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Benzene, 1,1',1'',1'''-(1,3-cyclobutanediylidene)tetrakis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53889-00-2

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53889-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53889-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,8 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53889-00:
(7*5)+(6*3)+(5*8)+(4*8)+(3*9)+(2*0)+(1*0)=152
152 % 10 = 2
So 53889-00-2 is a valid CAS Registry Number.

53889-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,3-tetraphenylcyclobutane

1.2 Other means of identification

Product number -
Other names 1,1,3,3-Tetraphenyl-cyclobutan

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:53889-00-2 SDS

53889-00-2Downstream Products

53889-00-2Relevant academic research and scientific papers

ORGANOSILICON COMPOUND HAVING DIPHENYLETHYL AND METHOXYSILYL AND MAKING METHOD

-

Paragraph 0058; 0059, (2017/04/18)

An organosilicon compound having diphenylethyl and methoxysilyl groups is more readily hydrolyzable than ethoxysilyl-containing organosilicon compounds and generates no hydrogen chloride on use.

Half-sandwich ruthenium(II) complexes of aminophosphines: Synthesis, structures and catalytic applications in C-C coupling reactions between styrenes and diphenyldiazomethane

Priya, Srinivasan,Balakrishna, Maravanji S.,Mobin, Shaikh M.,McDonald, Robert

, p. 227 - 235 (2007/10/03)

The half-sandwich Ru(II) complexes of the type [CpRu(PPh2 N(H)R)(PPh3)Cl], [CpRu(PPh2N(H)R)2Cl] (R=Ph, C6H11) and [CpRu(PPh2N(R′) PPh2-κP,κP)(PPh3)]Cl (R′=Et, nPr, iPr, nBu), were synthesized and the structures of complexes [CpRu(PPh2N(H)Ph)(PPh3) Cl] and [CpRu(PPh2N(H)Ph)2Cl] were confirmed by single crystal X-ray diffraction studies. All ruthenium complexes were employed in the cyclopropanation reaction of styrene derivatives in the presence of diphenyldiazomethane. All complexes afford 1,1,3,3-tetraphenyl cyclobutane along with cyclopropane derivatives; complex, [CpRu(PPh2N(nBu)PPh2-κ P,κP) (PPh3)]Cl shows better selectivity in the formation of 1,1,2-triphenylcyclopropane. In all reactions appreciable amounts of cyclopropanation products and metathesis products, 1,2-diphenylcyclopropane and 1,1-diphenylethene were obtained along with 1,1,3-triphenylpropene derivatives. The variable temperature NMR studies have suggested that the cyclopropanation reactions in the presence of ionic complex, [CpRu(PPh2N(R′)PPh 2-κP,κP)(PPh3)]Cl proceeds via carbene intermediate, [CpRu(=CPh2)(PPh2N(R′) PPh2-κP)(PPh3)]Cl.

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