13752-83-5 (樹膠糖酸,ARABIC ACID)

快速询单

结构式：

樹膠糖酸MOL文件

CAS号：

13752-83-5

中文名称：

樹膠糖酸

英文名称：

ARABIC ACID

分子式：

C₅H₁₀O₆

分子量：

166.129302501678

樹膠糖酸(13752-83-5)名称与标识符

名称

中文别名：

樹膠糖酸;阿拉伯糖酸;D-阿拉伯酸;

英文别名：

Arabinonic acid;D-Arabinonic acid;1,4-D-XYLOBIOSE;C01630;D-xylobiose;D-xylonic acid;D-Xylonsaeure;l-Xylonsaeure;xylonic acid;Xylonsaeure;Arabonicacid;ARABINOIC ACID;D-Arabonic acid;D-Arabinoic Acid;(2R,4R)-2,3,4-Trihydroxyglutaric acid;(2R,4R)-2,3,4-Trihydroxypentanedioic acid;ARABIC ACID;Arabonic acid;SCHEMBL192117;E38ABBA6-D029-42A8-9CBE-FCEF81C541C3;arbonic acid;488-30-2;Arabinonate;22373-09-7;Arabinonic acid, DL-;32609-14-6;QXKAIJAYHKCRRA-JJYYJPOSSA-N;6MB7RT6FS7;4F3DFQ2NA3;UNII-4F3DFQ2NA3;D8T;C00878;J-018803;CHEBI:20912;(2S,3R,4R)-2,3,4,5-tetrahydroxypentanoic acid;D-Arabonate;13752-83-5;Q27109364;DTXSID3074991;ARABINIC ACID;ARABINOICACID=ARABONSRE;

标识符

MDL：

MFCD01310213

InChIKey：

QXKAIJAYHKCRRA-JJYYJPOSSA-N

Inchi：

1S/C5H10O6/c6-1-2(7)3(8)4(9)5(10)11/h2-4,6-9H,1H2,(H,10,11)/t2-,3-,4+/m1/s1

SMILES：

O[C@@H]([C@@H](C(=O)O)O)[C@@H](CO)O

樹膠糖酸(13752-83-5)物化性质

计算特性

精确分子量 : 166.04773803g/mol
氢键供体数量 : 5
氢键受体数量 : 6
可旋转化学键数量 : 4
同位素质量 : 166.04773803g/mol
重原子数量 : 11
复杂度 : 135
同位素原子数量 : 0
确定原子立构中心数量 : 3
不确定原子立构中心数量 : 0
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） : -2.7
拓扑分子极性表面积 : 118Å²

樹膠糖酸(13752-83-5)合成路线

合成路线：1 步

反应条件：

1.1R:H2O2, C:Au, S:H2O, 10 min, 120°C, 5 bar

参考文献：

Microwave-assisted base-free oxidation of glucose on gold nanoparticle catalysts

By Rautiainen, Sari et al, Catalysis Communications, 2016, 74, 115-118

樹膠糖酸(13752-83-5)相关文献

1. Successive C1–C2 bond cleavage: the mechanism of vanadium(v)-catalyzed aerobic oxidation of d-glucose to formic acid in aqueous solution
Muge Niu,Yucui Hou,Weize Wu,Shuhang Ren,Ru Yang Phys. Chem. Chem. Phys. 2018 20 17942
2. 191. The constitution of arabic acid. Part V. Methylated arabic acid
F. Smith J. Chem. Soc. 1940 1035
3. Oxidative cleavage of polysaccharides by a termite-derived superoxide dismutase boosts the degradation of biomass by glycoside hydrolases
Jo?o Paulo L. Franco Cairo,Fernanda Mandelli,Robson Tramontina,David Cannella,Alessandro Paradisi,Luisa Ciano,Marcel R. Ferreira,Marcelo V. Liberato,Lívia B. Brenelli,Thiago A. Gon?alves,Gisele N. Rodrigues,Thabata M. Alvarez,Luciana S. Mofatto,Marcelo F. Carazzolle,José G. C. Pradella,Adriana F. Paes Leme,Ana M. Costa-Leonardo,Mário Oliveira-Neto,André Damasio,Gideon J. Davies,Claus Felby,Paul H. Walton,Fabio M. Squina Green Chem. 2022 24 4845
4. 153. The constitution of arabic acid. Part I. The isolation of 3-d-galactosido-l-arabinose
F. Smith J. Chem. Soc. 1939 744
5. 153. The constitution of arabic acid. Part I. The isolation of 3-d-galactosido-l-arabinose
F. Smith J. Chem. Soc. 1939 744
6. 353. The constitution of arabic acid. Part II. Degraded arabic acid
F. Smith J. Chem. Soc. 1939 1724
7. Radiation chemistry of carbohydrates. Part 14. Hydroxyl radical induced oxidation of D-glucose in oxygenated aqueous solution
Man Nien Schuchmann,Clemens von Sonntag J. Chem. Soc. Perkin Trans. 2 1977 1958
8. Catalytic oxidation of rare sugars over gold catalysts
Bright T. Kusema,Dmitry Yu. Murzin Catal. Sci. Technol. 2013 3 297
9. 14. The constitution of arabic acid. Part III. The isolation of methyl heptamethyl aldobionate from methylated degraded arabic acid
J. Jackson,F. Smith J. Chem. Soc. 1940 74
10. VII.—Researches on the gums of the arabin group. Part I. Arabic acid; its composition and the products of its decomposition
C. O'Sullivan J. Chem. Soc. Trans. 1884 45 41

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