2216-49-1 ((Methyl, triphenyl-)

快速询单

结构式：

Methyl, triphenyl-MOL文件

CAS号：

2216-49-1

英文名称：

Methyl, triphenyl-

分子式：

C₁₉H₁₅

分子量：

243.322405099869

Methyl, triphenyl-(2216-49-1)名称与标识符

名称

英文别名：

Methyl, triphenyl-;Gomberg's trityl;Triphenylcarbon radical;Triphenylmethyl;Triphenylmethyl radical;Trityl radical;Trityl(8CI);DTXSID501316922;2216-49-1;

标识符

InChIKey：

OHSJPLSEQNCRLW-UHFFFAOYSA-N

Inchi：

1S/C19H15/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

SMILES：

[C](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1 |^1:0|

Methyl, triphenyl-(2216-49-1)物化性质

计算特性

精确分子量 : 243.117375478g/mol
氢键供体数量 : 0
氢键受体数量 : 0
可旋转化学键数量 : 3
同位素质量 : 243.117375478g/mol
重原子数量 : 19
复杂度 : 196
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） : 5.3
拓扑分子极性表面积 : 0Å²

Methyl, triphenyl-(2216-49-1)相关文献

1. Tracer studies of transfer reactions. Part 2.—Experiments involving triphenylmethane and vinyl acetate
J. C. Bevington,H. G. Troth Trans. Faraday Soc. 1963 59 127
2. The reaction of triphenylmethyl halides with tributylphosphine and tributylamine in apolar solvents
Péter Huszthy,Gy?ngyi Izsó(née Gergácz),Károly Lempert,Mária Kajtár-Peredy,Miklós Gy?r,Antal Rockenbauer,József Tamás J. Chem. Soc. Perkin Trans. 2 1989 1513
3. The reaction of triphenylmethyl bromide with potassium O-ethyl dithiocarbonate (potassium xanthate) in benzene and cumene. A note of caution on the application of the radical trap dicyclohexylphosphine as a probe for electron-transfer-initiated reactions of triphenylmethyl halides
Péter Huszthy,Gy?ngyi Izsó(née Gergácz),Károly Lempert,Miklós Gy?r,Antal Rockenbauer J. Chem. Soc. Perkin Trans. 2 1990 2009
4. The reaction of triphenylmethyl halides with triphenylphosphine in cumene and tert-butylbenzene
Péter Huszthy,Mária Kajtár-Peredy,Károly Lempert,Judit Hegedüs-Vajda J. Chem. Soc. Perkin Trans. 2 1992 347
5. Playing with organic radicals as building blocks for functional molecular materials
Imma Ratera,Jaume Veciana Chem. Soc. Rev. 2012 41 303
6. Reactions of some p-substituted triphenylmethyl chlorides with alcohols, alkali-metal alcoholates, and tributylamine
Gy?ngyi Izsó(née Gergácz),Péter Huszthy,Károly Lempert,József Fetter,Gyula Simig,József Tamás,Judith Hegedüs-Vajda J. Chem. Soc. Perkin Trans. 2 1989 769
7. The ambident reactivity of triphenylmethyl radicals in hydrogen-abstraction reactions and the mechanism of the base-catalysed rearrangement of (diphenylmethylene)cyclohexadienes (a type of semibenzene) into triphenylmethane
Péter Huszthy,Károly Lempert,Gyula Simig,József Tamás,Judit Hegedüs-Vajda,Gábor Tóth J. Chem. Soc. Perkin Trans. 2 1985 491
8. Radicals in natural product synthesis
Kevin J. Romero,Matthew S. Galliher,Derek A. Pratt,Corey R. J. Stephenson Chem. Soc. Rev. 2018 47 7851
9. The resonance energy of the benzyl radical
M. Szwarc Discuss. Faraday Soc. 1947 2 39
10. 311. The anionic nature of the desyl and the α-benzoylbenzhydryl radical as compared with the cationoid reactivity of the triphenylmethyl radical. the hydrolysis of thio-esters
Youssef Iskander J. Chem. Soc. 1948 1549