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1-bromo-1-cyanoacetophenone | 35977-95-8

中文名称
——
中文别名
——
英文名称
1-bromo-1-cyanoacetophenone
英文别名
2-Bromo-3-oxo-3-phenylpropionitrile;2-bromo-3-oxo-3-phenylpropanenitrile
1-bromo-1-cyanoacetophenone化学式
CAS
35977-95-8
化学式
C9H6BrNO
mdl
——
分子量
224.057
InChiKey
KMQDAYBDKOKVNY-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

  • 沸点:
    289.8±25.0 °C(Predicted)
  • 密度:
    1.551±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    12
  • 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:
    40.9
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:0ca2048f2a81b8a47f9daee2326c0819
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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

反应信息

  • 作为反应物:
    描述:
    1-bromo-1-cyanoacetophenone 、 2-amino-5-methyl-benzoic acid ethyl ester; thiocyanate 以 乙醇 为溶剂, 生成 7-methyl-5-oxo-1-phenyl-5H-thiazolo[3,2-a]quinazoline-2-carbonitrile
    参考文献:
    名称:
    Gakhar,H.K. et al., Journal of the Indian Chemical Society, 1971, vol. 48, p. 953 - 956
    摘要:
    DOI:
  • 作为产物:
    描述:
    苯甲酰乙腈 在 2,4,4,6-tetrabromo-3-n-pentadecylcyclohexa-2,5-dienone 作用下, 以 乙醚 为溶剂, 反应 10.0h, 以96%的产率得到1-bromo-1-cyanoacetophenone
    参考文献:
    名称:
    四溴氢化腰果酚:高效和可再生的溴化剂。
    摘要:
    2,4,4,6-四溴-3-正戊基-2,5-环己二酮(TBPCO)已被合成并用作新型高效,方便且环保的溴化剂。
    DOI:
    10.1021/ol061637b
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文献信息

  • NOVEL ORGANIC COMPOUND HAVING ELECTRON-TRANSPORTING AND/OR HOLE-BLOCKING PERFORMANCE AND ITS USE AND OLEDs COMPRISING THE COMPOUND
    申请人:WANG PengFei
    公开号:US20090102356A1
    公开(公告)日:2009-04-23
    Disclosed herein are several organic compounds having electron-transporting and/or hole-blocking performance and their preparation method and use and the OLEDs comprising the organic compound. The organic compounds exhibit high ionization potential (IP), electron affinity (Ea), glass transition temperature (Tg) and high electron mobility, and are a kind of good electron-transporting material with good hole-blocking ability. The devices comprising these compounds as one of the emitting layer, electron-transporting layer (ETL) and hole-blocking layer (HBL) show improved efficiency and better color purity.
    本文披露了几种具有电子传输和/或阻挡空穴性能的有机化合物,以及它们的制备方法和用途,以及包含该有机化合物的OLED。这些有机化合物具有高电离势(IP)、电子亲和力(Ea)、玻璃化转变温度(Tg)和高电子迁移率,并且是一种具有良好阻挡空穴能力的良好电子传输材料。包含这些化合物作为发射层、电子传输层(ETL)和阻挡空穴层(HBL)之一的器件显示出提高的效率和更好的色纯度。
  • [EN] PESTICIDAL COMPOSITIONS<br/>[FR] COMPOSITIONS PESTICIDES
    申请人:DOW AGROSCIENCES LLC
    公开号:WO2011017513A1
    公开(公告)日:2011-02-10
    The present invention concerns novel heteroaryl-N-aryl carbamates and their use in pest control, as insecticides and acaricides This invention also includes preparation of the pesticide compositions containing the compounds, and methods of controlling insects using the compounds.
    本发明涉及新型杂环基-N-芳基氨基甲酸酯及其在害虫控制中的应用,作为杀虫剂和杀螨剂。该发明还包括含有这些化合物的杀虫剂组合物的制备,以及利用这些化合物控制昆虫的方法。
  • [EN] 2-ACYLAMINOTHIAZOLE DERIVATIVES<br/>[FR] DERIVES DE 2-ACYLAMINOTHIAZOLE
    申请人:LUNDBECK & CO AS H
    公开号:WO2006032273A1
    公开(公告)日:2006-03-30
    The Invention relates to compounds of the formula I, wherein the variables are as defined in the claims, for use as a medicament. The compounds are A2A-receptor legends and are useful in the treatment of neurological and psychiatric disorders where an A2A-receptor is implicated.
    这项发明涉及到公式I的化合物,其中变量如索赔中定义的那样,用作药物。这些化合物是A2A受体的传奇,并在治疗神经系统和精神疾病方面发挥作用,其中A2A受体起到作用。
  • Benzimidazole derivatives and their use as KDR kinase protein inhibitors
    申请人:Babin Didier
    公开号:US20050009894A1
    公开(公告)日:2005-01-13
    The invention discloses and claims benzimidazole compounds of formula (I): wherein X is C—R2; Y is C—R2 or C—R3; W and Z are each C—R3; R1 is an optionally substituted aryl, heteroaryl or a saturated 5- or 6-membered monocyclic heterocyclic radical or a bicyclic heterocyclic radical; and A5 is H or alkyl; or a stereoisomer, a racemate, an enantiomer or a diastereoisomer of said compound of formula (I) or a pharmaceutically acceptable salt thereof; the use of compounds of formula (I) for the treatment of a disorder of proliferation of blood vessels, uncontrolled angiogenesis, a fibrotic disorder, a disorder of proliferation of mesangial cells, a metabolic disorder, allergy, asthma, thrombosis, a disease of the nervous system, retinopathy, psoriasis, rheumatoid arthritis, diabetes, muscle degeneration, solid tumors and cancers, pharmaceutical compositions comprising a compound of formula (I) and one or more pharmaceutically acceptable adjuvants or diluents and pharmaceutical compositions comprising a compound of formula (I) and one or more. antimitiotic agents.
    该发明公开和要求具有以下结构的苯并咪唑化合物(I):其中X为C—R2;Y为C—R2或C—R3;W和Z均为C—R3;R1为选择性取代的芳基、杂环芳基或饱和的5-或6-成员单环杂环基或双环杂环基;A5为H或烷基;或者为该化合物的立体异构体、拉克酸盐、对映异构体或二对映异构体;该化合物的用途为治疗血管增殖障碍、不受控制的血管生成、纤维化障碍、系膜细胞增殖障碍、代谢障碍、过敏、哮喘、血栓形成、神经系统疾病、视网膜病变、银屑病、类风湿性关节炎、糖尿病、肌肉退化、实体肿瘤和癌症的药物组合物包括化合物(I)和一个或多个药用辅料或稀释剂,以及包括化合物(I)和一个或多个抗有丝分裂剂的药物组合物。
  • 2-acylaminothiazole derivatives
    申请人:H. Lundbeck A/S
    公开号:US07910613B2
    公开(公告)日:2011-03-22
    The Invention relates to compounds of the formula I, wherein the variables are as defined in the claims, for use as a medicament. The compounds are A2A-receptor legends and are useful in the treatment of neurological and psychiatric disorders where an A2A-receptor is implicated.
    本发明涉及公式I的化合物,其中变量如权利要求所定义,用作药物。这些化合物是A2A受体配体,并且在治疗神经和精神障碍中具有用处,其中涉及A2A受体。
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