41546-31-0 (L-木呋喃糖（9CI）,L-Xylofuranose (9CI))

快速询单

结构式：

L-木呋喃糖（9CI）MOL文件

CAS号：

41546-31-0

中文名称：

L-木呋喃糖（9CI）

英文名称：

L-Xylofuranose (9CI)

分子式：

C₅H₁₀O₅

分子量：

150.129902362823

L-木呋喃糖（9CI）(41546-31-0)名称与标识符

名称

英文别名：

L-Xylofuranose (9CI);LXylf;WURCS=2.0/1,1,0/[o121h]/1/;(3S,4S,5S)-5-(hydroxymethyl)oxolane-2,3,4-triol;l-xylo-furanose;L-Xylf;CHEBI:153065;L-xylo-pentofuranose;DTXSID90464293;L-Xylofuranose;C01510;41546-31-0;SCHEMBL4874731;

标识符

InChIKey：

HMFHBZSHGGEWLO-CZBDKTQLSA-N

Inchi：

1S/C5H10O5/c6-1-2-3(7)4(8)5(9)10-2/h2-9H,1H2/t2-,3+,4-,5?/m0/s1

SMILES：

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

L-木呋喃糖（9CI）(41546-31-0)物化性质

计算特性

精确分子量 : 150.05282342g/mol
氢键供体数量 : 4
氢键受体数量 : 5
可旋转化学键数量 : 1
同位素质量 : 150.05282342g/mol
重原子数量 : 10
复杂度 : 117
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 : 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
拓扑分子极性表面积 : 90.2Å²

L-木呋喃糖（9CI）(41546-31-0)相关文献

1. Hydroxy group interactions in stannylated carbohydrates. Structures and thermal stabilities of 5-deoxy-5-C-(Ph3Sn)-1,2-O-isopropylidene-α-D-xylofuranose, 5-deoxy-5-C-(IPh2Sn)-1,2-O-isopropylidene-α-D- and -L-xylofuranose, and 5-deoxy-5-C-(I2PhSn)-1,2-O-isopropylidene-α-D- and -L-xylofuranose
Lynne A. Burnett,Vitor F. Ferreira,R. Alan Howie,Helena Rufino,Janet M. S. Skakle,James L. Wardell,Solange M. S. V. Wardell J. Chem. Soc. Perkin Trans. 1 2002 2288
2. 531. 2 : 4–3 : 5-Diethylidene aldehydo-L-xylose and its derivatives
E. J. Bourne,W. M. Corbett,M. Stacey J. Chem. Soc. 1952 2810
3. A comprehensive review of glycosylated bacterial natural products
Sherif I. Elshahawi,Khaled A. Shaaban,Madan K. Kharel,Jon S. Thorson Chem. Soc. Rev. 2015 44 7591
4. Syntheses of 4-acetamido-4,5-dideoxy-D-xylofuranose and 5-acetamido-5,6-dideoxy-L-talofuranose
J. S. Brimacombe,J. G. H. Bryan J. Chem. Soc. C 1966 1724
5. Asymmetric synthesis. Part II. Stereospecific synthesis of benzylic centres. Some 6-deoxy-5-C-phenylhexose derivatives
T. D. Inch,R. V. Ley,P. Rich J. Chem. Soc. C 1968 1683
6. Sustainable synthesis of CO2-derived polycarbonates from d-xylose
David K. Tran,Ahmed Z. Rashad,Donald J. Darensbourg,Karen L. Wooley Polym. Chem. 2021 12 5271
7. 596. The 2 : 3–4 : 5-diisopropylidene derivatives of aldehydo-L-xylose and L-xylitol
E. J. Bourne,G. P. McSweeney,L. F. Wiggins J. Chem. Soc. 1952 3113
8. 335. 2 : 5-Dimethyl xylofuranose and 2 : 3-dimethyl xylose
George J. Robertson,David Gall J. Chem. Soc. 1937 1600
9. Conversion of C5 carbohydrates into furfural catalyzed by a Lewis acidic ionic liquid in renewable γ-valerolactone
Shurong Wang,Yuan Zhao,Haizhou Lin,Jingping Chen,Lingjun Zhu,Zhongyang Luo Green Chem. 2017 19 3869
10. 303. Partial periodate oxidation of D-glucitol and its borate complex
D. H. Hutson,H. Weigel J. Chem. Soc. 1961 1546