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256441-54-0

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  • (11bS) -4-Phenoxy- dinaphtho[2, 1- d:1', 2'- f] [1, 3, 2] dioxaphosphepin

    Cas No: 256441-54-0

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256441-54-0 Usage

General Description

S-4-phenoxy-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin is a complex chemical compound with a unique molecular structure. It belongs to the class of dioxaphosphepins and is characterized by its phenoxy and dinaphtho components. This chemical is known for its potential applications in the field of organic synthesis, thanks to its diverse reactivity and tunable properties. It is also being studied for its potential use in pharmaceuticals and materials science. However, due to its complex structure and specific properties, further research and analysis are required to fully understand its potential applications and behavior in different environments.

Check Digit Verification of cas no

The CAS Registry Mumber 256441-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,4,4 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 256441-54:
(8*2)+(7*5)+(6*6)+(5*4)+(4*4)+(3*1)+(2*5)+(1*4)=140
140 % 10 = 0
So 256441-54-0 is a valid CAS Registry Number.

256441-54-0SDS

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 PhOP(binaphthoxy)

1.2 Other means of identification

Product number -
Other names rac-1,1'-binaphthyl-2,2'-diyl phenyl phosphite

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:256441-54-0 SDS

256441-54-0Relevant articles and documents

Influence of phosphoramidites in copper-catalyzed conjugate borylation reaction

Sole, Cristina,Bonet, Amadeu,De Vries, Andre H. M.,De Vries, Johannes G.,Lefort, Laurent,Gulyas, Henrik,Fernandez, Elena

, p. 7855 - 7861 (2013/01/16)

Copper(I) has become the preferred metal to catalyze the β-boration of α,β-unsaturated carbonyl compounds, and now we demonstrate that easily accessible monodentate chiral ligands, such as phosphoramidites and phosphites, can be convenient alternative ligands to induce asymmetry in the enantioselective version of this reaction, particularly in the β-boration of α,β-unsaturated imines.

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