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ETHYL 4 4 4-TRIFLUORO-2-BUTYNOATE(CAS# 79424-03-6)

Chemical Property:

Molecular Formula C6H5F3O2
Molar Mass 166.1
Density 1.162g/mLat 25°C(lit.)
Boling Point 96-98°C(lit.)
Flash Point 43°F
Water Solubility Soluble in water (partly).
Solubility Chloroform (Slightly), Methanol (Slightly)
Appearance Liquid
Specific Gravity 1.162
Color Clear colorless
BRN 3539414
Storage Condition Inert atmosphere,2-8°C
Stability Volatile
Refractive Index n20/D 1.350(lit.)
Physical and Chemical Properties Specific gravity 1.162

Product Detail

Product Tags

Risk Codes R11 – Highly Flammable
R36/37/38 – Irritating to eyes, respiratory system and skin.
Safety Description S16 – Keep away from sources of ignition.
S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 – Wear suitable protective clothing, gloves and eye/face protection.
UN IDs UN 3272 3/PG 2
WGK Germany 3
FLUKA BRAND F CODES 19
HS Code 29161900
Hazard Note Irritant/Highly Flammable
Hazard Class 3.1
Packing Group II

 

Introduction

ETHYL 4,4,4-TRIFLUORO-2-BUTYNOATE(ETHYL 4,4,4-TRIFLUORO-2-BUTYNOATE) is an organic compound. The following is a description of its nature, use, preparation and safety information:

 

Nature:

-Appearance: It is usually a colorless liquid or yellowish liquid.

-Solubility: It can be dissolved in organic solvents, such as ethanol, ether and dichloromethane.

-Melting point and boiling point: Its melting point is about -8°C, and its boiling point is about 108-110°C.

 

Use:

-reagent in Advanced Organic Synthesis: ETHYL 4,4, 4-trifluororo-2-butynoate can be used as an important reagent in organic synthesis. It can participate in a variety of organic reactions, such as acylation, condensation and cyclization reactions, used to synthesize a variety of organic compounds.

-Material chemistry: It can also be used for certain reactions in polymer chemistry, such as crosslinking agents for synthetic polymers.

 

Method:

ETHYL 4,4,4-TRIFLUORO-2-BUTYNOATE can be prepared by the following steps:

1. First, butynol (2-butynol) is reacted with anhydrous hydrogen fluoride to generate butynyl fluoride.

2. Then, the butynyl fluoride is reacted with ETHYL chloroacetate to generate ETHYL 4,4, 4-trifluororo-2-butynoate.

 

Safety Information:

- ETHYL 4,4,4-TRIFLUORO-2-BUTYNOATE should avoid prolonged exposure to the air because it is sensitive to moisture and water.

-It should avoid open flames and high temperatures during operation and storage, because it is flammable.

-Appropriate protective measures should be taken when using and handling it, including wearing gloves, masks and protective glasses.

-It should be stored in a cool, dry and well-ventilated place.


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