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2-Cyclopenten-1-one, 2-(2-aminophenyl)-3,4-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

912675-91-3

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912675-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 912675-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,6,7 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 912675-91:
(8*9)+(7*1)+(6*2)+(5*6)+(4*7)+(3*5)+(2*9)+(1*1)=183
183 % 10 = 3
So 912675-91-3 is a valid CAS Registry Number.

912675-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-aminophenyl)-3,4-dimethylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-(2-amino)phenyl-3,4-dimethyl-2-cyclopenten-1-one

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:912675-91-3 SDS

912675-91-3Relevant academic research and scientific papers

Synthesis and structures of o-phenylene-bridged Cp/phosphinoamide titanium complexes

Ji Wu, Chun,Hoon Lee, Sang,Yun, Hoseop,Yeoul Lee, Bun

, p. 5638 - 5646 (2006)

Addition of R′2PCl to anilines substituted with di- or trimethylcyclopentadienyl unit at ortho-position affords ortho-phenylene-bridged Me2Cp or Me3Cp/phosophinoamide ligands, 2-(RMe2C5H2)C

Transition metal complexes, catalyst compositions containing the same, and olefin polymerization using the catalyst compositions

-

Page/Page column 32, (2009/05/29)

Provided are a novel transition metal complex where a monocyclopentadienyl ligand to which an amido or alcoxy group is introduced is coordinated, a method of synthesizing the same, and olefin polymerization using the transition metal complex. Compared to

Transition metal complexes, catalyst compositions containing the same, and olefin polymerization using the catalyst compositions

-

Page/Page column 10, (2008/06/13)

Provided are a novel transition metal complex where a monocyclopentadienyl ligand to which an amine-based group is introduced is coordinated, a method of synthesizing the same, and olefin polymerization using the transition metal complex In the novel tran

O-Phenylene-bridged Cp/sulfonamido titanium complexes for ethylene/1-octene copolymerization

Joe, Dae June,Wu, Chun Ji,Bok, Taekki,Lee, Eun Jung,Lee, Choong Hoon,Han, Won-Sik,Kang, Sang Ook,Lee, Bun Yeoul

, p. 4056 - 4062 (2007/10/03)

The Suzuki-coupling reaction of 2-(dihydroxyboryl)-3,4-dimethyl-2- cyclopenten-1-one (1) and 2-(dihydroxyboryl)-3-methyl-2-cyclopenten-1-one (2) with 2-bromoaniline derivatives affords cyclopentenone compounds (3-8) from which cyclopentadiene compounds, 4,6-R′2-2-(2,5-Me 2C5H3)C6H2NH2 (9-11) and 4,6-R′2-2-(2,3,5-Me3C5H 2)C6H2NH2 (12-14) are prepared. After sulfonation of the -NH2 group with p-TsCl, metallation is carried out by successive addition of Ti(NMe2)4 and Me2SiCl2 affording o-phenylene-bridged Cp/sulfonamido titanium dichloride complexes, [4,6-R′2-2-(2,5-Me 2C5H2)C6H2NSO 2C6H4CH3)]TiCl2 (R′ = H, 21; R′ = Me, 22; R′ = F, 23) and [4,6-R′2-2- (2,3,5-Me3C5H)C6H2NSO 2C6H4CH3)]TiCl2 (R′ = H, 24; R′ = Me, 25; R′ = F, 26). The molecular structures of 24 and [2-(2,5-Me2C5H2)C6H 4NSO2C6H4CH3)]Ti(NMe 2)2 (27) are determined by X-ray crystallography. The Cp(centroid)-Ti-N angle in 24 is smaller (100.90°) than that observed for the CGC (constrained-geometry catalyst), [Me2Si(η5- Me4Cp)(NtBu)]TiCl2 (107.6°) indicating a more "constrained feature" in 24 than in the CGC. Complex 24 shows the highest activity among the newly prepared complexes in ethylene/1-octene copolymerization but it is slightly inferior to the CGC in terms of activity, comonomer-incorporation ability, and molecular weight of the obtained polymers. The Royal Society of Chemistry 2006.

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