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methyl 3,4,6-tri-O-methylglucopyranoside | 3149-56-2

中文名称
——
中文别名
——
英文名称
methyl 3,4,6-tri-O-methylglucopyranoside
英文别名
methyl 3,4,6-tri-O-methyl-D-glucopyranoside;(3R,4R,5R,6R)-2,4,5-trimethoxy-6-(methoxymethyl)oxan-3-ol
methyl 3,4,6-tri-O-methylglucopyranoside化学式
CAS
3149-56-2
化学式
C10H20O6
mdl
——
分子量
236.265
InChiKey
MJCQVUQCEVACLB-WWGUJXLXSA-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

物化性质

  • 沸点:
    329.9±42.0 °C(Predicted)
  • 密度:
    1.14±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1
  • 重原子数:
    16
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    66.4
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    eruberin A盐酸 、 sodium hydride 作用下, 反应 7.5h, 生成 methyl 3,4,6-tri-O-methylglucopyranoside
    参考文献:
    名称:
    Tanaka, Nobutoshi; Sada, Takuro; Murakami, Takao, Chemical and pharmaceutical bulletin, 1984, vol. 32, # 2, p. 490 - 496
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Apioglycyrrhizin and araboglycyrrhizin, two new sweet oleanene-type triterpene oligoglycosides from the root of Glycyrrhiza inflata.
    作者:Isao KITAGAWA、Masahiro SAKAGAMI、Fumi HASHIUCHI、Jun Liang ZHOU、Masayuki YOSHIKAWA、Jiali REN
    DOI:10.1248/cpb.37.551
    日期:——
    Two new sweet oleanene-type triterpene oligoglycosides, named apioglycyrrhizin and araboglycyrrhizin, were isolated from the air-drie root of Glycyrrhiza inflata [Chinese Glycyrrhizae Radix, Shinkyo-kanzo in Japanese], and their structures have been determined on the basis of chemical and physicochemical evidence.
    从胀果甘草(中药名为甘草,日文名为新娇甘)的干燥根中分离出两种新的甘遂型三萜寡糖苷,分别命名为芹菜苷甘草酸和阿拉伯苷甘草酸,并通过化学和物理化学证据确定了它们的结构。
  • Structural analysis of novel kestose isomers isolated from sugar beet molasses
    作者:Norio Shiomi、Tatsuya Abe、Hiroto Kikuchi、Tsutomu Aritsuka、Yusuke Takata、Eri Fukushi、Yukiharu Fukushi、Jun Kawabata、Keiji Ueno、Shuichi Onodera
    DOI:10.1016/j.carres.2016.02.002
    日期:2016.4
    GC-FID and GC-MS analyses of methyl derivatives, MALD-TOF-MS measurements and NMR spectra were used to confirm the structural characteristics of the isomers. The (1)H and (13)C NMR signals of each isomer saccharide were assigned using COSY, E-HSQC, HSQC-TOCSY, HMBC and H2BC techniques. These kestose isomers were identified as α-D-fructofuranosyl-(2- > 2)-α-D-glucopyranosyl-(1 < ->2)-β-D-fructofuranoside
    通过碳-塞利特柱色谱法和HPLC从甜菜糖蜜中分离出八种KestOSe异构体。甲基衍生物的GC-FID和GC-MS分析,MALD-TOF-MS测量和NMR光谱用于确认异构体的结构特征。使用COSY,E-HSQC,HSQC-TOCSY,HMBC和H2BC技术分配每种异构体糖的(1)H和(13)C NMR信号。这些异构体被鉴定为α-D-果糖呋喃糖基-(2-> 2)-α-D-吡喃葡萄糖基-(1 <-> 2)-β-D-果糖呋喃糖苷,α-D-果糖呋喃糖基-(2-> 3 )-β-D-果糖呋喃糖基-(2 <-> 1)-α-D-吡喃葡萄糖苷,α-D-果糖呋喃糖基-(2-> 4)-β-D-果糖呋喃糖基-(2 <-> 1)-α -D-吡喃葡萄糖苷,β-D-果呋喃糖基-(2-> 4)-β-D-呋喃呋喃糖基-(2 <-> 1)-α-D-吡喃葡萄糖苷,β-D-呋喃呋喃糖基-(2-> 3) -α-D-吡喃葡萄糖基-(1
