水杨酸的二价阴离子(其制备方案)。将9-氧代-9 H-氧杂蒽-3,4-二甲酰亚胺转化为9-氧代-9 H-氧杂蒽-3,4-二羧酸生物,例如酸酐,酯和其他酰亚胺。这些衍生物中的一些被证明是具有特殊性质的优异光敏剂,例如液体聚集形式,H 2 O溶解度,在亲脂性有机溶剂和聚合物中的溶解度或吸收波长的红移。
  • 3,5-Disubstituted phthalic acid imides, phthalic acids and phthalic acid
    申请人:Ciba-Geigy Corporation
    公开号:US04363917A1
    公开(公告)日:1982-12-14
    Novel compounds of the formula I or II ##STR1## are described, in which M.sub.1 and M.sub.2 individually are --OH or together are --O--, R is hydrogen, C.sub.1-20 -alkyl, C.sub.2-5 -alkenyl, C.sub.3-5 -alkynyl, C.sub.5-12 -cycloalkyl, benzyl, phenyl or toluyl, X is --NO.sub.2, --OR', --SR' or --SO.sub.2 R' and the (R')s independently of one another are C.sub.1-20 -alkyl, C.sub.3-5 -alkenyl, C.sub.3-5 -alkynyl, C.sub.2-4 -monohydroxyalkyl, C.sub.1-12 -halogenoalkyl, benzyl, C.sub.5-12 -cycloalkyl, phenyl, carboxyphenyl, halogenophenyl, nitrophenyl, alkyl- or alkoxy-phenyl each having 1-4 C atoms in the alkyl or alkoxy moieties, or acetylaminophenyl. The compounds (I) and compounds (II) in which M.sub.1 and M.sub.2 together are --O-- are suitable as sensitizers for photocrosslinkable polymers or as initiators for the photopolymerization of ethylenically unsaturated compounds or for the photochemical crosslinking of polyolefins.
    描述了公式I或II的新化合物,其中M.sub.1和M.sub.2分别为--OH或者一起为--O--,R为氢,C.sub.1-20-烷基,C.sub.2-5-烯基,C.sub.3-5-炔基,C.sub.5-12-环烷基,苄基,苯基或甲苯基,X为--NO.sub.2,--OR',--SR'或--SO.sub.2 R',而(R')s独立地为C.sub.1-20-烷基,C.sub.3-5-烯基,C.sub.3-5-炔基,C.sub.2-4-单羟基烷基,C.sub.1-12-卤代烷基,苄基,C.sub.5-12-环烷基,苯基,羧基苯基,卤代苯基,硝基苯基,烷基或烷氧基苯基,其中烷基或烷氧基中每个有1-4个碳原子,或乙酰基苯基。其中M.sub.1和M.sub.2一起为--O--的化合物(I)和化合物(II)可用作光交联聚合物的感光剂,或用作乙烯不饱和化合物的光聚合引发剂,或用于聚烯烃的光化学交联。
  • Thioxanthonecarboxylic acids and thioxanthonecarboxylic acid derivatives
    申请人:Ciba-Geigy Corporation
    公开号:US04385182A1
    公开(公告)日:1983-05-24
    Novel thioxanthonecarboxylic acids and thioxanthonecarboxylic acid derivatives of the formula I ##STR1## in which Y is --COOH, --CO-halogen, --CN or a carboxylic acid ester, thioester or amide group and X, Z and W are as defined in the patent claim, are described. The compounds of the formula I in which Y is other than --CO--halogen are suitable as sensitizers for photo-crosslinkable polymers or as initiators for photo-polymerization of ethylenically unsaturated compounds or for photo-chemical crosslinking of polyolefins. The acid halides of the formula I are starting materials for the preparation of the corresponding nitriles and carboxylic acid esters, thioesters and amides.
    新型噻吩羧酸噻吩羧酸生物化学式I ##STR1## 其中Y为--COOH,--CO-卤素,--CN或羧酸酯,酯或酰胺基团,而X、Z和W如专利要求中所定义。化学式I中Y不是--CO--卤素的化合物适用于作为光交联聚合物的增感剂,或作为乙烯不饱和化合物的光聚合引发剂,或用于聚烯烃的光化学交联。化学式I的酸卤是制备相应的腈和羧酸酯,酯和酰胺的起始材料。
  • Aromatic Nucleophilic Substitution. Part 1. Regiospecific Substitution of the Nitro Groups in 3,5-Dinitrophthalic-Acid Derivatives
    作者:Walter Fischer、Vratislav Kvita
    DOI:10.1002/hlca.19850680405
    日期:1985.6.26
    The regioselectivity of nucleophilic substitution of the nitro groups in 3,5-dinitrophthalic anhydrides and 3,5-dinitrophthalimides (Scheme) with a variety of nucleophiles (Nu−) was studied. In all cases, the 3-nitro group was selectively substituted. With excess of the same nucleophilic reagent or with other nucleophiles, the 5-nitro group could subsequently be replaced.
