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Trichloro-[(S)-1-(4-fluoro-phenyl)-ethyl]-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

170876-30-9

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170876-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170876-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,8,7 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 170876-30:
(8*1)+(7*7)+(6*0)+(5*8)+(4*7)+(3*6)+(2*3)+(1*0)=149
149 % 10 = 9
So 170876-30-9 is a valid CAS Registry Number.

170876-30-9Upstream product

170876-30-9Relevant academic research and scientific papers

High-molecular-weight polyquinoxaline-based helically chiral phosphine (PQXphos) as chirality-switchable, reusable, and highly enantioselective monodentate ligand in catalytic asymmetric hydrosilylation of styrenes

Yamamoto, Takeshi,Yamada, Tetsuya,Nagata, Yuuya,Suginome, Michinori

supporting information; experimental part, p. 7899 - 7901 (2010/08/05)

A polyquinoxaline-based helical polymer ligand bearing both helical-sense-determining chiral side chains and coordinating diarylphosphino side chains exhibits solvent-dependent formation of P- or M-helical structures, with which either the S- or R-hydrosilylation product was obtained with high (>93% enantiomeric excess) enantioselectivities.

Helical poly(quinoxaline-2,3-diyl)s bearing metal-binding sites as polymer-based chiral ligands for asymmetric catalysis

Yamamoto, Takeshi,Suginome, Michinori

scheme or table, p. 539 - 542 (2009/04/14)

Living it up: Helical polyquinoxalines with single and multiple metal-binding sites, prepared by living polymerization of o-diisocyanobenzenes, are used in the asymmetric hydrosilylation of styrenes, resulting in comparable enantioselectivities to those obtained by low-molecular-weight catalyst systems (up to 87% ee, stereochemistry was determined by a chiral initiator) and a turnover number of almost 1000. (Chemical Equation Presented).

Asymmetric hydrosilylation of styrenes by use of new chiral phosphoramidites

Li, Xinsheng,Song, Jianan,Xu, Dongcheng,Kong, Lichun

, p. 925 - 931 (2008/12/20)

New chiral phosphoramidites were synthesized from chiral unsymmetrical amines and BINOL in good yields. Enantioselective hydrosilylation of styrenes with trichlorosilane in the presence of palladium complexes of these ligands provided chiral silanes in medium to high yields. Oxidation of these chiral silanes with hydrogen peroxide gave the corresponding chiral secondary alcohols in up to 97% ee. Georg Thieme Verlag Stuttgart.

Synthesis of (β-N-sulfonylaminoalkyl)phosphines and their use in palladium-mediated asymmetric synthesis

Sakuraba,Okada,Morimoto,Achiwa

, p. 927 - 934 (2007/10/02)

A series of (β-N-sulfonylaminoalkyl)phosphine ligands has been developed and employed for asymmetric palladium-catalyzed hydrosilylation and Heck-type hydroarylation, affording up to 72% ee and 90% yield.

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