  • Studies on the constituents of Leguminous plants. VII. The structure of triterpenoid saponins from fruits of Gymnocladus chinensis Baillon.
    作者:TAKAO KONOSHIMA、TOKUNOSUKE SAWADA、TAKEATSU KIMURA
    DOI:10.1248/cpb.32.4833
    日期:——
    Three triterpenoid saponins, gymnocladus saponins A (12), B (18) and C (20), were isolated from the fruits of Gymnocladus chinensis BAILLON (Leguminosae). On the basis of chemical and physicochemical evidence, these saponins were characterized as 2β, 23-dihydroxy-3-O-[α-L-arabinopyranosyl (1→6)-β-D-glucopyranosyl] acacic acid 28, 21-lactone (12), 2β, 23-dihydroxy-3-O-[β-D-glucopyranosyl (1→2)-β-D-glucopyranosyl] acacic acid 28, 21-lactone (18) and 2β, 23-dihydroxy-3-O-[β-D-xylopyranosyl (1→2)-α-L-arabinopyranosyl (1→6)-β-D-glucopyranosyl] acacic acid 28, 21-lactone (20).
    从中华雀花(Gymnocladus chinensis BAILLON,豆科)果实中分离出三种三萜皂苷,分别是雀花皂苷A (12)、B (18)和C (20)。根据化学和物理化学的证据,这些皂苷被表征为:2β, 23-二羟基-3-O-[α-L-阿拉伯糖喃糖(1→6)-β-D-葡萄糖喃糖] 酸性28, 21-内酯 (12);2β, 23-二羟基-3-O-[β-D-葡萄糖喃糖(1→2)-β-D-葡萄糖喃糖] 酸性28, 21-内酯 (18);和2β, 23-二羟基-3-O-[β-D-木糖喃糖(1→2)-α-L-阿拉伯糖喃糖(1→6)-β-D-葡萄糖喃糖] 酸性28, 21-内酯 (20)。
  • Saponin and sapogenol. XXXIII. Chemical constituents of the seeds of Vigna angularis (Willd.) Ohwi et Ohashi. (3). Azukisaponins V and VI.
    作者:ISAO KITAGAWA、HUIKANG WANG、MASAYUKI SAITO、MASAYUKI YOSHIKAWA
    DOI:10.1248/cpb.31.683
    日期:——
    The chemical structures of azukisaponins V (1) and VI (5), two of the six oligoglycosidic ingredients of total azukisaponin isolated from azuki beans, the seeds of Vigna angularis (WILLD.) OHWI et OHASHI (Leguminosae), were investigated. By means of photochemical degradation and chemical analyses, the structures of azukisaponins V and VI were elucidated to be 3-O-[α-L-rhamnopyranosyl (1→2)-β-D-glucopyranosyl (1→2)-β-D-glucuronopyranosyl]-soyasapogenol B (1) and 3-O-[β-D-glucopyranosyl (1→2)-β-D-glucuronopyranosyl]-29-O-[β-D-glucopyranosyl (1→6)-β-D-glucuronopyranosyl] azukisapogenol (5), respectively. Azukisaponin VI (5) is the first reported example of a 3, 29-bisdesmoside of an oleanene oligoglycoside.
    研究了从红豆(Vigna angularis (WILLD.) OHWI et OHASHI)中提取的总红豆皂苷的六种寡糖苷成分中的两种:红豆皂苷V(1)和VI(5)的化学结构。通过光化学降解和化学分析,阐明了红豆皂苷V和VI的结构分别为3-O-[α-L-鼠李糖喃基(1→2)-β-D-葡萄糖喃基(1→2)-β-D-葡萄糖醛酸喃基]-大豆皂苷醇B(1)和3-O-[β-D-葡萄糖喃基(1→2)-β-D-葡萄糖醛酸喃基]-29-O-[β-D-葡萄糖喃基(1→6)-β-D-葡萄糖醛酸喃基]红豆皂苷醇(5)。红豆皂苷VI(5)是首次报道的三、二十九双配糖体的鞘脂寡糖苷。
  • Melongoside L and melongoside M, steroidal saponins from Solanum melongena seeds
    作者:Pavel K. Kintia、Stepan A. Shvets
    DOI:10.1016/s0031-9422(00)80843-2
    日期:1985.1
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