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Acetamide, N,N'-(2,4,6-trinitro-1,3-phenylene)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88106-06-3

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88106-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88106-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,0 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88106-06:
(7*8)+(6*8)+(5*1)+(4*0)+(3*6)+(2*0)+(1*6)=133
133 % 10 = 3
So 88106-06-3 is a valid CAS Registry Number.

88106-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-acetamido-2,4,6-trinitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names N,N'-Diacetyl-2,4-diamino-1,3,5-trinitrobenzene

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:88106-06-3 SDS

88106-06-3Relevant academic research and scientific papers

Synthesis and purification of 1,3,5-triamino-2,4,6-trinitrobenzene (TATB)

-

Page/Page column 6, (2008/06/13)

A method to convert surplus nitroarene explosives (picric acid, ammonium picrate,) into TATB is described. The process comprises three major steps: conversion of picric acid/ammonium picrate into picramide; conversion of picramide to TATB through vicarious nucleophilic substitution (VNS) of hydrogen chemistry; and purification of TATB.

Synthesis of Polynitrobenzenes. Oxidation of Polynitroanilines and Their N-Hydroxy, N-Methoxy, and N-Acetyl Derivatives

Atkins, Ronald L.,Nielsen, Arnold T.,Bergens, Cynthia,Wilson, William S.

, p. 503 - 507 (2007/10/02)

Nitro-substituted arylhydroxylamines and alkyloxyamines have been oxidized to polynitroaryl compounds by utilizing ozone.Polynitroanilines have been oxidized to polynitroaromatics by peroxydisulfuric acid generated in situ from SO3 and ozone.Thus N-hydroxy-2,4,6-trinitroaniline (1a) or N-methoxy-2,4,6-trinitroaniline (1b) was cleanly oxidized to 1,2,3,5-tetranitrobenzene (2) by reaction with ozone in methylene chloride.Weakly basic amines such as pentanitroaniline (10) can conveniently be oxidized to hexanitrobenzene (11) in high yields by simply dissolving the amine in oleum and introducing ozone.A variety of substituted arylamines have been oxidized to polynitroaromatic compounds by using these two oxidation techniques.

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