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2-[(aminooxy)sulfonyl]-1,3,5-tri(propan-2-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38202-21-0

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38202-21-0 Usage

Structure

A derivative of benzene with three propan-2-yl groups attached to the benzene ring and a sulfonyl group connected to an aminooxy moiety.

Usage

Commonly used as a reagent in organic synthesis, particularly in the formation of oxime esters.

Therapeutic potential

Has been studied for its potential use as a therapeutic agent due to its ability to inhibit the activity of specific enzymes involved in disease processes.

Other potential uses

Has been investigated for its potential use as a herbicide and as a crosslinking agent for polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 38202-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,0 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38202-21:
(7*3)+(6*8)+(5*2)+(4*0)+(3*2)+(2*2)+(1*1)=90
90 % 10 = 0
So 38202-21-0 is a valid CAS Registry Number.

38202-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name amino 2,4,6-tri(propan-2-yl)benzenesulfonate

1.2 Other means of identification

Product number -
Other names -

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:38202-21-0 SDS

38202-21-0Downstream Products

38202-21-0Relevant academic research and scientific papers

Novel catenated N6 energetic compounds based on substituted 1,2,4-triazoles: Synthesis, structures and properties

Li, Yanan,Wang, Bin,Chang, Pei,Hu, Jianjian,Chen, Tao,Wang, Yinglei,Wang, Bozhou

, p. 13755 - 13763 (2018/04/25)

1-Amino-3,5-dinitro-1,2,4-triazole (ADNT) was prepared using an efficient N-amination process. Three novel catenated N6 energetic derivatives of ADNT, which contain 1,1′-azobis(3,5-dinitro-1,2,4-triazole) (ABDNT), 1,1′-azobis(3-chloro-5-nitro-1,2,4-triazole) (ABCNT) and 1,1′-azobis(3,5-diazido-1,2,4-triazole) (ABDAT), were synthesized from N-amino oxidative-coupling reactions of ADNT. All compounds were fully characterized by 1H and 13C nuclear magnetic resonance spectroscopies, infrared spectroscopy, elemental analysis, mass spectrum, as well as differential scanning calorimetry (DSC). The crystal structure of compound ABCNT was confirmed by single-crystal X-ray diffraction showing an extensive conjugated structure. The densities of energetic derivatives ranged from 1.71 to 1.93 g cm-3, and all compounds have positive heats of formation in the range of 774.8 to 2150.8 kJ mol-1. Based on the measured densities and calculated heats of formation, theoretical performance calculations, including detonation pressures (29.6-42.4 GPa) and detonation velocities (8.22-9.49 km s-1) were carried out using the Gaussian 09 program and Kamlet-Jacobs equations, and they compared favorably with those of TNT and RDX. These properties make them potentially competitive as new high energy-density compounds.

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