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Morpholine, 2,2,6-trifluoro-4-methyl-, is an organic compound characterized by a morpholine ring with a trifluoromethyl group at the 4 position. This unique structure endows it with enhanced chemical and physical properties, including stability and resistance to degradation. The trifluoromethyl substitution also imparts valuable characteristics, making it a versatile chemical with a range of applications across different industries.

80958-33-4

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80958-33-4 Usage

Uses

Used in Chemical Processes:
Morpholine, 2,2,6-trifluoro-4-methylis utilized as a solvent in various chemical processes due to its ability to dissolve a wide range of substances and facilitate reactions.
Used as a Corrosion Inhibitor:
Morpholine, 2,2,6-trifluoro-4-methylserves as an effective corrosion inhibitor, protecting materials from degradation in harsh environments, which is crucial in industries such as oil and gas, where equipment is often exposed to corrosive conditions.
Used as a Catalyst:
In catalytic processes, Morpholine, 2,2,6-trifluoro-4-methylacts to accelerate chemical reactions, improving efficiency and reducing the need for harsh conditions or excessive amounts of reactants.
Used in Pharmaceutical Synthesis:
As an intermediate in the synthesis of pharmaceuticals, Morpholine, 2,2,6-trifluoro-4-methyl- contributes to the development of new drugs, leveraging its unique properties to create molecules with specific therapeutic effects.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, Morpholine, 2,2,6-trifluoro-4-methylis employed as an intermediate to produce compounds that can enhance crop protection and yield.
Used as a Ligand in Metal-Catalyzed Reactions:
Morpholine, 2,2,6-trifluoro-4-methyl-'s ability to act as a ligand in metal-catalyzed reactions makes it instrumental in the synthesis of complex organic molecules, which are often required in advanced materials and specialty chemicals.
Its low toxicity and minimal environmental impact make Morpholine, 2,2,6-trifluoro-4-methyl-, a preferred choice in applications where safety and sustainability are paramount.

Check Digit Verification of cas no

The CAS Registry Mumber 80958-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,5 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80958-33:
(7*8)+(6*0)+(5*9)+(4*5)+(3*8)+(2*3)+(1*3)=154
154 % 10 = 4
So 80958-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H8F3NO/c1-9-2-4(6)10-5(7,8)3-9/h4H,2-3H2,1H3

80958-33-4SDS

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 2,2,6-trifluoro-4-methylmorpholine

1.2 Other means of identification

Product number -
Other names 2,2,6-trifluoro-4-methyl-morpholine

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:80958-33-4 SDS

80958-33-4Upstream product

80958-33-4Downstream Products

80958-33-4Relevant academic research and scientific papers

THE ELECTROCHEMICAL FLUORINATION OF ORGANIC COMPOUNDS: FURTHER DATA IN SUPPORT OF THE ECbECN MECHANISM

Gambaretto, G. P.,Napoli, M.,Conte, L.,Scipioni, A.,Armelli, R.

, p. 149 - 156 (2007/10/02)

Data in support of the four-stage mechanism ECbECN result from the electrochemical fluorination of some acyl halides (benzoyl, n-butyryl and iso-butyryl, benzenesulphonyl and p-toluenesulphonyl chlorides) and amines (tripropylamine and N-methylmorpholine).

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