28322-92-1 (吡啶三氧化硫,pyridine sulfur trioxide)

快速询单

结构式：

吡啶三氧化硫MOL文件

CAS号：

28322-92-1

中文名称：

吡啶三氧化硫

英文名称：

pyridine sulfur trioxide

分子式：

C₅H₅NO₃S

分子量：

159.163100004196

吡啶三氧化硫(28322-92-1)名称与标识符

名称

中文别名：

吡啶三氧化硫;三氧化硫吡啶配合物;三氧化硫化合物吡啶;

英文别名：

pyridine sulfur trioxide;pyridine, compound with sulfur trioxide;SULFUR TRIOXIDE COMPD. WITH PYRIDINE;Pyridine-sulfuric anhydride complex;Sulfur trioxide-pyridine complex;Sulfuric anhydride-pyridine complex;Pyridine sulfotrioxide;DTXSID50885349;pyridine; sulfonylideneoxidane;CS-0015119;Sulphur trioxide pyridine;sulfur trioxide-pyridine;Pyridine-sulfur trioxide (1:1);NSC75831;EINECS 248-968-5;NSC 75831;Pyridine sulfonylideneoxidane;AKOS005258855;NS00082792;Pyridine compound with sulfur trioxide (1:1);pyridine;sulfur trioxide;Pyridine-Sulfur Trioxide;Py.SO3;Q7636231;SCHEMBL39580;Sulphur trioxide--pyridine (1:1);s12334;28322-92-1;AS-16050;pyridine sulphur trioxide;Pyridine, compound with sulphur trioxide;Pyridine; compound with GENERIC INORGANIC NEUTRAL COMPONENT;DB-418739;F8881-6763;NSC-75831;SVL47N2N3Y;DB-046946;EINECS 247-683-3;J-524102;UNII-SVL47N2N3Y;SO3.Pyridine;26412-87-3;sulfur trioxide pyridine;Sulphur trioxide pyridine (1:1);Sulfur Trioxide-Pyridine; SO3-Py;MFCD00012437;P0998;J-016414;EC 247-683-3;BCP10411;sulfurtrioxide pyridine;EN300-30095;

标识符

InChIKey：

UDYFLDICVHJSOY-UHFFFAOYSA-N

Inchi：

1S/C5H5N.O3S/c1-2-4-6-5-3-1;1-4(2)3/h1-5H;

SMILES：

S(=O)(=O)=O.N1C=CC=CC=1

吡啶三氧化硫(28322-92-1)物化性质

计算特性

精确分子量 : 158.99901420g/mol
氢键供体数量 : 0
氢键受体数量 : 4
可旋转化学键数量 : 0
同位素质量 : 158.99901420g/mol
重原子数量 : 10
复杂度 : 92.8
同位素原子数量 : 0
确定原子立构中心数量 : 0
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 : 2
拓扑分子极性表面积 : 65.1Å²

吡啶三氧化硫(28322-92-1)国际标准相关数据

EINECS：

248-968-5

吡啶三氧化硫(28322-92-1)推荐厂家更多厂家(4)

公司名称	手机号/电话	联系人	QQ	微信	询单
郑州阿尔法化工有限公司	15324716602 0371-55013243	刘经理	2853979810		询单
金锦乐（湖南）化学有限公司		金锦乐	1226360695		询单

吡啶三氧化硫(28322-92-1)相关文献

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John O. Morley J. Chem. Soc. Perkin Trans. 2 1976 1554
2. Bifunctional mannoside–glucosinolate glycoconjugates as enzymatically triggered isothiocyanates and FimH ligands
G. Cutolo,F. Reise,M. Schuler,R. Nehmé,G. Despras,J. Brekalo,P. Morin,P.-Y. Renard,T. K. Lindhorst,A. Tatibou?t Org. Biomol. Chem. 2018 16 4900
3. Steroid conjugates. Part III. Syntheses of 19-oxygenated dehydro-epi-androsterone sulphates
M. S. Rajagopalan,D. S. H. Smith,A. B. Turner J. Chem. Soc. C 1971 646
4. Synthesis and biological activity of naturally occurring α-glucosidase inhibitors
Duncan J. Wardrop,Samanthi L. Waidyarachchi Nat. Prod. Rep. 2010 27 1431
5. The allyl ether as a protecting group in carbohydrate chemistry. Part 10. Synthesis of 3-O-(β-D-galactopyranosyl 3-sulphate)-2-O-hexadecanoyl-1-O-hexadecyl-L-glycerol, ‘seminolipid’
Roy Gigg J. Chem. Soc. Perkin Trans. 1 1979 712
6. Organic synthesis in the study of terpene-derived oxidation products in the atmosphere
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7. Peptides. Part XXV. The structure and synthesis of human gastrin
J. Beacham,P. H. Bentley,G. W. Kenner,J. K. MacLeod,J. J. Mendive,R. C. Sheppard J. Chem. Soc. C 1967 2520
8. 343. Synthesis of “active sulphate”(adenosine 3′-phosphate 5′-sulphatophosphate)
J. Baddiley,J. G. Buchanan,R. Letters,A. R. Sanderson J. Chem. Soc. 1959 1731
9. Stereoselective syntheses and biological activities of E-series resolvins
Anders Vik,Trond Vidar Hansen Org. Biomol. Chem. 2021 19 705
10. Samarium(II)-mediated 4-exo-trig cyclisations of unsaturated aldehydes. A stereoselective approach to functionalised cyclobutanols
Derek Johnston,Catherine F. McCusker,Kenneth Muir,David J. Procter J. Chem. Soc. Perkin Trans. 1 2000 681