7283-10-5 ((alpha-D-Pyranose-form-Talose,)

快速询单

结构式：

alpha-D-Pyranose-form-Talose,MOL文件

CAS号：

7283-10-5

英文名称：

alpha-D-Pyranose-form-Talose,

分子式：

C₆H₁₂O₆

分子量：

180.155882835388

alpha-D-Pyranose-form-Talose,(7283-10-5)名称与标识符

名称

英文别名：

alpha-D-Pyranose-form-Talose,;alpha-D-Pyranose-Mannose;beta-D-Pyranose-form-Talose,;beta-D-Pyranose-Glucose;beta-D-Pyranose-Mannose;D-(+)-glupyranose;D-glucose;D-Mannose;galactose;glucose;hexapyranose;hexopyranose;L-Mannose;Mannose;ss-D-Altrose;beta-D-altropyranose;beta-D-altrose;b-D-Alt;beta-D-altro-hexopyranose;CHEBI:148773;WURCS=2.0/1,1,0/[a1222h-1b_1-5]/1/;7283-10-5;UNII-CN4MRR6TBH;(2R,3S,4R,5R,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol;(2R,3S,4R,5S,6R)-6-(hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol;.BETA.-D-ALTROPYRANOSE;A-D-Altropyranose;(2R,3S,4R,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol;MFCD00075620;CN4MRR6TBH;SCHEMBL8931260;

标识符

MDL：

MFCD00075620

InChIKey：

WQZGKKKJIJFFOK-DGPNFKTASA-N

Inchi：

1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4-,5+,6-/m1/s1

SMILES：

O1[C@H]([C@H]([C@@H]([C@@H]([C@H]1CO)O)O)O)O

alpha-D-Pyranose-form-Talose,(7283-10-5)物化性质

计算特性

精确分子量 : 180.06338810g/mol
氢键供体数量 : 5
氢键受体数量 : 6
可旋转化学键数量 : 1
同位素质量 : 180.06338810g/mol
重原子数量 : 12
复杂度 : 151
同位素原子数量 : 0
确定原子立构中心数量 : 5
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） : -2.6
拓扑分子极性表面积 : 110Å²

alpha-D-Pyranose-form-Talose,(7283-10-5)相关文献

1. 351. The isopropylidene derivatives of D-altrose and 1 : 6-anhydro-β-D-altrose
F. H. Newth,L. F. Wiggins J. Chem. Soc. 1950 1734
2. 87. O-toluene-p-sulphonyl derivatives of 1 : 6-anhydro-β-D-altrose and their behaviour towards alkali.
F. H. Newth J. Chem. Soc. 1956 441
3. 87. O-toluene-p-sulphonyl derivatives of 1 : 6-anhydro-β-D-altrose and their behaviour towards alkali.
F. H. Newth J. Chem. Soc. 1956 441
4. 288. Derivatives of 3-acetamido-3-deoxy-D-altrose and their conversion into 2-acetamido-2-deoxy-D-ribose
Bruce Coxon,L. Hough J. Chem. Soc. 1961 1463
5. 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
6. Chemoenzymatic synthesis of carbasugars from iodobenzene
Derek R. Boyd,Narain D. Sharma,Nuria M. Llamas,John F. Malone,Colin R. O'Dowd,Christopher. C. R. Allen Org. Biomol. Chem. 2005 3 1953
7. Synthesis of 5-thio-D-allose and 5-thio-D-altrose
Neil A. Hughes J. Chem. Soc. Chem. Commun. 1979 319
8. Synthesis of trifluoromethyl analogue of L-fucose and 6-deoxy-D-altrose
Romesh C. Bansal,Barbara Dean,Sen-itiroh Hakomori,Tatsushi Toyokuni J. Chem. Soc. Chem. Commun. 1991 796
9. New synthetic applications of sialic acid aldolase, a useful catalyst for KDO synthesis. Relation between substrate conformation and enzyme stereoselectivity
Udo Kragl,Astrid G?dde,Christian Wandrey,Nadège Lubin,Claudine Augé J. Chem. Soc. Perkin Trans. 1 1994 119
10. 655. Structure and reactivity of anhydro-sugars. Part I. Branched-chain sugars. Part I. Action of diethylmagnesium on methyl 2: 3-anhydro 4: 6-O-benzylidene-α-D-mannoside
A. B. Foster,W. G. Overend,M. Stacey,G. Vaughan J. Chem. Soc. 1953 3308

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7283-10-5 ((alpha-D-Pyranose-form-Talose,)

alpha-D-Pyranose-form-Talose,(7283-10-5)名称与标识符

名称

标识符

alpha-D-Pyranose-form-Talose,(7283-10-5)物化性质

计算特性

alpha-D-Pyranose-form-Talose,(7283-10-5)相关文献

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