摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2,3,4,5-四氯-6-氰基苯甲酸甲酯 | 5358-06-5

中文名称
2,3,4,5-四氯-6-氰基苯甲酸甲酯
中文别名
——
英文名称
3,4,5,6-tetrachloro-2-cyanobenzoic acid methyl ester
英文别名
3,4,5,6-tetrachloro-o-cyanobenzoic acid methyl ester;3,4,5,6-tetrachlorocyanobenzoic acid methyl ester;methyl 3,4,5,6-tetrachloro-2-cyanobenzoate;methyl 3,4,5,6-tetrachloro-o-cyanobenzoate;methyl 2,3,4,5-tetrachloro-6-cyanobenzoate;tetrachloro-o-cyanobenzoic acid methyl ester
2,3,4,5-四氯-6-氰基苯甲酸甲酯化学式
CAS
5358-06-5
化学式
C9H3Cl4NO2
mdl
——
分子量
298.94
InChiKey
XYQXGZLLGNQFSL-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

  • 熔点:
    83-84 °C
  • 沸点:
    394.4±42.0 °C(Predicted)
  • 密度:
    1.65±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    50.1
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2926909090

SDS

SDS:5bb8afbe6f3e478f2cfb97652cd08139
查看

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

反应信息

  • 作为反应物:
    描述:
    2,3,4,5-四氯-6-氰基苯甲酸甲酯 生成 methyl 2-cyano-3,4,5,6-tetrafluorobenzoate
    参考文献:
    名称:
    HACKENBRUCH, JOACHIM;PAPENFUHS, THEODOR
    摘要:
    DOI:
  • 作为产物:
    描述:
    sodium salt of tetrachloro-2-cyanobenzoic acid 生成 2,3,4,5-四氯-6-氰基苯甲酸甲酯
    参考文献:
    名称:
    VON, DER CRONE JOST;OVERNEY, GONZAQUE;DARIO, PETER
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • [EN] PROCESS FOR THE PREPARATION OF ORGANIC PIGMENTS<br/>[FR] PROCEDE DE PREPARATION DE PIGMENTS ORGANIQUES
    申请人:MCA TECHNOLOGIES GMBH
    公开号:WO2005085364A1
    公开(公告)日:2005-09-15
    The present invention relates to advantageous processes for the manufacture of organic pigments and their precursors. The invention particularly relates to reactions carried out in an 'All In One Reactor'® (Draiswerke GmbH, Germany), a kneader like the TurbuKneader® of the same company, a paddle dryer like the Turbudry® of the same company or a related system and thereby submitting the reaction mixtures to enhanced driving power as expressed by a Froude number>1, the reaction mixture being caused to react in high concentrations at elevated temperature.
    本发明涉及有利的有机颜料及其前体制造过程。该发明特别涉及在“全能反应器”®(德国Draiswerke GmbH公司)、类似于同一公司的TurbuKneader®的搅拌器、类似于同一公司的Turbudry®的搅拌干燥器或相关系统中进行的反应,从而通过Froude数>1表达的增强驱动力使反应混合物在高浓度和高温下发生反应。
  • Process for the preparation of alkyl esters of
    申请人:Ciba-Geigy Corporation
    公开号:US04978768A1
    公开(公告)日:1990-12-18
    Tetrachloro-2-cyanobenzoic acid alkyl esters of formula ##STR1## wherein R is C.sub.1 -C.sub.5 alkyl, can be very conveniently prepared by (a) reacting the ammonium salt of tetrachloro-2-cyanobenzoic acid, in the presence of water and an inert organic solvent, with a hydroxide of formula MOH, wherein M is Na or K, and removing the ammonia evolved, and (b) reacting the resultant salt of the formula ##STR2## wherein M is as defined above, with at least 1 mole of a dialkyl sulfate of formula SO.sub.2 (OR).sub.2 or an alkyl halide of formula RHal, wherein R is as defined above and Hal is Cl, Br, I or F, also in the presence of water and an inert organic solvent.
