3149-68-6 (甲基-Α-D-吡喃葡糖苷,Methyl D-Glucopyranoside)

快速询单

结构式：

甲基-Α-D-吡喃葡糖苷MOL文件

CAS号：

3149-68-6

中文名称：

甲基-Α-D-吡喃葡糖苷

英文名称：

Methyl D-Glucopyranoside

分子式：

C₇H₁₄O₆

分子量：

194.182463169098

甲基-Α-D-吡喃葡糖苷(3149-68-6)名称与标识符

名称

中文别名：

1-甲基-α-D-葡萄糖苷;甲基-Alpha-D-吡喃葡糖苷;甲基-Α-D-吡喃葡糖苷;

英文别名：

(2R,3S,4S,5R)-2-(Hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol;D-Glucopyranoside,methyl;(+)-1-O-methyl glucopyranoside;1-O-Methyl-D-glucopyranose;1-O-methyl-D-glucopyranoside;Glucosidizer 100;Methyl D-glucopyranoside;methyl glucopyranoside;Methyl glucoside;Sta-Meg 104;Sta-Meg 106;HOVAGTYPODGVJG-WLDMJGECSA-N;EINECS 221-581-9;NS00082160;GEO-MEG 365;Glucopyranoside, methyl, D-;DTXSID4027523;54L5T38NI8;3149-68-6;CHEBI:37657;methyl-d-glucopyranoside;D-Glucopyranoside, methyl;(2R,3S,4S,5R)-tetrahydro-2-(hydroxymethyl)-6-methoxy-2H-pyran-3,4,5-triol;UNII-54L5T38NI8;Q6824001;J-500989;Methyl D-glucoside;AKOS006237848;Methylglykosid;Sta-Meg 200;(2R,3S,4S,5R)-2-(hydroxymethyl)-6-methoxyoxane-3,4,5-triol;SCHEMBL78632;

标识符

InChIKey：

HOVAGTYPODGVJG-WLDMJGECSA-N

Inchi：

1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6-,7?/m1/s1

SMILES：

O1C([C@@H]([C@H]([C@@H]([C@H]1CO)O)O)O)OC

甲基-Α-D-吡喃葡糖苷(3149-68-6)物化性质

实验特性

LogP : -2.56730
PSA : 99.38000
折射率 : 1.548
沸点 : 389.1±42.0 °C at 760 mmHg
熔点 : Not available
蒸气压 : 0.0±2.0 mmHg at 25°C
闪点 : 189.1±27.9 °C
密度 : 1.5±0.1 g/cm3

计算特性

精确分子量 : 194.079
氢键供体数量 : 4
氢键受体数量 : 6
可旋转化学键数量 : 2
同位素质量 : 194.079
重原子数量 : 13
复杂度 : 163
同位素原子数量 : 0
确定原子立构中心数量 : 4
不确定原子立构中心数量 : 1
确定化学键立构中心数量 : 0
不确定化学键立构中心数量 : 0
共价键单元数量 : 1
疏水参数计算参考值（XlogP） : _2.2
拓扑分子极性表面积 : 99.4A^2

甲基-Α-D-吡喃葡糖苷(3149-68-6)安全信息

安全说明： H303+H313+H333
危害声明：H303+H313+H333
警示性声明：P264+P280+P305+P351+P338+P337+P313
储存条件： storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
信号词： warning

甲基-Α-D-吡喃葡糖苷(3149-68-6)推荐厂家更多厂家(5)

公司名称	手机号/电话	联系人	QQ	询单
上海瀚思化工有限公司	18939883912 021-34536277	顾经理	3003949364	询单
金锦乐（湖南）化学有限公司		金锦乐	1226360695	询单
江苏艾康生物医药研发有限公司	18795912720 025-66061636	杨情情	3004779232	询单
上海麦克林生化科技股份有限公司	15221275939 021-50706066	沈经理	269348414	询单
上海源叶生物科技有限公司	15026964105 15026964105	汤思磊	2881489226	询单

甲基-Α-D-吡喃葡糖苷(3149-68-6)相关文献

1. 162. Methylation of β-methylglucopyranoside and αβ-methylxylopyranosides by thallous hydroxide and methyl iodide
C. C. Barker,E. L. Hirst,J. K. N. Jones J. Chem. Soc. 1946 783
2. 11B NMR studies on complexation of borate with linear and crosslinked polysaccharides
Kazuhisa Yoshimura,Yoshinobu Miyazaki,Shinichi Sawada,Hirohiko Waki J. Chem. Soc. Faraday Trans. 1996 92 651
3. Directional liquefaction coupling fractionation of lignocellulosic biomass for platform chemicals
Junming Xu,Xinfeng Xie,Jingxin Wang,Jianchun Jiang Green Chem. 2016 18 3124
4. 636. Mechanism of reactions in the sugar series. Part IV. The structure of the carbonium ions formed in the acid-catalysed solvolysis of glucopyranosides
Barbara E. C. Banks,Yvonne Meinwald,A. J. Rhind-Tutt,I. Sheft,C. A. Vernon J. Chem. Soc. 1961 3240
5. Assignment of 13C and 1H resonances of methyl groups in the tri-O-methyl derivatives of methyl pentopyranosides; some observations on the methoxy 13C chemical shifts
Saeed A. Abbas,Alan H. Haines,Alan G. Wells J. Chem. Soc. Perkin Trans. 1 1976 1351
6. 525. Sugar nitrates. Part I. Removal of nitrate and toluene-p-sulphonyl groups from esters of substituted methyl-D-glucosides
E. G. Ansell,John Honeyman J. Chem. Soc. 1952 2778
7. Synthesis of polyglycocarbonates through polycondensation of glucopyranosides with CO2
Debasis Pati,Zuliang Chen,Xiaoshuang Feng,Nikos Hadjichristidis,Yves Gnanou Polym. Chem. 2017 8 2640
8. 732. The preparation and properties of some alkyl β-D-glucopyranoside tetranitrates
D. M. Shepherd J. Chem. Soc. 1953 3635
9. Synthesis and characterization of 3-O-esters of N-acetyl-d-glucosamine derivatives as organogelators
Anji Chen,Lalith P. Samankumara,Consuelo Garcia,Kristen Bashaw,Guijun Wang New J. Chem. 2019 43 7950
10. The chemistry of ribose and its derivatives. Part V. The synthesis of methyl ethers by partial methylation
G. R. Barker,T. M. Noone,D. C. C. Smith,J. W. Spoors J. Chem. Soc. 1955 1327