13153-11-2 (LAMBDA4-噻吩-1-酮,1lambda4-thietan-1-one)

快速询单

结构式：

LAMBDA4-噻吩-1-酮MOL文件

CAS号：

13153-11-2

中文名称：

LAMBDA4-噻吩-1-酮

英文名称：

1lambda4-thietan-1-one

分子式：

C₃H₆OS

分子量：

90.1441397666931

LAMBDA4-噻吩-1-酮(13153-11-2)名称与标识符

名称

英文别名：

Thietane, 1-oxide;PROPANESULPHONE;1,3-Propanesulfone;Thietane oxide;Thietane S-oxide;Trimethylene sulfoxide;1,3-PROPANESULPHONE;1lambda4-thietan-1-one;2TZH7KB8N8;1;E?-thietan-1-one;BDBM50224813;CHEMBL368734;trimethylensulfoxid;NSC244321;Thietane, 1-oxide (9CI);Propanesulfone;NSC-244321;propane sulfone;13153-11-2;BRN 0104565;Thietane 1-oxide;DTXSID10157099;UNII-2TZH7KB8N8;NSC 244321;Propylthiocyclane sulfoxide;5-17-01-00015 (Beilstein Handbook Reference);EN300-3429293;InChI=1/C3H6OS/c4-5-2-1-3-5/h1-3H;

标识符

MDL：

MFCD01677754

InChIKey：

GINSRDSEEGBTJO-UHFFFAOYSA-N

Inchi：

1S/C3H6OS/c4-5-2-1-3-5/h1-3H2

SMILES：

S1(CCC1)=O

LAMBDA4-噻吩-1-酮(13153-11-2)物化性质

实验特性

PSA : 17.07

计算特性

精确分子量 : 90.01398
氢键供体数量 : 0
氢键受体数量 : 2
可旋转化学键数量 : 0
同位素质量 : 90.01393598g/mol
重原子数量 : 5
复杂度 : 53.9
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 : 1
疏水参数计算参考值（XlogP） : -0.6
拓扑分子极性表面积 : 36.3Å²

LAMBDA4-噻吩-1-酮(13153-11-2)推荐厂家更多厂家(3)

公司名称	手机号/电话	联系人	QQ	微信	询单
金锦乐（湖南）化学有限公司		金锦乐	1226360695		询单

LAMBDA4-噻吩-1-酮(13153-11-2)相关文献

1. Straightforward access to 4-membered sulfurated heterocycles: introducing a strategy for the single and double functionalization of thietane 1-oxide
Laura Carroccia,Leonardo Degennaro,Giuseppe Romanazzi,Corrado Cuocci,Luisa Pisano,Renzo Luisi Org. Biomol. Chem. 2014 12 2180
2. A greener and efficient access to substituted four- and six-membered sulfur-bearing heterocycles
Giovanna Parisi,Leonardo Degennaro,Claudia Carlucci,Modesto de Candia,Piero Mastrorilli,Alexander Roller,Wolfgang Holzer,Cosimo Damiano Altomare,Vittorio Pace,Renzo Luisi Org. Biomol. Chem. 2017 15 5000
3. Conformational analysis. Part 23. A lanthanide-induced shift investigation of some cyclic and acyclic sulfoxides
Raymond J. Abraham,Leonard Pollock,Fernando Sancassan J. Chem. Soc. Perkin Trans. 2 1994 2329
4. Metallacyclic complexes. Part 4. Synthesis of platinathietane-3-oxide complexes, and the single-crystal X-ray structure of [Pt{CH(COPh)S(O)CH(COPh)}(PPh3)2]·2CH2Cl2
William Henderson,Raymond D. W. Kemmitt,Lesley J. S. Prouse,David R. Russell J. Chem. Soc. Dalton Trans. 1990 1853
5. Index pages
J. Chem. Soc. Perkin Trans. 2 1981 A001
6. The preparation and structures of metallathietane-3-oxides and –3,3-dioxides of platinum and palladium: the crystal structures of trans-2,4-dibenzoyl-1,1-bis(triphenylphosphine)platinathietane-3-oxide and trans-2,4-dibenzoyl-1,1-bis(triphenylphosphine)platinathietane-3,3-dioxide
William Henderson,Raymond D. W. Kemmitt,John Fawcett,Lesley J. S. Prouse,David R. Russell J. Chem. Soc. Chem. Commun. 1986 1791
7. The preparation and structures of metallathietane-3-oxides and –3,3-dioxides of platinum and palladium: the crystal structures of trans-2,4-dibenzoyl-1,1-bis(triphenylphosphine)platinathietane-3-oxide and trans-2,4-dibenzoyl-1,1-bis(triphenylphosphine)platinathietane-3,3-dioxide
William Henderson,Raymond D. W. Kemmitt,John Fawcett,Lesley J. S. Prouse,David R. Russell J. Chem. Soc. Chem. Commun. 1986 1791
8. Structural assessment of anhydrous sulfates with high field 33S solid state NMR and first principles calculations
Peter J. Pallister,Igor L. Moudrakovski,Gary D. Enright,John A. Ripmeester CrystEngComm 2013 15 8808
9. Eliminative fission of hydroxythietanes: transition structures for cleavage of 4-membered rings
David J. Young,Charles J. M. Stirling J. Chem. Soc. Chem. Commun. 1987 552