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1,2-isopropylideneglyceraldehyde oxime | 756477-96-0

中文名称
——
中文别名
——
英文名称
1,2-isopropylideneglyceraldehyde oxime
英文别名
(R)-2,3-O-isopropylideneglyceraldehydeoxime;(E,Z)-(R)-2,3-O-isopropylidene-glyceraldoxime;(R)-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde oxime;N-[[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]methylidene]hydroxylamine
1,2-isopropylideneglyceraldehyde oxime化学式
CAS
756477-96-0
化学式
C6H11NO3
mdl
——
分子量
145.158
InChiKey
UBTBDPDJMQPNBM-RXMQYKEDSA-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):
    0.2
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    51
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1,2-isopropylideneglyceraldehyde oxime 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 反应 5.0h, 生成 2,2-二甲基-1,3-二氧戊环-4-甲胺
    参考文献:
    名称:
    (R)-和(S)-5-羟甲基-2-恶唑烷酮及其衍生物的有效途径
    摘要:
    2-恶唑烷酮由于其各种药理作用而成为一类非常有趣的化合物。从D-甘露醇,L-抗坏血酸和(R)-或(S)-苹果酸开始,已开发出两个对映体纯的(R)-和(S)-5-羟甲基-2-恶唑烷酮的新合成方法。(R)-和(S)-5-羟甲基-2-恶唑烷酮已用于合成一些新的手性2-恶唑烷酮衍生物。
    DOI:
    10.1016/0957-4166(95)00144-e
  • 作为产物:
    描述:
    5,6-O-isopropylidene-L-ascorbic acidsodium periodate 、 lithium aluminium tetrahydride 、 盐酸羟胺三乙胺 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 9.0h, 生成 1,2-isopropylideneglyceraldehyde oxime
    参考文献:
    名称:
    (R)-和(S)-5-羟甲基-2-恶唑烷酮及其衍生物的有效途径
    摘要:
    2-恶唑烷酮由于其各种药理作用而成为一类非常有趣的化合物。从D-甘露醇,L-抗坏血酸和(R)-或(S)-苹果酸开始,已开发出两个对映体纯的(R)-和(S)-5-羟甲基-2-恶唑烷酮的新合成方法。(R)-和(S)-5-羟甲基-2-恶唑烷酮已用于合成一些新的手性2-恶唑烷酮衍生物。
    DOI:
    10.1016/0957-4166(95)00144-e
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文献信息

  • A Simple System for Preparation of Protected Glycosidic Carbohydrate Nitriles from Corresponding Oximes
    作者:Vikas N. Telvekar、Krishnacharya G. Akamanchi
    DOI:10.1081/scc-120039485
    日期:2004.1.1
    Abstract Glycosidic nitriles of protected carbohydrates were prepared efficiently and rapidly from the corresponding oximes using thionyl chloride/benzotriazole combination as dehydrating system.
    摘要 以亚硫酰氯/苯并三唑组合为脱水体系,以相应的肟为原料,高效、快速地制备了受保护碳水化合物的糖苷腈。
  • Pyridin-2-YL-Amino-1, 2, 4-Thiadiazole Derivatives as Glucokinase Activators for the Treatment of Diabetes Mellitus
    申请人:Aicher Thomas Daniel
    公开号:US20100204240A1
    公开(公告)日:2010-08-12
    Provided are compounds of Formula (I): wherein R 2 , R 3 , R 13 , L and D 2 are as defined in the specification, which are useful in the treatment and/or prevention of diseases or disorders mediated by deficient levels of glucokinase activity or which can be treated by activating glucokinase including, but not limited to, diabetes mellitus, impaired glucose tolerance, IFG (impaired fasting glucose) and IFG (impaired fasting glycemia), as well as other diseases and disorders such as those discussed herein.
    提供的化合物式(I)如下:其中R2、R3、R13、L和D2如规范中所定义,这些化合物可用于治疗和/或预防由于葡萄糖激酶活性不足引起或可以通过激活葡萄糖激酶治疗的疾病或紊乱,包括但不限于糖尿病、糖耐量受损、IFG(空腹血糖受损)和IFG(空腹高血糖),以及本文所讨论的其他疾病和紊乱。
  • Pyridin-2YL-Amino-1, 2, 4-Thiadiazole Derivatives as Glucokinase Activators for the Treatment of Diabetes Mellitus
    申请人:AICHER Thomas Daniel
    公开号:US20120277242A1
    公开(公告)日:2012-11-01
    Provided are compounds of Formula (I): wherein R 2 , R 3 , R 13 , L and D 2 are as defined in the specification, which are useful in the treatment and/or prevention of diseases or disorders mediated by deficient levels of glucokinase activity or which can be treated by activating glucokinase including, but not limited to, diabetes mellitus, impaired glucose tolerance, IFG (impaired fasting glucose) and IFG (impaired fasting glycemia), as well as other diseases and disorders such as those discussed herein.
    本发明提供了式(I)的化合物:其中R2、R3、R13、L和D2如规范中所定义,它们在治疗和/或预防由葡萄糖激酶活性不足介导的疾病或疾病中有用,或者可以通过激活葡萄糖激酶来治疗,包括但不限于糖尿病、糖耐量受损、IFG(空腹血糖受损)和IFG(空腹高血糖),以及其他疾病和疾病,如在此处所讨论的。
  • Pyridin-2-yl-amino-1, 2, 4-thiadiazole derivatives as glucokinase activators for the treatment of diabetes mellitus
    申请人:Array BioPharma, Inc.
    公开号:US08212045B2
    公开(公告)日:2012-07-03
    Provided are compounds of Formula (I): wherein R2, R3, R13, L and D2 are as defined in the specification, which are useful in the treatment and/or prevention of diseases or disorders mediated by deficient levels of glucokinase activity or which can be treated by activating glucokinase including, but not limited to, diabetes mellitus, impaired glucose tolerance, IFG (impaired fasting glucose) and IFG (impaired fasting glycemia), as well as other diseases and disorders such as those discussed herein.
    提供的化合物式(I)如下:其中R2、R3、R13、L和D2如规范中所定义,可用于治疗和/或预防由于葡萄糖激酶活性不足而介导的疾病或疾病,或可通过激活葡萄糖激酶来治疗,包括但不限于糖尿病、糖耐量受损、空腹血糖受损(IFG)和空腹高血糖(IFG),以及其他在此处讨论的疾病和紊乱。
  • Pyridin-2yl-amino-1, 2, 4-thiadiazole derivatives as glucokinase activators for the treatment of diabetes mellitus
    申请人:Aicher Thomas Daniel
    公开号:US08853409B2
    公开(公告)日:2014-10-07
    Provided are compounds of Formula (I): wherein R2, R3, R13, L and D2 are as defined in the specification, which are useful in the treatment and/or prevention of diseases or disorders mediated by deficient levels of glucokinase activity or which can be treated by activating glucokinase including, but not limited to, diabetes mellitus, impaired glucose tolerance, IFG (impaired fasting glucose) and IFG (impaired fasting glycemia), as well as other diseases and disorders such as those discussed herein.
    提供的是公式(I)化合物:其中R2,R3,R13,L和D2如规范中所定义,这些化合物对于治疗和/或预防由葡萄糖激酶活性不足引起或可以通过激活葡萄糖激酶来治疗的疾病或疾病具有用处,包括但不限于糖尿病,糖耐量受损,IFG(空腹血糖受损)和IFG(空腹高血糖),以及其他疾病和疾病,如本文所述。
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