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N-(3,5-diacetamido-2-methyl-phenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55470-90-1

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55470-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55470-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,7 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55470-90:
(7*5)+(6*5)+(5*4)+(4*7)+(3*0)+(2*9)+(1*0)=131
131 % 10 = 1
So 55470-90-1 is a valid CAS Registry Number.

55470-90-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-Triacetaminotoluol

1.2 Other means of identification

Product number -
Other names N,N',N"-Tris(carboxyethyl)-1,4,7-triazacyclononane

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:55470-90-1 SDS

55470-90-1Relevant academic research and scientific papers

Triamidotoluene nucleating agent, preparation method and method of use

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Paragraph 0085-0086; 0088-0093, (2022/01/10)

The present invention provides a triamidotoluene nucleating agent, preparation method and method of use. Among them, triamidotoluene nucleating agent, is an N,N,N-triacyl-2,4,6-triaminotoluene compound, which can be used as a nucleating agent for polymer

Novel preparation method of insensitive explosive TATB

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Paragraph 0097-0102; 0111-0115; 0125-0129; 0138-0142, (2020/12/10)

The invention provides a novel preparation method of an insensitive explosive TATB. The method comprises the following steps: 1, with 2,4,6-trinitrotoluene as a raw material, subjecting 2,4,6-trinitrotoluene to reacting with hydrogen and acetic anhydride in sequence to obtain 2,4,6-triacetylaminotoluene; 2, subjecting the obtained 2,4,6-triacetylaminotoluene o oxidation and a decarboxylation reaction to obtain 1,3,5-triacetylaminobenzene; and 3, carrying out nitrification and hydrolysis reactions on the obtained 1,3,5-triacetylaminobenzene to obtain 2,4,6-trinitro-1,3,5-triaminobenzene. According to the invention, the raw material used in the preparation method is the cheap 2,4,6-trinitrotoluene, and used reactants or catalysts are commonly used products in the chemical industry, so the preparation method has characteristics of low cost and usage of simple and easily available raw materials. In addition, the preparation method also has the characteristics of short synthesis steps, simple operation of each step, high yield, high reaction rate, easy separation and collection of intermediate and final products and the like, and is beneficial for realization of mass production of TATB.

A novel kind of configurational dissymmetry. Preparation, resolution, and circular dichroism of cis-bis(1(a)-methyl-2(a),4(a),6(a)-triaminocyclohexane)cobalt(III) ion

Freeman, Wade A.,Liu, Chui Fan

, p. 2120 - 2124 (2007/10/16)

The ligand 1-methyl-2,4,6-triaminocyclohexane (Metach) has been prepared by a two-step catalytic reduction of 2,4,6-trinitrotoluene. The isomer isolated has all equatorial substituents on the cyclohexane ring. The bis cobalt(III) complex has been prepared and resolved with d-bromocamphorsulfonate. The visible-ultraviolet circular dichroism spectrum of the resolved ion has a single gaussian extremum of low magnitude. The enantiomer isolated is tentatively assigned the Λ absolute configuration on the basis of sector rule arguments.

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