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S-2,2'-diMethoxy-3,3'-diphenyl-1,1'-Binaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

212191-84-9

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212191-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 212191-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,1,9 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 212191-84:
(8*2)+(7*1)+(6*2)+(5*1)+(4*9)+(3*1)+(2*8)+(1*4)=99
99 % 10 = 9
So 212191-84-9 is a valid CAS Registry Number.

212191-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3'-diphenyl-2,2'-dimethoxy-1,1'-dinaphthyl

1.2 Other means of identification

Product number -
Other names (R)-3,3'-diphenyl-2,2'-dimethoxy-1,1'-binaphthyl

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:212191-84-9 SDS

212191-84-9Relevant academic research and scientific papers

2,2′-Dimethoxy-1,1′-binaphthyl-3,3′-diboronic acid, a versatile intermediate in the synthesis of 3,3′-diaryl substituted binaphthyl derivatives

Kratky, Petra,Haslinger, Ulrike,Widhalm, Michael

, p. 1319 - 1327 (1998)

2,2′-Dimethoxy-1,1′-binaphthyl-3,3′-diboronic acid was prepared in 48% yield from 2,2′-dimethoxy-1,1′-binaphthyl and used as a key intermediate in Suzuki cross-coupling reactions to yield various 2,2′,3,3′-symmetrically substituted binaphthyl derivatives

Synthesis of (±)-3,3′-diphenyl-2,2′-binaphthol via different routes using Pd and Ni as catalyst respectively

Fu, Zhengjiang,Cao, Xihan,Hao, Guangguo,Shi, Quanqing,Cai, Hu

, p. 831 - 836 (2020/09/09)

3,3′-Biphenyl-2,2′-binaphthols (BINOLs) are precursors of phosphoric acids that are widely used as ligands and catalysts in organic reactions. In this report, two routes for the synthesis of (±)-3,3′-diphenyl BINOLs via (±)-3,3′ bis-halogenated BINOLs int

Enantioselective catalytic conjugate addition of dialkylzinc reagents using copper-phosphoramidite complexes; ligand variation and non-linear effects

Arnold, Leggy A.,Imbos, Rosalinde,Mandoli, Alessandro,De Vries, André H.M.,Naasz, Robert,Feringa, Ben L.

, p. 2865 - 2878 (2007/10/03)

A variety of new chiral phosphoramidites was synthesised and tested in the copper-catalysed enantioselective conjugate addition of diethylzinc to cyclohexenone and chalcone in order to assess the structural features that are important for stereocontrol. A

Synthesis and application of macrocyclic binaphthyl ligands with extended chiral bias

Yan, Yuan-Yong,Widhalm, Michael

, p. 3607 - 3610 (2007/10/03)

Two macrocyclic and one non-cyclic chiral diphosphine ligand containing a 2,2'-bridged binaphthyl unit were synthesized in six steps from (R)-2,2'- dimethoxy-1,1'-binaphthyl in overall yields of 25 and 17%, respectively. The new ligands showed asymmetric inductions of up to 98% e.e. if used in palladium catalyzed allylic alkylation reactions.

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