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2,6-二甲基-4-嘧啶甲醛 | 1074-39-1

中文名称
2,6-二甲基-4-嘧啶甲醛
中文别名
2,6-二甲基嘧啶-4-甲醛
英文名称
2,6-dimethyl-pyrimidine-4-carbaldehyde
英文别名
2,6-Dimethyl-pyrimidin-4-carbaldehyd;2,6-Dimethylpyrimidine-4-carbaldehyde
2,6-二甲基-4-嘧啶甲醛化学式
CAS
1074-39-1
化学式
C7H8N2O
mdl
——
分子量
136.153
InChiKey
DDNZMSHBGPIXPX-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:
    233.6±20.0 °C(Predicted)
  • 密度:
    1.133±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.5
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    42.8
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933599090

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

  • 作为产物:
    描述:
    2,6-dimethyl-4(E)-styrylpyrimidine 在 氯仿氧气臭氧 作用下, 生成 2,6-二甲基-4-嘧啶甲醛
    参考文献:
    名称:
    Ochiai; Yanai, Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan, 1938, vol. 58, p. 397,399; dtsch. Ref. S. 76, 77
    摘要:
    DOI:
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文献信息

  • OPTICAL RECORDING MEDIUM AND AZO METAL CHELATE COMPOUND
    申请人:Mitsui Chemicals, Inc.
    公开号:EP1997856A1
    公开(公告)日:2008-12-03
    The present invention is to provide an optical recording medium which is capable of performing good recording and reproducing by using a laser having a wavelength of 300 to 900 nm, a novel azo metal chelate compound, and a novel azo compound. Furthermore, the present invention is to provide an optical recording medium having an azo metal chelate compound in a recording layer.
    本发明提供了一种光记录介质,通过使用波长为300至900纳米的激光、一种新型偶氮金属螯合物和一种新型偶氮化合物,能够进行良好的记录和再现。此外,本发明提供了一种在记录层中含有偶氮金属螯合物的光记录介质。
  • Substituted indolizine-like compounds and methods of use
    申请人:——
    公开号:US20030195221A1
    公开(公告)日:2003-10-16
    Selected novel substituted indolizine-like compounds are effective for treatment of diseases, such as TNF-&agr;, IL-1&bgr;, IL-6 and/or IL-8 mediated diseases, and other maladies, such as cancer, pain and diabetes. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for treatment of diseases and other maladies or conditions involving inflammation, cancer, pain, diabetes and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    选定的类似吲哚啉的化合物对治疗疾病,如TNF-α、IL-1β、IL-6和/或IL-8介导的疾病,以及其他疾病,如癌症、疼痛和糖尿病具有有效性。本发明涵盖了新型化合物、类似物、前药和其药用可接受盐、制药组合物以及治疗涉及炎症、癌症、疼痛、糖尿病等疾病和其他疾患或情况的方法。该发明还涉及制备此类化合物的方法,以及在此类过程中有用的中间体。
  • Substituted heterocyclic compounds and methods of use
    申请人:Liu Longbin
    公开号:US20050043301A1
    公开(公告)日:2005-02-24
