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1,4-二苄基苯 | 793-23-7

中文名称
1,4-二苄基苯
中文别名
——
英文名称
1,4-dibenzylbenzene
英文别名
p-dibenzylbenzene;1,4-bis(phenylmethyl)benzene
1,4-二苄基苯化学式
CAS
793-23-7
化学式
C20H18
mdl
MFCD00094396
分子量
258.363
InChiKey
LTGXPINWZFIICV-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:
    87.5°C
  • 沸点:
    336.61°C (rough estimate)
  • 密度:
    1.0524 (estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    6.1
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

SDS

SDS:30c0078a4e4990063dc294e3d845e0ec
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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

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文献信息

  • Para—or meso-functionalized aromatic ketone compounds, preparation methods thereof, and photopolymerization initiators comprising the same
    申请人:Zhang Yongbo
    公开号:US08742175B2
    公开(公告)日:2014-06-03
    The present invention discloses novel aromatic ketone compounds with functional substitution groups at para- or meta positions which can be used as photo-initiators or effective components of photo-initiator mixtures for the photopolymerizations of ethylenically unsaturated systems. The preparation of these compounds is also disclosed.
    本发明公开了新颖的芳香酮化合物,其在对位或间位具有功能性取代基,可用作乙烯基不饱和体系光聚合的光引发剂或光引发剂混合物的有效成分。这些化合物的制备方法也一并公开。
  • Palladium catalyzed ligand-free Suzuki cross-coupling reactions of benzylic halides with aryl boronic acids under mild conditions
    作者:B.P. Bandgar、Sampada V. Bettigeri、Jaywant Phopase
    DOI:10.1016/j.tetlet.2004.07.073
    日期:2004.9
    A highly efficient Suzuki cross-coupling reaction between benzylic halides and aryl boronic acids using palladium chloride as catalyst in acetone:water (3:1) as the solvent system has been developed. High yields of products, mild reaction conditions and short reaction times in the absence of ligand are important features of this method.
    在丙酮:水(3∶1)作为溶剂体系中,使用氯化钯作为催化剂,开发了苄基卤化物和芳基硼​​酸之间的高效铃木交叉偶联反应。该方法的重要特征是产物的高收率,温和的反应条件和在不存在配体的情况下较短的反应时间。
  • Selective electrochemical oxidation of aromatic hydrocarbons and preparation of mono/multi-carbonyl compounds
    作者:Zhibin Li、Yan Zhang、Kuiliang Li、Zhenghong Zhou、Zhenggen Zha、Zhiyong Wang
    DOI:10.1007/s11426-021-1061-x
    日期:2021.12
    A selective electrochemical oxidation was developed under mild condition. Various mono-carbonyl and multi-carbonyl compounds can be prepared from different aromatic hydrocarbons with moderate to excellent yield and selectivity by virtue of this electrochemical oxidation. The produced carbonyl compounds can be further transformed into α-ketoamides, homoallylic alcohols and oximes in a one-pot reaction
    在温和条件下开发了选择性电化学氧化。凭借这种电化学氧化,可以从不同的芳烃以中等至优异的产率和选择性制备各种单羰基和多羰基化合物。生成的羰基化合物可以在一锅反应中进一步转化为α-酮酰胺、高烯丙醇和肟。特别是,在单锅连续电解中制备了一系列 α-酮酰胺。机理研究表明,2,2,2-trifluoroethan-1-ol (TFE) 可以与催化剂物种相互作用并生成相应的氢键配合物,以提高电化学氧化性能。
  • Convulsive Status Epilepticus in Children with Intractable Epilepsy is Frequently Focal in Origin
    作者:Mohammed M.S. Jan、Brian G.R. Neville、Timothy C. Cox、Rod C. Scott
    DOI:10.1017/s0317167100001748
    日期:2002.2
    Background:

    Convulsive status epilepticus (CSE) is a common neurological emergency. Our objectives were to study children with recurrent nonfebrile CSE to assess the evidence for focal origin.

    Methods:

    Series of 18 children with recurrent CSE and intractable epilepsy were identified by chart review. Clinical, radiological, and EEG data were reviewed. Focal structural abnormalities were identified on MRI and CT images by one neuroradiologist who was unaware of the clinical details.

    Results:

    The patient's ages ranged between 6-22 years (mean 15.3, SD 4), and 67% were males. Most children (89%) had a severe cognitive and / or behavioural disorder. Most patients (89%) had multiple seizure types and 95% of these were partial seizures. Twelve (67%) children had at least one episode of CSE with focal features identified clinically. Focal brain abnormalities were detected on 18% and 55% of CTand MRI films respectively. Overall, 53% had a focal abnormality on structural neuroimaging. Interictal EEG revealed focal or multifocal abnormalities on at least one occasion in 94% and 22% of patients respectively. Overall, 17 patients had focal features on at least one EEG. Thirteen ictal EEGs were recorded on 11 (61%) patients. Ten (91%) of these recordings revealed a focal onset.

    Conclusions:

    Many handicapped children with recurrent CSE have focal clinical, radiological, or electrographic features. This supports a focal origin for CSE in most children with intractable epilepsy.

    背景:惊厥性癫痫状态(CSE)是一种常见的神经系统急症。我们的目的是研究反复发作的非发热性CSE患儿,以评估病灶起源的证据。方法:通过病历审查确定了18名反复发作的CSE和难治性癫痫患儿。回顾了临床、放射学和脑电图数据。结果:患者年龄在6-22岁之间(平均15.3岁,SD为4),67%为男性。大多数儿童(89%)患有严重的认知和/或行为障碍。大多数患者(89%)有多种癫痫发作类型,其中 95% 为部分性癫痫发作。12名患儿(67%)至少有一次CSE发作,临床上发现其具有局灶性特征。分别有 18% 和 55% 的 CT 和核磁共振成像片检测到局灶性脑部异常。总体而言,53%的患儿在神经结构影像学检查中发现局灶性异常。分别有 94% 和 22% 的患者在发作间期脑电图上发现至少一次局灶性或多灶性异常。总体而言,17 名患者至少有一次脑电图出现局灶性特征。11 名患者(61%)记录了 13 次发作期脑电图。结论:许多复发性 CSE 的残障儿童具有局灶性临床、放射学或电图特征。这支持了大多数难治性癫痫患儿的CSE起源于病灶。
  • Friedel-Crafts Benzylation of Arenes over Mixed Oxides
    作者:Sujit R. Jadhav、Manohar R. Sawant
    DOI:10.1002/jccs.200400021
    日期:2004.2
    The replacement of liquid acid catalyst by solid acids for the Friedel-Crafts reaction of aromatic alkylation is a challenging task. Mixed oxide possessing spinel structures were found to catalyze the Friedel-Craft benzylation of arenes. It was found that the reaction was very fast at 80 °C, hence the reaction was studied with respect to more substrate. The significant point was even at this temperature
    用固体酸代替液体酸催化剂用于芳族烷基化的傅克反应是一项具有挑战性的任务。发现具有尖晶石结构的混合氧化物催化芳烃的傅-克苄基化。发现反应在 80 °C 时非常快,因此研究了更多底物的反应。重要的一点是即使在该温度下也实现了以对位异构体为主的单苄基化。采用共沉淀法制备混合氧化物,并采用XRD技术对其进行表征。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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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