    在硝基基团的亲核取代的3,5- dinitrophthalic酸酐和3,5- dinitrophthalimides(区域选择性方案)与各种亲核试剂的(女- )进行了研究。在所有情况下,3-硝基均被选择性取代。在过量的相同亲核试剂或其他亲核试剂的情况下,随后可以取代5-硝基。
  • 3,5-Disubstituted phthalic acids and phthalic anhydrides
    申请人:Ciba-Geigy Corporation
    公开号:US04480105A1
    公开(公告)日:1984-10-30
    Novel compounds of the formula II ##STR1## are described, in which M.sub.1 and M.sub.2 individually are --OH or together are --O--, X is --NO.sub.2, --OR', --SR' or SO.sub.2 R' and the (R')s independently of one another are C.sub.1-20 -alkyl, C.sub.3-5 -alkenyl, C.sub.3-5 -alkynyl, C.sub.2-4 -monohydroxyalkyl, C.sub.1-12 -halogenoalkyl, benzyl, C.sub.5-12 -cycloalkyl, phenyl, carboxyphenyl, halogenophenyl, nitrophenyl, alkyl- or alkoxy-phenyl each having 1-4 C atoms in the alkyl or alkoxy moieties, or acetylaminophenyl, such as for example 3-n-butylthio-5-nitrophthalic anhydride. The compounds (II) in which M.sub.1 and M.sub.2 together are --O-- are suitable as sensitizers for photo-crosslinkable polymers or as initiators for the photopolymerization of ethylenically unsaturated compounds or for the photochemical crosslinking of polyolefins, and those where M.sub.1 and M.sub.2 are --OH are useful intermediates for those wherein M.sub.1 and M.sub.2 together are --O--.
    本发明涉及式II的新化合物,其中M1和M2分别为--OH或共同为--O--,X为--NO2,--OR',--SR'或SO2R',而(R')各自独立地为C1-20烷基,C3-5烯基,C3-5炔基,C2-4单羟基烷基,C1-12卤代烷基,苄基,C5-12环烷基,苯基,羧基苯基,卤代苯基,硝基苯基,烷基或烷氧基苯基,其中烷基或烷氧基中的烷基或烷氧基中含有1-4个C原子,或乙酰基苯基,例如3-正丁基-5-硝基邻苯二酐。其中M1和M2共同为--O--的化合物(II)适用于光交联聚合物的敏化剂,或用于乙烯基不饱和化合物的光聚合或用于聚烯烃的光化学交联,而M1和M2为--OH的化合物则是M1和M2共同为--O--的化合物的有用中间体。
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同类化合物

()-2-(5-甲基-2-氧代苯并呋喃-3(2)-亚乙基)乙酸乙酯 顺式-1-((2-(5-氯-2-苯并呋喃基)-4-甲基-1,3-二氧戊环-2-基)甲基)-1H-1,2,4-三唑 顺式-1-((2-(5,7-二氯-2-苯并呋喃基)-4-乙基-1,3-二氧戊环-2-基)甲基)-1H-咪唑 顺式-1-((2-(2-苯并呋喃基)-4-乙基-1,3-二氧戊环-2-基)甲基)-1H-1,2,4-三唑 霉酚酸酯杂质B 雷美替胺杂质3 雷美替胺杂质22 雷美替胺杂质 间甲酚紫 间甲基苯基(苯并呋喃-2-基)甲醇 长管假茉莉素C 钠1,4-二[(2-乙基己基)氧基]-1,4-二氧代-2-丁烷磺酸酯-3,3-二(4-羟基苯基)-2-苯并呋喃-1(3H)-酮(1:1:1) 金霉素 酪氨酸,b-羰基- 酞酸酐-d4 酚酞二丁酸酯 酚酞 酚红钠 酚红 邻苯二甲酸酐与马来酸酐,甘氨酰蜡素和二乙二醇的聚合物 邻苯二甲酸酐与己二醇的聚合物 邻苯二甲酸酐与三甘醇异壬醇的聚合物 邻苯二甲酸酐与2-乙基-2-羟甲基-1,3-丙二醇和2,5-呋喃二酮的聚合物 邻苯二甲酸酐与2-乙基-2-羟甲基-1,3-丙二醇、2,5-呋喃二酮和2-乙基己酸苯甲酸酯的聚合物 邻苯二甲酸酐-13C6 邻苯二甲酸酐-4-硼酸频哪醇酯 邻苯二甲酸酐,马来酸,二乙二醇,新戊二醇聚合物 邻甲酚酞二庚酸酯 邻甲酚酞二己酸酯 邻甲酚酞 贝康唑 表灰黄霉素 螺佐呋酮 螺[苯并呋喃-3(2H),4-哌啶] 螺[异苯并呋喃-1(3H),4’-哌啶]-3-酮 螺[异苯并呋喃-1(3H),4'-哌啶]-3-酮盐酸盐 螺[异苯并呋喃-1(3H),3’-吡咯烷]-3-酮 螺[1-苯并呋喃-2,1'-环丙烷]-3-酮 薄荷内酯 萘并[2,3-b]呋喃-8(4H)-酮,4a,5,6,7,8a,9-六氢-,顺- 莫罗卡尼 荨麻叶泽兰酮 荧光胺 苯酞-3-乙酸 苯酚,2-[3-(2-苯并呋喃基)-5,6-二氢-1,2,4-三唑并[3,4-b][1,3,4]噻二唑-6-基]- 苯酐二乙二醇共聚物 苯酐 苯甲酸,2-[(1,3-二羰基丁基)氨基]-,甲基酯 苯甲酸,2,2-二(羟甲基)丙烷-1,3-二醇,异苯并呋喃-1,3-二酮 苯甲酰氯化,3-甲氧基-4-甲基-