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5-Butyl-1,3-dimethylbarbituric acid | 7391-62-0

中文名称
——
中文别名
——
英文名称
5-Butyl-1,3-dimethylbarbituric acid
英文别名
5-butyl-1,3-dimethyl-barbituric acid;5-Butyl-1,3-dimethyl-barbitursaeure;5-butyl-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione;Barbituric acid, 5-butyl-1,3-dimethyl-;5-butyl-1,3-dimethyl-1,3-diazinane-2,4,6-trione
5-Butyl-1,3-dimethylbarbituric acid化学式
CAS
7391-62-0
化学式
C10H16N2O3
mdl
——
分子量
212.249
InChiKey
PAAOBODHLHVLMN-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):
    1.2
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    57.7
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:8b29e287026e60b32944460cb4343509
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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:
    叔丁基过氧化氢5-Butyl-1,3-dimethylbarbituric acidsodium nitrate溶剂黄146 作用下, 以 乙腈 为溶剂, 以58 %的产率得到5-butyl-5-(tert-butylperoxy)-1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione
    参考文献:
    名称:
    未分割电池中过氧自由基的电化学生成以及随后 1,3-二羰基的过氧化
    摘要:
    据报道,在恒定电流条件下,在完整的电化学电池中,氢过氧化物产生过氧自由基,随后选择性过氧化 1,3-二羰基。该方法提供了多种含过氧的巴比妥酸和4-羟基-2( 5H )-呋喃酮,收率高达74%。只有阳极和阴极过程的组合才能通过产生一组烷氧基和过氧自由基来提供有效的过氧化作用。 NaNO 3既充当电解质又充当自由基反应的氧化还原介体。
    DOI:
    10.1021/acs.orglett.3c03780
  • 作为产物:
    描述:
    参考文献:
    名称:
    巴比妥酸的单C-烷基化和单C-苄基化,通过锌/酸还原酰基,亚苄基和亚烷基巴比妥酸酯中间体
    摘要:
    通过系统地研究反应条件,开发了用于获得大量取代的5-烷基和5-苄基巴比妥酸的非常有效的制备方法。该过程包括两步准备,其中第二步是还原锌粉/酸。对于制备5-烷基巴比妥酸酯,第一步是制备5-酰基或5-亚烷基巴比妥酸酯。如果5-苄基巴比妥酸酯是目标产物,则第一步包括制备5-亚苄基。无论第一步的性质如何,所有反应的合成产率均约为90%,而分离和纯化仅涉及结晶。
    DOI:
    10.1016/s0040-4039(03)00111-4
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文献信息

  • POLARIZING PLATE PROTECTIVE FILM, POLARIZING PLATE, AND DISPLAY DEVICE
    申请人:FUJIFILM Corporation
    公开号:US20170226317A1
    公开(公告)日:2017-08-10
    A polarizing plate protective film which prevents deterioration of polarization performance in a high temperature, high humidity environment, and a polarizing plate and display device using the film including a compound represented by the following General Formula (I). (X-L n z General Formula (I) X represents a formyl group, a boronic acid group, or a group represented by the following General Formula (I-B) or a group represented by the following General Formula (I-C), where L represents a single bond or divalent linking group, and n represents an integer equal to or greater than 2. When n is 2, Z represents a single bond or a divalent group, and when n≧3, Z represents an n-valent group. R A and R B represent an alkyl group, a cycloalkyl group, an aryl group, or an acyl group. R A and R B may be bonded to each other to form a ring. * represents a bond to be bonded to L.
    一种偏光板保护膜,可防止在高温高湿环境中偏光性能的恶化,以及使用包括下述一般式(I)所代表的化合物的偏光板和显示装置。 (X-L n z 一般式(I) X代表甲酰基、硼酸基或由下述一般式(I-B)所代表的基团或由下述一般式(I-C)所代表的基团,其中L代表单键或二价连接基团,n代表大于或等于2的整数。当n为2时,Z代表单键或二价基团,当n≧3时,Z代表n价基团。 RA和RB代表烷基、环烷基、芳基或酰基。RA和RB可以相互连接形成环。*代表要连接到L的键。
  • Kharasch reaction: Cu-catalyzed and non-Kharasch metal-free peroxidation of barbituric acids
    作者:Oleg V. Bityukov、Vera A. Vil'、George K. Sazonov、Andrey S. Kirillov、Nikita V. Lukashin、Gennady I. Nikishin、Alexander O. Terent'ev
    DOI:10.1016/j.tetlet.2019.02.042
    日期:2019.3
    It was discovered that the Kharasch peroxidation of barbituric acids proceeds both with a Cu-catalyst and without a metal catalyst. Despite the presence of possible thermal-initiated side oxidation pathways, α-tert-butylperoxybarbiturates were selectively prepared from substituted barbituric acids and tert-butyl hydroperoxide.
    已发现巴比妥酸的Kharasch过氧化在有铜催化剂和没有金属催化剂的情况下都进行。尽管可能热引发侧氧化途径的存在下,α-叔-butylperoxybarbiturates被选择性地从取代的巴比土酸和制备叔丁基过氧化氢。
  • DENTAL CEMENT
    申请人:KURARAY NORITAKE DENTAL INC.
