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2-Butanone, 3-(ethylamino)-3-methyl- (7CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89854-85-3

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89854-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89854-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,5 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89854-85:
(7*8)+(6*9)+(5*8)+(4*5)+(3*4)+(2*8)+(1*5)=203
203 % 10 = 3
So 89854-85-3 is a valid CAS Registry Number.

89854-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(ethylamino)-3-methyl-2-butanone

1.2 Other means of identification

Product number -
Other names 2-Methyl-2-ethylamino-butanon-(3)

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:89854-85-3 SDS

89854-85-3Downstream Products

89854-85-3Relevant academic research and scientific papers

Imino-amido Hf and Zr complexes: Synthesis, isomerization, and olefin polymerization

Froese, Robert D. J.,Jazdzewski, Brian A.,Klosin, Jerzy,Kuhlman, Roger L.,Theriault, Curt N.,Welsh, Dean M.,Abboud, Khalil A.

experimental part, p. 251 - 262 (2011/03/17)

New hafnium and zirconium imino-amido complexes containing trimethylethylidene bridging groups are reported. Investigation into the thermal stability of these complexes revealed that they undergo facile rearrangement of the ligand backbone at 80 °C to produce isomeric imino-amido complexes. Mechanistic experiments and DFT calculations indicate that this isomerization reaction proceeds via a direct 1,2-methyl shift rather than a multistep mechanism involving the metal center. The initial imino-amido complexes (pre isomerization) exhibit high ethylene/1-octene copolymerization activities and generate polymers with very high molecular weights and relatively low comonomer contents. On the other hand, the isomerized complexes display significantly lower polymerization activities and give polymers with lower molecular weights and broad molecular weight distributions, indicative of multisite behavior.

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