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Benzene, 2-bromo-3,5-bis(1,1-dimethylethyl)-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16358-71-7

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16358-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16358-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,5 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16358-71:
(7*1)+(6*6)+(5*3)+(4*5)+(3*8)+(2*7)+(1*1)=117
117 % 10 = 7
So 16358-71-7 is a valid CAS Registry Number.

16358-71-7Relevant academic research and scientific papers

Large-steric hindrance chiral quaternary ammonium salt phase transfer catalyst derived from cinchona alkaloid and synthesis method thereof

-

Paragraph 0054-0058, (2021/10/27)

The invention discloses a large-steric hindrance chiral quaternary ammonium salt phase transfer catalyst derived from cinchona alkaloid. The invention belongs to the technical field of asymmetric catalysis. In the invention, the cinchona alkaloid is disso

Atropisomerism in Diarylamines: Structural Requirements and Mechanisms of Conformational Interconversion

Clayden, Jonathan,Costil, Romain,Duarte, Fernanda,Sterling, Alistair J.

supporting information, p. 18670 - 18678 (2020/08/25)

In common with other hindered structures containing two aromatic rings linked by a short tether, diarylamines may exhibit atropisomerism (chirality due to restricted rotation). Previous examples have principally been tertiary amines, especially those with

Catalytic Asymmetric Hydroalkenylation of Vinylarenes: Electronic Effects of Substrates and Chiral N-Heterocyclic Carbene Ligands

Ho, Chun-Yu,Chan, Chun-Wa,He, Lisi

supporting information, p. 4512 - 4516 (2015/04/14)

An asymmetric tail-to-tail cross-hydroalkenylation of vinylarenes with terminal olefins was achieved by catalysis with NiH complexes bearing chiral N-heterocyclic carbenes (NHCs). The reaction provides branched gem-disubstituted olefins with high enantioselectivity (up to 94% ee) and chemoselectivity (cross/homo product ratio: up to 99:1). Electronic effects of the substituents on the vinylarenes and on the N-aryl groups of the NHC ligands, but not a π,π-stacking mechanism, assist the steric effect and influence the outcome of the cross-hydroalkenylation.

Catalytic enantioselective alkylation of sulfenate anions to chiral heterocyclic sulfoxides using halogenated pentanidium salts

Zong, Lili,Ban, Xu,Kee, Choon Wee,Tan, Choon-Hong

supporting information, p. 11849 - 11853 (2015/02/19)

We report halogenated pentanidiums as phasetransfer catalysts for the asymmetric alkylation of sulfenate anions to various sulfoxides with high enantio selectivities (up to 99% ee) and yields (up to 99%). This approach gives access to enantioenriched heterocyclic sulfoxides that might not be compatible with strong oxidants or organometallic reagents. Computational studies have revealed that the multiple non-covalent interactions such as halogen bonds and nonclassical hydrogen bonds are involved.

Enantioselective copper-catalyzed 1,4-addition of dialkylzincs to enones followed by trapping with allyl iodide derivatives

Kawamura, Kenjiro,Fukuzawa, Hitomi,Hayashi, Masahiko

supporting information; experimental part, p. 640 - 647 (2011/08/06)

Enantioselective copper-catalyzed 1,4-addition of dialkylzincs to enones proceeded in the presence of 0.1 mol% of Cu(OTf)2 and 0.25 mol% of an N,N,P-ligand containing a quinoline moiety to afford the corresponding conjugated adducts in 99%ee. The intermediate zinc enolates were trapped with substituted allyl iodides to give disubstituted ketones with high diastereoselectivity and enantioselectivity.

Synthesis of 2,2c-6-trisubstituted and 2,2c-,6,6--tetrasubstituted diaryl sulfides and diaryl sulfones by copper-promoted coupling and/or ortholithiation

Clayden, Jonathan,Senior, James

scheme or table, p. 2769 - 2772 (2010/02/28)

Stoichiometric copper(I) iodide, in the presence of potassium carbonate and ethylene glycol, promotes the coupling of even highly sterically encumbered 2,6-disubstituted thiophenols and aryl iodides to form hindered diarylsulfides. Hindered diarylsulfones

Phenylthiyl radical complexes of gallium(III), iron(III), and cobalt(III) and comparison with their phenoxyl analogues

Kimura,Bill,Bothe,Weyhermueller,Wieghardt

, p. 6025 - 6039 (2007/10/03)

Three hexadentate, asymmetric pendent arm macrocycles containing a 1,4,7-triazacyclononane-1,4-diacetate backbone and a third, N-bound phenolate or thiophenolate arm have been synthesized. In [L1]3- the third arm is 3,5-di-tert-butyl

Formation of Persistent Benzyl Radicals by Protonation of the Radical Anions of Sterically Hindered Dithiobenzoic Esters

Edler, Ronald,Voss, Juergen

, p. 187 - 192 (2007/10/02)

ESR signals due to a second species are observed besides the spectra of the corresponding radical anions when the methyl ortho-(tert-butyl)dithiobenzoates 1, 4, and 6 are electroreduced in situ in dimethylformamide.It is shown by investigation of model co

Contributions to the Chemistry of Phosphorus,184. - Existence and Properties of a Phosphinidenediphosphirane (R1P)2C=PR2

Baudler, Marianne,Simon, Joachim

, p. 281 - 286 (2007/10/02)

The reaction of K(tBu)P-P(tBu)K with the (dichloromethylene)phosphane 2,4-tBu2-6-MeC6H2P=CCl2 (1) yields the first phosphinidenediphosphirane (tBuP)2C=P-(2,4-tBu2-6-Me-C6H2) (2).Further products are the cyclophosphanes (tBuP)n (n=3,4) as well as the phosp

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