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phenol, 2-[[bis(2-hydroxyethyl)amino]methyl]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96182-90-0

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96182-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96182-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,8 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96182-90:
(7*9)+(6*6)+(5*1)+(4*8)+(3*2)+(2*9)+(1*0)=160
160 % 10 = 0
So 96182-90-0 is a valid CAS Registry Number.

96182-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[bis(2-hydroxyethyl)amino]methyl]-4-methylphenol

1.2 Other means of identification

Product number -
Other names 2-{[bis(2-hydroxyethyl)amino]methyl}-4-methylphenol

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:96182-90-0 SDS

96182-90-0Downstream Products

96182-90-0Relevant academic research and scientific papers

Zn(II) Complex Catalyzed Coupling Aquathermolysis of Water-Heavy Oil-Methanol at Low Temperature

Chen, Gang,Yuan, Weihua,Yan, Jiao,Meng, Mei,Guo, Zheng,Gu, Xuefan,Zhang, Jie,Qu, Chengtun,Song, Hua,Jeje, Ayodeji

, p. 197 - 202 (2018)

A Zn(II) coordination complex was synthesized, characterized, and used for catalytic aquathermolysis of heavy oil at low temperatures for the first time. The effects of water content and catalyst concentration on aquathermolysis were investigated. And then a tri-component coupling aquathermolysis of waterheavy oil-methanol was designed and the reaction conditions were investigated. With the catalyst and methanol, the reaction occurred at temperatures as low as 180°C. The viscosity of the product was also substantially reduced from around 24 400 to 6420 mPa s by the decomposition of the large hydrocarbon molecules.

Complexes of cis-dioxomolybdenum(VI) with unsymmetrical tripodal NO3-donor ligands: Synthesis, characterization and catalytic applications

Kurapati, Sathish Kumar,Maloth, Swamy,Pal, Samudranil

supporting information, p. 66 - 73 (2015/03/30)

A series of cis-dioxomolybdenum(VI) complexes of general formula cis-[MoO2(HLn)] (1-4) have been synthesized in 80-85% yields by reacting equimolar amounts of [MoO2(acac)2] (acac- = acetylacetonate) with 2,2′-(2-hydroxy-3,5-R1,R2-benzylazanediyl)diethanols (H3Ln, n = 1-4) in methanol. Characterization of the complexes has been performed by elemental analysis, spectroscopic (IR, UV-Vis, 1H and 13C NMR) and electrochemical measurements. The molecular structures of all four complexes have been determined by single-crystal X-ray diffraction studies. In each of these analogous complexes, the metal centre is in a distorted octahedral NO5 coordination sphere assembled by the single edge shared 5,5,6-membered chelate rings forming NO3-donor (HLn)2- and two cis oriented oxo groups. Crystal structures of the complexes reveal formation of discrete centrosymmetric dimeric species via a pair of reciprocal intermolecular O-HO hydrogen bonding interactions. Spectroscopic data of all the complexes are consistent with their molecular structures. In the cyclic voltammograms, the redox-active complexes display a quasi-reversible to irreversible metal centred reduction with the cathodic peak potential in the range -0.92 to -1.12 V (versus Ag/AgCl). All the complexes have been evaluated for their catalytic activities in oxidative bromination reactions of styrene and salicylaldehyde and in benzoin oxidation reaction.

Reaction on a solid surface - A simple, economical, and efficient Mannich reaction of azacrown ethers over graphite

Sharghi, Hashem,Khalifeh, Reza

, p. 426 - 434 (2008/09/20)

Graphite brings about a rapid Mannich reaction with a range of activated and unactivated phenolic compounds such as p-cresol and p-nitrophenol. The reactions are carried out with azacrown ether and paraformaldehyde in solvent-free conditions at 100 °C for 20-30 min. The graphite powder can be reused up to three times after simple washing with acetone.

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