    The present invention relates to compounds having the general formula or a pharmaceutically acceptable salt thereof, wherein R 1 is a saturated or unsaturated 5-, 6- or 7-membered, ring containing 0, 1, 2 or 3 atoms selected from N, O and S, wherein the ring may be fused with a benzo group, and is substituted by 0, 1 or 2 oxo groups, and wherein R 1 is additionally substituted; and R 2 is a substituted C 1-6 alkyl. Also included is a method of prophylaxis or treatment of inflammation, rheumatoid arthritis, Pagets disease, osteoporosis, multiple myeloma, uveititis, acute or chronic myelogenous leukemia, pancreatic β cell destruction, osteoarthritis, rheumatoid spondylitis, gouty arthritis, inflammatory bowel disease, adult respiratory distress syndrome (ARDS), psoriasis, Crohn's disease, allergic rhinitis, ulcerative colitis, anaphylaxis, contact dermatitis, asthma, muscle degeneration, cachexia, Reiter's syndrome, type I diabetes, type II diabetes, bone resorption diseases, graft vs. host reaction, Alzheimer's disease, stroke, myocardial infarction, ischemia reperfusion injury, atherosclerosis, brain trauma, multiple sclerosis, cerebral malaria, sepsis, septic shock, toxic shock syndrome, fever, myalgias due to HIV-1, HIV-2, HIV-3, cytomegalovirus (CMV), influenza, adenovirus, the herpes viruses or herpes zoster infection in a mammal comprising administering an effective amount a compound as described above.
    本发明涉及具有一般式的化合物或其药学上可接受的盐,其中R1是饱和或不饱和的5、6或7成员环,含有0、1、2或3个来自N、O和S的原子,其中环可能与苯环融合,并且被0、1或2个氧代基取代,并且R1还被取代;R2是取代的C1-6烷基。还包括一种预防或治疗炎症、类风湿性关节炎、帕盖特病、骨质疏松症、多发性骨髓瘤、葡萄膜炎、急性或慢性骨髓性白血病、胰岛素β细胞破坏、骨关节炎、类风湿脊柱炎、痛风性关节炎、炎症性肠病、成人呼吸窘迫综合征(ARDS)、牛皮癣、克罗恩病、过敏性鼻炎、溃疡性结肠炎、过敏性休克、接触性皮炎、哮喘、肌肉退化、消瘦症、Reiter综合征、I型糖尿病、II型糖尿病、骨吸收疾病、移植物抗宿主反应、阿尔茨海默病、中风、心肌梗死、缺血再灌注损伤、动脉粥样硬化、脑外伤、多发性硬化症、脑型疟疾、败血症、感染性休克、毒性休克综合征、发热、HIV-1、HIV-2、HIV-3、巨细胞病毒(CMV)、流感、腺病毒、单纯疱疹病毒或带状疱疹感染引起的肌肉疼痛的方法,包括向哺乳动物施用上述化合物的有效量。
  • Substituted pyrimidine compounds and methods of use
    申请人:Amgen Inc.
    公开号:US20030069425A1
    公开(公告)日:2003-04-10
    Selected novel substituted pyrimidine compounds are effective for prophylaxis and treatment of diseases, such as TNF-&agr;, IL-1&bgr;, IL-6 and/or IL-8 mediated diseases, and other maladies, such as pain and diabetes. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving inflammation, pain, diabetes and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    选择的新型代替嘧啶类化合物可用于预防和治疗诸如TNF-α、IL-1β、IL-6和/或IL-8介导的疾病,以及其他疾病,如疼痛和糖尿病。该发明涵盖了新型化合物、类似物、前药及其药学上可接受的盐、制药组合物和用于预防和治疗涉及炎症、疼痛、糖尿病等疾病和其他疾病或病况的方法。该发明还涉及制备这种化合物的过程,以及在这些过程中有用的中间体。
  • Substituted pyridone compounds and methods of use
    申请人:Amgen Inc.
    公开号:US20030073704A1
    公开(公告)日:2003-04-17
    Selected novel substituted pyrimidinone and pyridone compounds are effective for prophylaxis and treatment of diseases, such as TNF-&agr;, IL-1&bgr;, IL-6 and/or IL-8 mediated diseases, and other maladies, such as pain and diabetes. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving inflammation, pain, diabetes and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.
    选定的新型嘧啶酮和吡啶酮化合物对于预防和治疗疾病(如TNF-α、IL-1β、IL-6和/或IL-8介导的疾病)以及其他疾病(如疼痛和糖尿病)是有效的。该发明涵盖了新型化合物、类似物、前药和其药学上可接受的盐、制药组合物以及用于预防和治疗涉及炎症、疼痛、糖尿病等疾病和其他疾患或病况的方法。该发明还涉及制造这些化合物的过程以及在这些过程中有用的中间体。
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