    式为##STR1##的四氯-2-氰基苯甲酸烷基酯,其中R为C.sub.1-C.sub.5烷基,可以通过以下方法方便地制备:(a)在水和惰性有机溶剂的存在下,将四氯-2-氰基苯甲酸铵盐与式为MOH的氢氧化物反应,其中M为Na或K,并去除放出的氨,(b)在水和惰性有机溶剂的存在下,将所得的式为##STR2##的盐与至少1摩尔的式为SO.sub.2(OR).sub.2的二烷基硫酸酯或式为RHal的烷基卤化物反应,其中R如上所定义,Hal为Cl、Br、I或F。
  • Azomethine pigments
    申请人:Ciba-Geigy Corporation
    公开号:US04024132A1
    公开(公告)日:1977-05-17
    Azomethine pigments of the formula ##STR1## and metal complexes thereof, wherein A denotes an isocyclic or heterocyclic aromatic radical, R denotes a H atom, an alkyl group containing 1-6 C atoms, or an aryl radical, X.sub.2 and X.sub.4 denote H atoms or halogen atoms, X.sub.1 and X.sub.3 denote H atoms or halogen atoms, alkoxy or alkylmercapto groups containing 1-6 C atoms, cycloalkoxy groups containing 5-6 C atoms, or aralkoxy, aryloxy or arylmercapto groups, it being possible for one of the substituents X.sub.1 -X.sub.4 also to be a nitro group which are useful for pigmenting of high molecular material.
    式子为##STR1##的偶氮亚胺颜料及其金属配合物,其中A表示异环或杂环芳基,R表示氢原子,含有1-6个C原子的烷基或芳基基团,X.sub.2和X.sub.4表示氢原子或卤素原子,X.sub.1和X.sub.3表示氢原子或卤素原子,含有1-6个C原子的烷氧基或烷硫基基团,含有5-6个C原子的环烷氧基基团,或者芳基氧基、芳基硫基或芳烷氧基基团,其中X.sub.1-X.sub.4的取代基中可以有一个是硝基,该颜料适用于高分子材料的着色。
  • Process for the Preparation of Organic Materials
    申请人:KAUL Bansi Lal
    公开号:US20090017307A1
    公开(公告)日:2009-01-15
    The present invention relates to advantageous processes for the manufacture of organic pigments and their precursors. The invention particularly relates to reactions carried out in an “All In One Reactor”® (Draiswerke GmbH, Germany), a kneader like the TurbuKneader® of the same company, a paddle dryer like the Turbudry® of the same company or a related system and thereby submitting the reaction mixtures to enhanced driving power as expressed by a Froude number >1, the reaction mixture being caused to react in high concentrations at elevated temperature.
    本发明涉及有利的有机颜料及其前体制造工艺。该发明特别涉及在“全自动反应器”®(德国Draiswerke GmbH公司)、类似于该公司的TurbuKneader®的搅拌器、类似于该公司的Turbudry®的刮板干燥器或相关系统中进行的反应,并通过弗洛德数>1表达的增强驱动力将反应混合物在高浓度和高温下反应。
  • Process for the preparation of organic materials
    申请人:Kaul Lal Bansi
    公开号:US20070119345A1
    公开(公告)日:2007-05-31
    The present invention relates to advantageous processes for the manufacture of organic pigments and their precursors. The invention particularly relates to reactions carried out in an “All In One Reactor”® (Draiswerke GmbH, Germany), a kneader like the TurbuKneader® of the same company, a paddle dryer like the Turbudry® of the same company or a related system and thereby submitting the reaction mixtures to enhanced driving power as expressed by a Froude number >1, the reaction mixture being caused to react in high concentrations at elevated temperature.
    本发明涉及有机颜料及其前体的制造的优越工艺。特别是,本发明涉及在“全过程反应器”®(德国Draiswerke GmbH公司)、类似于该公司的TurbuKneader®的搅拌器、类似于该公司的Turbudry®的刮板干燥器或相关系统中进行的反应,并通过弗洛德数>1表达的增强驱动功率使反应混合物在高浓度和高温下反应。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