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Silane, [(2,5-dimethylphenyl)methyl]trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62346-91-2

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62346-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62346-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,4 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62346-91:
(7*6)+(6*2)+(5*3)+(4*4)+(3*6)+(2*9)+(1*1)=122
122 % 10 = 2
So 62346-91-2 is a valid CAS Registry Number.

62346-91-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,5-dimethylphenyl)methyl-trimethylsilane

1.2 Other means of identification

Product number -
Other names 2,5-Me2C6H3CH2SiMe3

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62346-91-2 SDS

62346-91-2Downstream Products

62346-91-2Relevant academic research and scientific papers

Ir-Catalyzed Asymmetric and Regioselective Hydrogenation of Cyclic Allylsilanes and Generation of Quaternary Stereocenters via the Hosomi-Sakurai Allylation

Rabten, Wangchuk,Margarita, Cristiana,Eriksson, Lars,Andersson, Pher G.

supporting information, p. 1681 - 1685 (2018/01/05)

A number of cyclic dienes containing the allylsilane moiety were prepared by a Birch reduction and subjected to iridium-catalyzed regioselective and asymmetric hydrogenation, which provided chiral allylsilanes in high conversion and enantiomeric excess (up to 99 % ee). The compounds were successively used in the Hosomi–Sakurai allylation with various aldehydes employing TiCl4 as Lewis acid, providing adducts with two additional stereogenic centers in excellent diastereoselectivity.

Synthesis and structures of the dinuclear tin(II) complexes [R = Ph, X(Z) = CPh; R = SiMe3, X(Z) = PPh2] and of related compounds

Hitchcock, Peter B.,Lappert, Michael F.,Linnolahti, Mikko,Severn, John R.,Uiterweerd, Patrick G.H.,Wang, Zhong-Xia

experimental part, p. 3487 - 3499 (2010/01/15)

Tin(II) compounds containing the ligands [CH(C6H3Me2-2,5)C(But) NSiMe3]- (≡ L1), [CH(Ph)C(Ph)NSiMe3]- (≡L2), [CH(SiMe3)P(Ph)2NSiMe3]- (≡ L3), {A figure is presented} (≡ L4), [C(Ph)C(Ph)NSiMe3]2- (≡ L5), and [C(SiMe3)P(Ph)2NSiMe3]2- (≡ L6) are reported: the transient SnBr(L1) (1) and SnBr(L2) (2), Sn(L1)2 (3) [P.B. Hitchcock, J. Hu, M.F. Lappert, M. Layh, J.R. Severn, J. Chem. Soc., Chem. Commun. (1997) 1189], the labile Sn(L2)2 (4), [Sn(L5)]2 (5), SnCl(L3) (6), Sn(L3)2 (7), [Sn(L6)]2 (8), Sn(L4)2 (9) and Pb(L4)2 (10). They were prepared from (i) SnBr2 and K(L1) (1, 3) or K(L2) (2, 4, 5); (ii) SnCl2 and Li(L3) (6-9); or (iii) PbCl2 and Li(L4) (10). Each of 1, 3 and 5-10 has been characterised by multinuclear NMR spectra; 3, 5, 6, 8, 9 and 10 by EI-mass spectra, but only 3, 5, 8, 9 and 10 were isolated pure and furnished X-ray quality crystals. Of greatest novelty are the title binuclear fused tricyclic ladder-like compounds 5 and 8. Quantum chemical calculations, on alternative pathways to 5 from 2 and to 8 from 7, are reported.

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