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1,3,5,7-tetrakis[(trifluoromethyl)sulfanyl]-1,3,5,7-tetrazocane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81267-91-6

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81267-91-6 Usage

Structure

Tetrazocane derivative with four trifluoromethylsulfanyl groups attached to the nitrogen atoms

Type of compound

Highly sensitive explosive

Applications

Potential use in the field of energetic materials, military and industrial applications

Energy density

High

Sensitivity

Extreme sensitivity and potential for detonation

Safety

Challenging to handle and store safely, strict safety protocols required when working with it

Check Digit Verification of cas no

The CAS Registry Mumber 81267-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,6 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81267-91:
(7*8)+(6*1)+(5*2)+(4*6)+(3*7)+(2*9)+(1*1)=136
136 % 10 = 6
So 81267-91-6 is a valid CAS Registry Number.

81267-91-6SDS

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 1,3,5,7-tetrakis(trifluoromethylsulfanyl)-1,3,5,7-tetrazocane

1.2 Other means of identification

Product number -
Other names Octahydro-1,3,5,7-tetrakis(trifluormethylthio)-1,3,5,7-tetrazocin

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:81267-91-6 SDS

81267-91-6Downstream Products

81267-91-6Relevant academic research and scientific papers

Chemistry of Trifluoromethyl-Sulfur-Nitrogen Compounds, XI. Reactions of (CFnCl3-nS)xNH3-x with Selected Aldehydes

Borowski, Herbert E.,Haas, Alois

, p. 523 - 532 (2007/10/02)

CF3SNH2 and CF2ClSNH2 react with formaldehyde to yield (RNCH2)n (n = 3, 4, 5, R = SCF3 2c, d, e; n = 3, 4, R = SCF2Cl 2a, b), (2f), (2g), (2h), and CF2ClSN(CH3)CH2N(CH3)SCF2Cl (3), respectively, and with benzaldehyde to give C6H5CH=NR (R = SCF3 1b, SCF2Cl 1a). (CF3S)2NH reacts with formaldehyde under various conditions to yield (CF3S)2NCH2OH (4), (CF3S)2NxCH2N(SCF3)2 (x = 0 - 5, 5a - f), (CF3S)2NmCH2N(SCF3)2 (m = 1, 2, 6a, b), and (CF3SNH2)3 (2c).In the reaction of the less reactive (CF2ClS)2NH with formaldehyde (CF3ClS)2NnCH2N(SCF2Cl)2 (n = 1, 2, 8a, b) are obtained.The base adduct (CF3S)2NH.N(CH3)3 decomposes thermally to yield (CF3S)2NCH2N(H)SCF3 (7) and 5a.A reaction path is proposed.IR-, 1H-, 13C-, 19F NMR data well as mass spectra are presented.

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