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Bis(4-methyl-1,3-dioxetan-2-yl)methanamine

中文名称
——
中文别名
——
英文名称
Bis(4-methyl-1,3-dioxetan-2-yl)methanamine
英文别名
bis(4-methyl-1,3-dioxetan-2-yl)methanamine
Bis(4-methyl-1,3-dioxetan-2-yl)methanamine化学式
CAS
——
化学式
C7H13NO4
mdl
——
分子量
175.18
InChiKey
SYSSXVSXHJFERK-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):
    -0.3
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    62.9
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • SULFONIC ACID SALT COMPOUND OF 4-CARBAMOYL-5-HYDROXY-IMIDAZOLE DERIVATIVE
    申请人:Nobuo Kato
    公开号:US20100210855A1
    公开(公告)日:2010-08-19
    The object is to provide a stable SM-108 derivative, which is effective as a carcinostatic agent, particularly an SM-108 derivative having good storage stability. An SM-108 compound having good storage stability can be produced by producing an organic sulfonic acid salt compound of SM-108. Further, a crystalline SM-108 compound containing a trace amount of an organic carboxylic acid can be produced by using an aqueous solution of the organic sulfonic acid salt of SM-108, and by adding an alkali metal salt of an organic carboxylic acid to the aqueous solution to neutralize the aqueous solution and then causing the crystal precipitation in the solution.
    本发明旨在提供一种稳定的SM-108衍生物,其作为癌症静止剂具有良好的储存稳定性,特别是具有良好储存稳定性的SM-108衍生物。可以通过制备SM-108的有机磺酸盐化合物来生产具有良好储存稳定性的SM-108化合物。此外,可以使用SM-108的有机磺酸盐水溶液,并向水溶液中加入有机羧酸的碱金属盐以中和水溶液,然后在溶液中引起晶体沉淀,从而产生含有微量有机羧酸的晶体SM-108化合物。
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同类化合物

全氟-1,2-二氧杂环丁烷 4-羟基甲基-3,3,4-三甲基-1,2-二氧杂环丁烷 3,3,4,4-四甲基-1,2-二氧杂环丁烷 2,2'-环二氧-2,2'-联金刚烷 1,2-二氧杂环丁烷 3-tert-butoxymethyl-3,4,4-trimethyl-1,2-dioxetane vinylidene carbonate 1,2-Dioxetan-3-one 3-methyl-3-(1-butyl)-1,2-dioxetane 3-methyl-3-ethyl-1,2-dioxetane 3-methyl-3-(1-propyl)-1,2-dioxetane 3-methyl-1,2-dioxetane trans-3,4-dimethyl-1,2-dioxetane cis-3,4-dimethyl-1,2-dioxetane cis,trans-3,4-dimethyl-1,2-dioxetane tetraethyldioxetane tetramethyldioxetane 3,3-diethyl-1,2-dioxetane 3,3-dimethyl-4-ethyl-1,2-dioxetane 3-<<(chlorosulfonyl)carbamoyloxy>methyl>-3,4,4-trimethyl-1,2-dioxetane (3,4,4-Trimethyldioxetan-3-yl)methyl acetate spiro-cyclopentyl-1,2-dioxetanone 1,4,6-Tri-tert-butyl-2,3-dioxa-5-azabicyclo[2.2.0]hex-5-ene 3,3-Di(propan-2-yl)-1,2-dioxetane 1-(4,4-dimethyl-[1,2]dioxetan-3-yl)-ethanone 3-Butyl-3,4,4-trimethyl-1,2-dioxetane (3R,4S)-3,4-Dimethoxy-1,2-dioxetane N,N-Dimethylmethanamine--1,2-dioxetane (1/1) (3S,4S)-3,4-Dibutyl-[1,2]dioxetane (3S,4S)-3,4-Dipropyl-[1,2]dioxetane trans-3,4-diethyl-1,2-dioxetane 1,3-dioxetane 3,3-Dimethyl-1,2-dioxetan 3,3-pentamethylene-1,2-dioxetane tert.-Butyl-α-peroxylacton (3-Methyl-1,2-dioxa-spiro[3.5]non-3-yl)-methanol (3R,4S)-3,4-Dipropyl-[1,2]dioxetane (3R,4S)-3,4-Dibutyl-[1,2]dioxetane trimethyl-[1,2]dioxetane cis-3.4-diethyl-1.2-dioxetane tetra(methyl-d3)-1,2-dioxetane 3,3-dimethyl-4<2-methyl-1-propenyl>-1,2-dioxetane 3-methyl-3-(2-propyl)-1,2-dioxetane 3-methyl-3-tert-butyl-1,2-dioxetane 3-(ethoxymethyl)-3,4,4-trimethyl-1,2-dioxetane cyclohexene hydroperoxide (4S)-4-(1-hydroxy-2-methylpropan-2-yl)dioxetan-3-one (4R)-4-(1-hydroxy-2-methylpropan-2-yl)dioxetan-3-one [3-(Sulfanylmethyl)-2,4-dioxabicyclo[1.1.0]butan-1-yl]methanethiol (7S)-2,2-dimethyl-1,3-dioxaspiro[3.4]oct-5-en-7-ol