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2,4,6-tris(2-chloropropan-2-yl)-1,3,5-trioxane is a chemical compound with the molecular formula C15H21Cl3O3. It is a white, crystalline solid that is used as a chemical intermediate and a building block in the synthesis of various organic compounds. This trisubstituted trioxane features three 2-chloropropan-2-yl groups attached to a 1,3,5-trioxane ring, and has been studied for its potential applications in materials science, pharmaceuticals, and agrochemicals. It also exhibits some insecticidal properties, although further research is needed to understand its exact mode of action and potential uses in this area.

7471-98-9

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7471-98-9 Usage

Uses

Used in Chemical Synthesis:
2,4,6-tris(2-chloropropan-2-yl)-1,3,5-trioxane is used as a chemical intermediate for the synthesis of various organic compounds, contributing to the development of new materials and products in different industries.
Used in Materials Science:
In the field of materials science, 2,4,6-tris(2-chloropropan-2-yl)-1,3,5-trioxane is used as a building block to create novel materials with specific properties, such as improved stability or reactivity.
Used in Pharmaceuticals:
2,4,6-tris(2-chloropropan-2-yl)-1,3,5-trioxane is utilized as a component in the development of pharmaceuticals, potentially leading to new drug formulations and treatments.
Used in Agrochemicals:
2,4,6-tris(2-chloropropan-2-yl)-1,3,5-trioxane is also used in agrochemicals, where it may contribute to the creation of new pesticides or other agricultural products to improve crop protection and yield.
Used in Insecticides:
2,4,6-tris(2-chloropropan-2-yl)-1,3,5-trioxane has been found to possess insecticidal properties, and it is used as a potential active ingredient in the development of new insecticides. However, its exact mode of action and full potential in this area are still under investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 7471-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7471-98:
(6*7)+(5*4)+(4*7)+(3*1)+(2*9)+(1*8)=119
119 % 10 = 9
So 7471-98-9 is a valid CAS Registry Number.

7471-98-9SDS

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 2,4,6-tris(2-chloropropan-2-yl)-1,3,5-trioxane

1.2 Other means of identification

Product number -
Other names 2,4,6-tris-(1-chloro-1-methyl-ethyl)-[1,3,5]trioxane

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:7471-98-9 SDS

7471-98-9Upstream product

7471-98-9Downstream Products

7471-98-9Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF 2,2-DIMETHYLPIPERAZINE

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Page/Page column 12, (2019/10/29)

This invention relates to a novel chemical process for the synthesis of 2,2-dimethylpiperazine and the further transformation of 2,2-dimethylpiperazine into ferf-butyl-3,3-dimethylpiperazine-l- carboxylate-hemi-DL-tartrate.

Synthesis and low temperature spectroscopic observation of 1,3,5-trioxane-2,4,6-trione: The cyclic trimer of carbon dioxide

Rodig, Michael J.,Snow, Arthur W.,Scholl, Paul,Rea, Simon

, p. 5354 - 5361 (2016/07/13)

1,3,5-Trioxane-2,4,6-trione (cyclic trimer of CO2) is the product of a four-step synthesis: chlorination of isobutyraldehyde; cyclotrimerization of 2-chloro-2-methylpropanal; dehydochlorination of 2,4,6-tris(2-chloropropan)-2-yl-1,3,5-trioxane; ozonolysis at -80 °C of 2,4,6-tri(propan-2-ylidene)-1,3,5-trioxane. This trioxane-trione is detected in solution at temperatures between -80 to -40 °C, and its conversion to CO2 is monitored by 13C NMR and FTIR. The CO2 trimer has a half-life of approximately 40 min at -40 °C.

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