383-65-3

Basic information

• Product Name: N-Allyl-2,2,2-trifluoroacetamide
• Synonyms: N-ALLYL-2,2,2-TRIFLUOROACETAMIDE;N-Allyltrifluoroacetamide;2-trifluoroacetaMide;N-allyl-2;Acetamide,2,2,2-trifluoro-N-2-propen-1-yl-
• CAS NO: 383-65-3
• Molecular Formula: C₅H₆F₃NO
• Molecular Weight: 153.1
• Mol File: 383-65-3.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 139-140 °C
• Flash Point: 48 °C
• Appearance: /
• Density: 1.191
• Vapor Pressure: 2.93mmHg at 25°C
• Refractive Index: 1.369
• Storage Temp.: 2-8°C
• PKA: 11.10±0.46(Predicted)
• CAS DataBase Reference: N-Allyl-2,2,2-trifluoroacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Allyl-2,2,2-trifluoroacetamide(383-65-3)
• EPA Substance Registry System: N-Allyl-2,2,2-trifluoroacetamide(383-65-3)

Safety Data

• Hazardous Substances Data: 383-65-3(Hazardous Substances Data)

Usage

General Description

N-Allyl-2,2,2-trifluoroacetamide is a synthetic organic compound with the chemical formula C6H9F3NO. It is a colorless liquid with a pungent odor and is commonly used as an intermediate in the production of pharmaceuticals and agrochemicals. N-Allyl-2,2,2-trifluoroacetamide is highly reactive due to the allyl group, which makes it useful in various chemical reactions such as allylation and nucleophilic substitution. N-Allyl-2,2,2-trifluoroacetamide is also used as a building block in the synthesis of complex organic molecules and can serve as a versatile starting material for the preparation of different functionalized compounds. Its trifluoroacetamide moiety imparts unique chemical and physical properties, making it a valuable component in the field of organic chemistry.

InChI:InChI=1/C5H6F3NO/c1-2-3-9-4(10)5(6,7)8/h2H,1,3H2,(H,9,10)

Upstream product

• 107-11-9 1-amino-2-propene 
• 407-25-0 trifluoroacetic anhydride 
• 68602-57-3 trifluoroacetyl triflate 
• 383-63-1 ethyl trifluoroacetate, 
• 815-06-5 N-methyl-2,2,2-trifluoroacetamide 
• 75-89-8 2,2,2-trifluoroethanol 
• 354-58-5 1,1,1-Trichloro-2,2,2-trifluoroethane 
• 431-47-0 trifluoroacetic acid-methyl ester 
• 76-05-1 trifluoroacetic acid 
• 109317-75-1 4-trifluoroacetyl-2,3-dihydrofuran 

Downstream Products

• 25222-21-3 2,2,2-Trifluoro-N-(1,4,5,6,7,7-hexafluoro-bicyclo[2.2.1]hept-5-en-2-ylmethyl)-acetamide 
• 1334031-91-2 (E)-2,2,2-trifluoro-N-(3-(4-methoxyphenyl)allyl)acetamide 
• 1185180-07-7 (RS) (E) 2-trifluoroacetyl-1,2,3,4-tetrahydro-6,7-dimethoxy-1-[4',5'-dimethoxy-2'-(3-trifluoroacetyl-1-propenyl)phenyl]methylisoquinoline 
• 1222166-03-1 (E)-2,2,2-trifluoro-N-(3-(3-nitrophenyl)allyl)acetamide 
• 1215076-89-3 C₁₈H₂₂F₃NOS 
• 1215077-79-4 (E)-N-(3-(3-(butylsulfonyl)phenyl)allyl)-2,2,2-trifluoroacetamide 
• 1215077-11-4 (E)-N-(3-(3-(2-ethyl-2-hydroxybutylthio)phenyl)allyl)-2,2,2-trifluoroacetamide 
• 1215077-68-1 (E)-N-(3-(3-(butylthio)phenyl)allyl)-2,2,2-trifluoroacetamide 
• 1141779-47-6 C₁₈H₂₂F₃NO₃ 
• 7446-09-5 sulfur dioxide 
• 869222-68-4 N-((E)-3-(1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)allyl)-2,2,2-trifluoroacetamide 
• 115794-55-3 5-(3''-trifluoroacetamidoallyl)-2'-deoxyuridine 
• 462117-95-9 2-(2,6-Difluorophenyl)-4-(4-(5-(trifluoroacetamidomethyl)isoxazolin-3-yl) phenyl)oxazoline 
• 153391-89-0 tetrahydro-3-methylidene-1-(trifluoroacetyl)-4-vinylpyrrole 

Relevant articles and documents

Efficiency and stability of spectral sensitization of boron-doped-diamond electrodes through covalent anchoring of a donor-acceptor organic chromophore (P1)

A novel procedure is developed for chemical modification of H-terminated B-doped diamond surfaces with a donor-π-bridge-acceptor molecule (P1). A cathodic photocurrent near 1 μA cm-2 flows under 1 Sun (AM 1.5) illumination at the interface betw

Electrochemical approach to trifluoroacetamide synthesis from 1,1,1-trichloro-2,2,2-trifluoroethane (CFC-113a) catalyzed by B12complex

One-pot synthetic approach to produce trifluoroacetamide has been developed using an electrochemical method with the B12 complex as a catalyst under mild conditions, in open air at room temperature. Thirty examples of trifluoroacetamide were synthesized from 1,1,1-trichloro-2,2,2-trifluoroethane (CFC-113a) in moderate to good yields. This user-friendly strategy is compatible with a broad range of trifluoroacetamide syntheses.

Anion Receptor, Electrolyte Containing the Anion Receptor and Lithium Ion Battery and Lithium Ion Capacitor Using the Electrolyte

The present invention relates to a novel anion acceptor having a high cation transport rate and improved lifespan, an electrolyte containing the same, and a lithium ion battery and a lithium ion capacitor manufactured using the electrolyte and, more specifically, to a compound represented by chemical formula 1. In the chemical formula 1, n is an integer from 1 to 50, and X is one or more selected from the group consisting of -NR_1R_2, -NR_3R_4, -Ph(-(m)-R_5), and -O-(CH_2CH_2O)_y-CH_3.COPYRIGHT KIPO 2018