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(2SR)-(3SR)-3-nitro-1,1,1-trifluoro-2-heptanol

中文名称
——
中文别名
——
英文名称
(2SR)-(3SR)-3-nitro-1,1,1-trifluoro-2-heptanol
英文别名
1,1,1-trifluoro-3-nitroheptan-2-ol
(2SR)-(3SR)-3-nitro-1,1,1-trifluoro-2-heptanol化学式
CAS
——
化学式
C7H12F3NO3
mdl
——
分子量
215.172
InChiKey
YEDAKNYXPPTQRJ-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):
    2.3
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    66
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    1-硝基戊烷1-乙氧基-2,2,2-三氟乙醇potassium carbonate盐酸氯化钠magnesium sulfate 作用下, 以 乙酸乙酯 为溶剂, 反应 3.0h, 以to give (2SR)-(3SR)-3-nitro-1,1,1-trifluoro-2-heptanol as a crude oil (1.7 g, 93%)的产率得到(2SR)-(3SR)-3-nitro-1,1,1-trifluoro-2-heptanol
    参考文献:
    名称:
    Peptide and peptide analog protease inhibitors
    摘要:
    提供了用于治疗以淀粉样物质沉积为特征的疾病的化合物和复合物的使用方法。这些化合物包括公式I和II中的化合物:## STR1 ## 其中R.sub.1最好是2-甲基丙烯、2-丁烯、环己基或环己基甲基;R.sub.2、R.sub.4和R.sub.8各自独立地是甲基或乙基;R.sub.3最好是异丁基或苯基;R.sub.5最好是异丁基;R.sub.6是氢或甲基;R.sub.7--(Q).sub.n最好是苄氧羰基或乙酰基;Q最好是--C(O)-;R.sub.B最好是异丁基;--R.sub.A =--(T).sub.m--(D).sub.m--R.sub.1,其中T最好是氧或碳,D最好是一种单不饱和的C.sub.3-4烯基,更好的是;X最好是α-酮酸酯或α-酮酰胺或醛。
    公开号:
    US06015879A1
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文献信息

  • Peptide and peptide analog protease inhibitors
    申请人:SIBIA Neurosciences, Inc.
    公开号:US05714471A1
    公开(公告)日:1998-02-03
    Methods of use of compounds and compounds for the treatment of disorders characterized by the cerebral deposition of amyloid are provided. Among the compounds are those of formulae I and II: ##STR1## in which R.sub.1 is preferably 2-methyl propene, 2-butene, cyclohexyl or cyclohexylmethyl; R.sub.2, R.sub.4, and R.sub.8 are each independently methyl or ethyl; R.sub.3 is preferably iso-butyl or phenyl; R.sub.5 is preferably iso-butyl; R.sub.6 is H or methyl; R.sub.7 --(Q).sub.n is preferably benzyloxycarbonyl or acetyl; Q is preferably --C(O)--; R.sub.8 is preferbly iso-butyl; R.sub.A =--(T).sub.m --(D).sub.m --R.sub.1, is which T is preferably oxygen or carbon, and D is preferably a mono-unsaturated C.sub.3-4 alkenyl being more preferred; and X is preferably an .alpha.-ketoester or .alpha.-ketoamide.
    提供了用于治疗以淀粉样物质沉积为特征的疾病的化合物的使用方法和化合物。其中化合物包括式I和式II:##STR1## 其中R.sub.1优选为2-甲基丙烯,2-丁烯,环己基或环己基甲基;R.sub.2,R.sub.4和R.sub.8各自独立地为甲基或乙基;R.sub.3优选为异丁基或苯基;R.sub.5优选为异丁基;R.sub.6为H或甲基;R.sub.7--(Q).sub.n优选为苄氧羰基或乙酰基;Q优选为--C(O)--;R.sub.8优选为异丁基;R.sub.A=--(T).sub.m--(D).sub.m--R.sub.1,其中T优选为氧或碳,D优选为一种单不饱和的C.sub.3-4烯烃,更优选;X优选为α-酮酸酯或α-酮酰胺。
  • Methods of treating neurodegenerative disorders using protease inhibitors
    申请人:SIBIA Neurosciences Inc.
