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

2,5-Dimethyl-4-isobutyloxazol | 1196-94-7

中文名称
——
中文别名
——
英文名称
2,5-Dimethyl-4-isobutyloxazol
英文别名
4-Isobutyl-2,5-dimethyl-1,3-oxazole;2,5-dimethyl-4-(2-methylpropyl)-1,3-oxazole
2,5-Dimethyl-4-isobutyloxazol化学式
CAS
1196-94-7
化学式
C9H15NO
mdl
——
分子量
153.224
InChiKey
CRHIVGNUDCQNJY-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):
    2.8
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    26
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2,5-Dimethyl-4-isobutyloxazol盐酸 作用下, 以 正己烷氯仿 为溶剂, 反应 28.0h, 生成 methyl erythro-3-acetamido-3-acetyl-2-hydroxy-5-methyl-2-phenylhexanoate
    参考文献:
    名称:
    Diastereoselective Photochemical Synthesis of α-Amino-β-hydroxyketones by Photocycloaddition of Carbonyl Compounds to 2,5-Dimethyl-4-isobutyloxazole
    摘要:
    The photocycloaddition of aldehydes and alpha-ketoesters to 2,5-dimethyl-4-isobutyloxazole leads to bicyclic oxetanes with high to moderate (exo) diastereoselectivity that can be easily ring-opened to give alpha-amino-beta-hydroxyketones.
    DOI:
    10.1007/s00706-006-0474-4
  • 作为产物:
    描述:
    DL-亮氨酸五氯化磷 作用下, 以 吡啶氯仿 为溶剂, 反应 10.0h, 生成 2,5-Dimethyl-4-isobutyloxazol
    参考文献:
    名称:
    Diastereoselective Photochemical Synthesis of α-Amino-β-hydroxyketones by Photocycloaddition of Carbonyl Compounds to 2,5-Dimethyl-4-isobutyloxazole
    摘要:
    The photocycloaddition of aldehydes and alpha-ketoesters to 2,5-dimethyl-4-isobutyloxazole leads to bicyclic oxetanes with high to moderate (exo) diastereoselectivity that can be easily ring-opened to give alpha-amino-beta-hydroxyketones.
    DOI:
    10.1007/s00706-006-0474-4
点击查看最新优质反应信息

文献信息

  • HERBICIDAL AND FUNGICIDAL 5-OXY-SUBSTITUTED 3-PHENYLISOXAZOLINE-5-CARBOXAMIDES AND 5-OXY-SUBSTITUTED 3-PHENYLISOXAZOLINE-5-THIOAMIDES
    申请人:BAYER CROPSCIENCE AG
    公开号:US20150245616A1
    公开(公告)日:2015-09-03
    Herbicidally and fungicidally active 5-oxy-substituted 3-phenylisoxazoline-5-carboxamides and 5-oxy-substituted 3-phenylisoxazoline-5-thioamides of the formula (I) are described. In this formula (I), X, X 2 to X 6 , R 1 to R 4 are radicals such as hydrogen, halogen and organic radicals such as substituted alkyl. A is a bond or a divalent unit. Y is a chalcogen.
    具有除草和杀菌活性的5-氧代取代的3-苯基异噁唑啉-5-羧酰胺和5-氧代取代的3-苯基异噁唑啉-5-酰胺的化合物如下式(I)所述。 在这个式子(I)中,X,X2至X6,R1至R4是氢、卤素和有机基团,如取代烷基等。A是一个键或二价基团。Y是族元素。
  • INDAZOLE DERIVATIVES
    申请人:Buchler Ingrid Price
    公开号:US20110028447A1
    公开(公告)日:2011-02-03
    This invention relates to compounds, pharmaceutical compositions and methods for the treatment of a condition mediated by CB1 receptor activity in a mammalian subject including a human, which comprises administering to a mammal in need of such treatment a therapeutically effective amount of the compound of formula (I) wherein R 1 , R 2 and R 3 are as defined in this specification.
    这项发明涉及化合物、药物组合物和治疗由CB1受体活性介导的哺乳动物主体(包括人类)疾病的方法,包括向需要这种治疗的哺乳动物中施用化合物的治疗有效剂量,其化合物的结构式为(I),其中R1、R2和R3如本说明书中所定义。
  • HERBICIDALLY AND FUNGICIDALLY ACTIVE 3-HETEROARYL-ISOXAZOLINE-5-CARBOXAMIDES AND 3-HETEROARYL-ISOXAZOLINE-5-THIOAMIDES
    申请人:BAYER CROPSCIENCE AG
    公开号:US20150223461A1
    公开(公告)日:2015-08-13
    Herbicidally and fungicidally active 3-heteroaryl-isoxazoline-5-carboxamides and 3-heteroaryl-isoxazoline-5-thioamides Herbicidally and fungicidally active 3-heteroarylisoxazoline-5-carboxamides and 3-heteroarylisoxazoline-5-thioamides of the formula (I) are described. In this formula (I), R represents radicals such as hydrogen, halogen and organic radicals such as substituted alkyl. A is a bond or a divalent unit. Y is a chalcogen.
    具有除草和杀菌活性的3-杂环芳基异噁唑啉-5-羧酰胺和3-杂环芳基异噁唑啉-5-酰胺被描述为具有除草和杀菌活性的化合物。在公式(I)中,R代表氢,卤素和有机基团,例如取代的烷基。 A是一个键或二价基团。 Y是族元素。
  • THE CONVERSION OF α-AMINO ACIDS TO OXAZOLES
    作者:RICHARD H. WILEY
    DOI:10.1021/jo01165a006
    日期:1947.1
  • Takahashi,T.; Hayami,M., Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan, 1960, vol. 80, p. 895 - 901
    作者:Takahashi,T.、Hayami,M.
    DOI:——
    日期:——
查看更多