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1-Propanone, 1-(2,4,6-trimethylphenyl)-, oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153933-73-4

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153933-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153933-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,9,3 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153933-73:
(8*1)+(7*5)+(6*3)+(5*9)+(4*3)+(3*3)+(2*7)+(1*3)=144
144 % 10 = 4
So 153933-73-4 is a valid CAS Registry Number.

153933-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[1-(2,4,6-trimethylphenyl)propylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names ethyl mesityl ketone oxime

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:153933-73-4 SDS

153933-73-4Downstream Products

153933-73-4Relevant academic research and scientific papers

The Reaction of Nitrile Oxide with Organometallic Compounds

Kim, Jae Nyoung,Kim, Hyoung Rae,Ryu, Eung K.

, p. 5117 - 5120 (1993)

Nitrile oxides react with some organometallic compounds with or without the aid of Lewis acid depending on the organometallic nucleophiles to give oxime derivatives in good yields.

Novel BODIPY preparations from sterically hindered pyrroles. Synthesis and photophysical behavior in solution, polystyrene nanoparticles, and solid phase

Meallet-Renault,Clavier,Dumas-Verdes,Badre,Shmidt, E. Yu.,Mikhaleva,Laprent,Pansu,Audebert,Trofimov

, p. 2247 - 2256 (2008)

Trimesityl-BODIPY (TMB), a new derivative of 4,4-difluoro-4-bora-3a,4a- diaza-s-indacene belonging to fluores-cent nanostructures series, was synthesized from the corresponding pyrrole by the Trofimov reaction. This reaction was also employed to obtain 2-[2.2]paracyclophanylpyrrole from 5-acetyl[2.2]-paracyclophane. The spectral properties of TMB have been investigated in dichloromethane, nanolatex (polystyrene) films prepared by rapid solvent evaporation, and microcrystals. Comparative analysis of TMB properties with those of mesityl-BODIPY (MB) was performed. TMB was prepared to minimize π-π interactions in order to preserve luminescence in the aggregate state. Both fluorophores were shown to form fluorescing aggregates in the amorphous state (film). Fluorescence spectra (extinction and lifetime) were also studied. In crystal, MB shows a weaker fluorescence, while TMB behaves as a single fluorescing aggregate with a lifetime of 9.5 ns.

Aluminium chloride promoted carbohydroximoylation reaction of aromatic compounds with primary nitroalkanes

Kim,Song,Ryu

, p. 1711 - 1715 (2007/10/02)

The reaction of primary nitroalkanes with aromatic compounds in the presence of aluminium chloride afforded the corresponding carbohydroximoylated aromatic compounds.

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