    公开号:US06051684A1
    公开(公告)日:2000-04-18
    Methods of use of compounds for the treatment of disorders characterized by the cerebral deposition of amyloid are provided. Among the compounds provided for use in the methods are those of the formula: ##STR1## in which R.sub.1 is preferably 2-methylpropenyl, 2-butenyl, cyclohexyl or cyclohexylmethyl; R.sub.2, R.sub.4, and R.sub.8 are each preferably independently methyl or ethyl; R.sub.3 is preferably iso-butyl or phenyl; R.sub.5 is preferably iso-butyl; R.sub.6 is preferably H or methyl; R.sub.7 --(Q).sub.n is preferably benzyloxycarbonyl or acetyl; Q is preferably --C(O)--; and X is preferably an aldehyde, .alpha.-ketoester or .alpha.-ketoamide.
    提供了用于治疗由淀粉样物质脑沉积所表征的疾病的化合物使用方法。提供的化合物中,用于该方法的化合物包括以下结构式:##STR1##在该结构式中,R.sub.1最好是2-甲基丙烯基、2-丁烯基、环己基或环己基甲基;R.sub.2、R.sub.4和R.sub.8最好分别独立地是甲基或乙基;R.sub.3最好是异丁基或苯基;R.sub.5最好是异丁基;R.sub.6最好是H或甲基;R.sub.7--(Q).sub.n最好是苄氧羰基或乙酰基;Q最好是--C(O)--;X最好是醛、α-酮酸酯或α-酮酰胺。
  • Peptide, peptide analog and amino acid analog protease inhibitors
    申请人:Sibia Neurosciences, Inc.
    公开号:US06017887A1
    公开(公告)日:2000-01-25
    Methods of use of compounds and compounds for the treatment of disorders characterized by the cerebral deposition of amyloid are provided. Among the compounds are those of formulae (I), (II) and (III): ##STR1## in which R.sub.1 is preferably 2-methyl propene, 2-butene, norleucine; R.sub.2, R.sub.4, and R.sub.8 are each independently methyl or ethyl; R.sub.3 is preferably iso-butyl or phenyl; R.sub.5 is preferably iso-butyl; R.sub.6 is H or methyl; R.sub.7 --(Q).sub.n is preferably benzyloxycarbonyl or acetyl; Q is preferably --C(O)--; R.sub.B is preferbly iso-butyl; R.sub.A =--(T).sub.m --(D).sub.m --R.sub.1, is which T is preferably oxygen or carbon, and D is preferably a mono-unsaturated C.sub.3-4 alkenyl being more preferred; and X is an alcohol, particularly a secondary alcohol.
    提供了用于治疗以淀粉样物质脑沉积为特征的疾病的化合物和化合物使用的方法。其中化合物包括式(I),(II)和(III):##STR1## 在该式中,R.sub.1 最好是2-甲基丙烯,2-丁烯,正癸氨酸;R.sub.2、R.sub.4 和R.sub.8 各自独立地是甲基或乙基;R.sub.3 最好是异丁基或苯基;R.sub.5 最好是异丁基;R.sub.6 是H或甲基;R.sub.7--(Q).sub.n 最好是苄氧羰基或乙酰基;Q 最好是--C(O)-;R.sub.B 最好是异丁基;R.sub.A =--(T).sub.m--(D).sub.m--R.sub.1,在该式中,T 最好是氧或碳,D 最好是一种单不饱和的 C.sub.3-4 烯基,更好的是;X 是一种醇,特别是二级醇。
  • Methods for identifying compounds effective for treating
    申请人:SIBIA Neurosciences, Inc.
    公开号:US06153171A1
    公开(公告)日:2000-11-28
    Methods for identifying compounds that can be used for treatment of neurodegenerative diseases, for monitoring the progression of these diseases, and for monitoring therapeutic intervention of these diseases are provided. These methods are effected by determining the relative amount of .alpha.-sAPP and the ratio of .alpha.-sAPP to total sAPP in body fluids, tissues or in cell culture.
    提供了一种用于鉴定可用于治疗神经退行性疾病、监测这些疾病进展以及监测这些疾病治疗干预的化合物的方法。这些方法通过测定体液、组织或细胞培养中.alpha.-sAPP的相对量和.alpha.-sAPP与总sAPP的比值来实现。
  • US5714471A
    申请人:——
    公开号:US5714471A
    公开(公告)日:1998-02-03
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