    公开号:US20170135909A1
    公开(公告)日:2017-05-18
    The present invention provides a dental cement that exhibits excellent adhesiveness to dentin and has high mechanical strength. The present invention relates to a multi-part dental cement containing: an asymmetric acrylamide-methacrylic acid ester compound (a); an acid group-containing (meth)acrylic polymerizable monomer (b); a hydrophobic crosslinkable polymerizable monomer (c); a chemical polymerization initiator (d); and a filler (e). The asymmetric acrylamide-methacrylic acid ester compound (a) is represented by the following general formula (1): where X is an optionally substituted, linear or branched C 1 to C 6 aliphatic group or an optionally substituted aromatic group, the aliphatic group is optionally interrupted by at least one linking group selected from the group consisting of —O—, —S—, —CO—, —CO—O—, —O—CO—, —NR 1 —, —CO—NR 1 —, —NR 1 —CO—, —CO—O—NR 1 —, —O—CO—NR 1 —, and —NR 1 —CO—NR 1 —, and R 1 is a hydrogen atom or an optionally substituted, linear or branched C 1 to C 6 aliphatic group.
    本发明提供一种对牙本质具有良好粘附性并具有高机械强度的牙科水泥。本发明涉及一种含有多部分的牙科水泥,包括:一种不对称的丙烯酰胺-甲基丙烯酸酯化合物(a);一种含酸基的(甲基)丙烯酸聚合单体(b);一种疏水性交联聚合单体(c);一种化学聚合引发剂(d);和一种填料(e)。不对称的丙烯酰胺-甲基丙烯酸酯化合物(a)由以下一般式(1)表示:其中X是可选择取代的线性或支链的C1到C6脂肪族基团或可选择取代的芳香族基团,脂肪族基团可选择地被来自由—O—、—S—、—CO—、—CO—O—、—O—CO—、—NR1—、—CO—NR1—、—NR1—CO—、—CO—O—NR1—、—O—CO—NR1—和—NR1—CO—NR1—组成的至少一种连接基团中断,且R1是氢原子或可选择取代的线性或支链的C1到C6脂肪族基团。
  • DENTAL ADHESIVE
    申请人:KURARAY NORITAKE DENTAL INC.
    公开号:US20170196778A1
    公开(公告)日:2017-07-13
    The present invention provides a dental adhesive exhibiting excellent initial bond strength and bond durability to both enamel and dentin. The present invention relates to a dental adhesive containing: an asymmetric acrylamide-methacrylic acid ester compound (a); an acid group-containing (meth)acrylic polymerizable monomer (b); and a water-soluble polymerizable monomer (c). The asymmetric acrylamide-methacrylic acid ester compound (a) is represented by the following general formula (1): where X is an optionally substituted, linear or branched C 1 to C 6 aliphatic group or an optionally substituted aromatic group, the aliphatic group is optionally interrupted by at least one linking group selected from the group consisting of —O—, —S—, —CO—, —CO—O—, —O—CO—, —NR 1 —, —CO—NR 1 —, —NR 1 —CO—, —CO—O—NR 1 —, —O—CO—NR 1 —, and —NR 1 —CO—NR 1 —, and R 1 is a hydrogen atom or an optionally substituted, linear or branched C 1 to C 6 aliphatic group.
    本发明提供了一种牙科粘接剂,具有优异的初始粘接强度和对牙釉质和牙本质的粘接耐久性。本发明涉及一种含有以下成分的牙科粘接剂:不对称丙烯酰胺-甲基丙烯酸酯化合物(a);含酸基的(甲基)丙烯酸聚合单体(b);以及水溶性聚合单体(c)。不对称丙烯酰胺-甲基丙烯酸酯化合物(a)由下述一般式(1)表示:其中X是可选择取代的线性或支链状的C1到C6脂肪族基或可选择取代的芳香族基,所述脂肪族基可被来自由—O—、—S—、—CO—、—CO—O—、—O—CO—、—NR1—、—CO—NR1—、—NR1—CO—、—CO—O—NR1—、—O—CO—NR1—和—NR1—CO—NR1—组成的至少一个连接基中断,R1为氢原子或可选择取代的线性或支链状的C1到C6脂肪族基。
  • MULTI-PART DENTAL CEMENT
    申请人:KURARAY NORITAKE DENTAL INC.
    公开号:US20190262240A1
    公开(公告)日:2019-08-29
    The present invention provides a dental cement showing excellent storage stability, undergoing little change in paste properties during long-term storage, and having a small solidification risk during long-term storage. The present invention relates to a multi-part dental cement comprising: a first paste comprising an acid group-containing (meth)acrylic polymerizable monomer (a), a polyfunctional (meth)acrylic polymerizable monomer (b) containing no acid group, an oxidizing agent (c-1) of a chemical polymerization initiator, and a filler (d); and a second paste comprising a polyfunctional (meth)acrylic polymerizable monomer (b) containing no acid group, a reducing agent (c-2) of a chemical polymerization initiator, and a filler (e), wherein the filler (d) is treated with a surface treatment agent and has an average particle diameter of 0.01 to 50.0 μm, the surface treatment agent comprises a silane coupling agent (A) represented by the general formula (1) and an organosilazane (B) represented by the general formula (2).
    本发明提供了一种牙科水泥,具有出色的储存稳定性,在长期储存期间,其糊剂性能变化很小,并且在长期储存期间固化风险较小。本发明涉及一种多部分牙科水泥,包括:第一糊剂,包括含有酸基的(甲基)丙烯酸聚合单体(a),不含酸基的多官能团(甲基)丙烯酸聚合单体(b),化学聚合引发剂的氧化剂(c-1),和填料(d);以及第二糊剂,包括不含酸基的多官能团(甲基)丙烯酸聚合单体(b),化学聚合引发剂的还原剂(c-2),和填料(e),其中填料(d)经过表面处理剂处理,平均粒径为0.01至50.0μm,表面处理剂包括通式(1)表示的硅烷偶联剂(A)和通式(2)表示的有机硅氮烷(B)。
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