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3698-54-2

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3698-54-2 Usage

Uses

Manufacture of detonators and primers.

Check Digit Verification of cas no

The CAS Registry Mumber 3698-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3698-54:
(6*3)+(5*6)+(4*9)+(3*8)+(2*5)+(1*4)=122
122 % 10 = 2
So 3698-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H3N5O8/c7-4-2(8(12)13)1-3(9(14)15)5(10(16)17)6(4)11(18)19/h1H,7H2

3698-54-2SDS

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 2,3,4,6-Tetranitroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,2,3,4,6-tetranitro

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:3698-54-2 SDS

3698-54-2Relevant articles and documents

Synthesis, Characterization, and Properties of Pentanitrobenzene C6H(NO2)5

Huber, Tanja,von der Heide, Chantal,Klap?tke, Thomas M.,Krumm, Burkhard

, p. 126 - 132 (2019/01/04)

The synthesis of the polynitroaromatic compound pentanitrobenzene was re-examined by modern spectroscopic, structural and physicochemical methods. Originally prepared in 1979, this material could exhibit interesting properties as an oxygen-rich energetic building block. The energies of formation were calculated with the GAUSSIAN program package and the detonation parameters were predicted using the EXPLO5 computer code. The performance data were determined and compared to the common oxidizer ammonium perchlorate. The crystal structure of pentanitrobenzene was determined by X-ray crystallography, and those of 2,3,4,6-tetranitroaniline and styphnic acid (trinitroresorcinol) were re-determined.

Synthesis of Polynitrodiazophenols

Atkins, Ronald L.,Wilson, William S.

, p. 2572 - 2578 (2007/10/02)

The formation of diazophenols by nitration of suitably substituted anilines and rearrangement of the nitroaromatic nitramines so formed is presented.The scope of the reaction is discussed, and a mechanism for the nitramine/diazophenol rearrangement is proposed which is consistent with 15N-labeling experiments.

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