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Phenol, 2,2'-[(1R,2R)-1,2-cyclohexanediylbis[(methylimino)methylene]]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193824-04-3

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193824-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193824-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,8,2 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 193824-04:
(8*1)+(7*9)+(6*3)+(5*8)+(4*2)+(3*4)+(2*0)+(1*4)=153
153 % 10 = 3
So 193824-04-3 is a valid CAS Registry Number.

193824-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-[trans-(R,R)-1,2-cyclohexanediylbis(N-methylaminomethyl)]-diphenol

1.2 Other means of identification

Product number -
Other names (1R,2R)-1,2-bis[(2-hydroxybenzyl)(methyl)amino]cyclohexane

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:193824-04-3 SDS

193824-04-3Downstream Products

193824-04-3Relevant academic research and scientific papers

A dioxomolybdenum(VI) complex with a new enantiomerically pure tetrahydrosalen ligand

Elias, Horst,Stock, Frank,Roehr, Caroline

, p. 862 - 864 (1997)

The enantiomerically pure tetradentate ligand H2L {2,2′-[trans-(R,R)-1,2-cyclohexanediylbis(N-methyl-aminomethyl)]diphenol} forms a neutral dioxomolybdenum(VI) complex, which was isolated as {2,2′-[trans-(R,R)-1,2-cyclohexanediylbis(N-methylami

Chiral salan aluminium ethyl complexes and their application in lactide polymerization

Du, Hongzhi,Velders, Aldrik H.,Dijkstra, Pieter J.,Sun, Jingru,Zhong, Zhiyuan,Chen, Xuesi,Feijen, Jan

supporting information; experimental part, p. 9836 - 9845 (2010/04/05)

Synthetic routes to aluminium ethyl complexes supported by chiral tetradentate phenoxyamine (salan-type) ligands [Al(OC6H 2(R-O-R4)CH2)2{CH3N(C 6H10)NCH3}-C2H5] (4, 7: R = H; 5, 8: R = Cl; 6, 9: R = CH3) are reported. Enantiomerically pure salan ligands 1-3 with (R,R) configurations at their cyclohexane rings afforded the complexes 4, 5, and 6 as mixtures of two diastereoisomers (a and b). Each diastereoisomer a was, as determined by X-ray analysis, monomeric with a five-coordinated aluminium central core in the solid state, adopting a cis-(O,O) and cis-(Me,Me) ligand geometry. From the results of variabletemperature (VT) 1H NMR in the tern-perature range of 220-335 K, 1H- 1H NOESY at 220K, and diffusion-ordered spectroscopy (DOSY), it is concluded that each diastereoisomer b is also monomeric with a five-coordinated aluminium central core. The geometry is intermediate between square pyramidal with a cis-(O,O), trans-(Me,Me) ligand disposition and trigonal bipyramidal with a rrans-(O,O) and trans(Me,Me) disposition. A slow exchange between these two geometries at 220 K was indicated by 1H-1H NOESY NMR. In the presence of propan-2-ol as an initiator, enantiomerically pure (R,R) complexes 4-6 and their racemic mixtures 7-9 were efficient catalysts in the ring-opening polymerization of lactide (LA). Polylactide materials ranging from isotactically biased (Pm up to 0.66) to medium heterotactic (P r up to 0.73) were obtained from rac-lactide, and syndiotactically biased polylactide (Pr up to 0.70) from wicso-lactide. Kinetic studies revealed that the polymerization of (S,S)-LA in the presence of 4/propan-2-ol had a much higher polymerization rate than (R,R)-LA polymerization (kss/kRR = 10.1).

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