1886-75-5 ((propane, 2-[(1,1-dimethylethyl)sulfonyl]-2-methyl-)

快速询单

结构式：

propane, 2-[(1,1-dimethylethyl)sulfonyl]-2-methyl-MOL文件

CAS号：

1886-75-5

英文名称：

propane, 2-[(1,1-dimethylethyl)sulfonyl]-2-methyl-

分子式：

C₈H₁₈O₂S

分子量：

178.292321681976

propane, 2-[(1,1-dimethylethyl)sulfonyl]-2-methyl-(1886-75-5)名称与标识符

名称

英文别名：

propane, 2-[(1,1-dimethylethyl)sulfonyl]-2-methyl-;2-tert-butylsulfonyl-2-methylpropane;Ditert-butyl sulfone;2-((1,1-Dimethylethyl)-sulphonyl)-2-methylpropane;Di-tert-Butyl sulfone;Di-tert-butyl sulphone;tert-Butyl Sulfone;

标识符

InChIKey：

SPJQDMKTFSPPLO-UHFFFAOYSA-N

Inchi：

1S/C8H18O2S/c1-7(2,3)11(9,10)8(4,5)6/h1-6H3

SMILES：

S(C(C)(C)C)(C(C)(C)C)(=O)=O

propane, 2-[(1,1-dimethylethyl)sulfonyl]-2-methyl-(1886-75-5)物化性质

实验特性

PSA : 34.14
折射率 : 1.4433 (estimate)
沸点 : 247.85°C
熔点 : 129.9°C
密度 : 1.0086 (estimate)

计算特性

精确分子量 : 178.10284

propane, 2-[(1,1-dimethylethyl)sulfonyl]-2-methyl-(1886-75-5)相关文献

1. Reactivity of thionitrate esters: putative intermediates in nitrovasodilator activity
Jennifer D. Artz,Kexin Yang,Jodi Lock,Cristina Sanchez,Brian M. Bennett,Gregory R. J. Thatcher Chem. Commun. 1996 927
2. Synthesis and characterization of enantiopure chiral NH2/SO palladium complexes
Nazaret Moreno-Rodriguez,L. Gabriel Borrego,Rocío Recio,Victoria Valdivia,M. Carmen Nicasio,Eleuterio álvarez,Noureddine Khiar,Inmaculada Fernández Org. Biomol. Chem. 2023 21 5827
3. Synthesis and characterization of enantiopure chiral NH2/SO palladium complexes
Nazaret Moreno-Rodriguez,L. Gabriel Borrego,Rocío Recio,Victoria Valdivia,M. Carmen Nicasio,Eleuterio álvarez,Noureddine Khiar,Inmaculada Fernández Org. Biomol. Chem. 2023 21 5827
4. Nickel-catalysed substitutions of aryl tert-butyl sulfones with organometallic reagents: synthesis of ortho-substituted unsymmetrical biaryls
Jonathan Clayden,J. Jonathan A. Cooney,Marc Julia J. Chem. Soc. Perkin Trans. 1 1995 7
5. ortho-Substituted unsymmetrical biaryls from aryl tert-butyl sulfones
Jonathan Clayden,Marc Julia J. Chem. Soc. Chem. Commun. 1993 1682
6. Synthetic studies related to the esperamicin/calicheamicin aglycone: efficient construction of a homochiral oxabicyclo [7 : 3 : 1] analogue from D-xylose
Isabelle Dancy,Troels Skrydstrup,Christophe Crévisy,Jean-Marie Beau J. Chem. Soc. Chem. Commun. 1995 799
7. A truce on the Smiles rearrangement: revisiting an old reaction—the Truce–Smiles rearrangement
Timothy J. Snape Chem. Soc. Rev. 2008 37 2452
8. Allylic sulfones as allyl anion equivalents: homoallylic alcohols from metal catalysed reactions of sulfones with aldehydes and ketones
Jonathan Clayden,Marc Julia J. Chem. Soc. Chem. Commun. 1994 1905
9. Homoallylic alcohols from samarium diiodide-mediated coupling of allylic sulfones with carbonyl compounds
Jonathan Clayden,Marc Julia J. Chem. Soc. Chem. Commun. 1994 2261

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