1171331-39-7

Basic information

• Product Name: 2-AMino-N-(2,2,2-trifluoroethyl)acetaMide hydrochloride
• Synonyms: 2-AMino-N-(2,2,2-trifluoroethyl)acetaMide hydrochloride
• CAS NO: 1171331-39-7
• Molecular Formula: C₄H₇F₃N₂O*ClH
• Molecular Weight: 192.5673296
• Product Categories: Intermediates
• Mol File: 1171331-39-7.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 2-AMino-N-(2,2,2-trifluoroethyl)acetaMide hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMino-N-(2,2,2-trifluoroethyl)acetaMide hydrochloride(1171331-39-7)
• EPA Substance Registry System: 2-AMino-N-(2,2,2-trifluoroethyl)acetaMide hydrochloride(1171331-39-7)

Safety Data

• Hazardous Substances Data: 1171331-39-7(Hazardous Substances Data)

Usage

Uses

Reactant in the synthesis of isoxazoline indolizine amides.

Upstream product

• 359821-38-8 2-ammonia-N-(2,2,2-trifluoroethyl)acetamide 
• 1371632-79-9 phenylmethyl N-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]carbamate 
• 1371632-80-2 2-[bis(phenylmethyl)amino]-N-(2,2,2-trifluoroethyl)acetamide 
• 1231755-15-9 2-N-(tert-butoxycarbonyl)-1-oxo-1-N-(2,2,2-trifluoroethyl)-1,2-diaminoethane 

Downstream Products

• 1233232-77-3 2-({2-chloro-4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-N-hydroxy-benzimidoyl}-amino)-N-(2,2,2-trifluoro-ethyl)-acetamide 
• 864731-61-3 A₁₄₄₃ 
• 1369852-71-0 (S)-5-[5-(3,4,5-trichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-3-methyl-thiophene-2-carboxylic acid [(2,2,2-trifluoro-ethylcarbamoyl)-methyl]-amide 
• 1093861-60-9 4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]-1-naphthalenecarboxamide 
• 1122022-02-9 A664 
• 1312697-19-0 5-(5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-N-(2-oxo-2-(2,2,2-trifluoroethylamino)ethyl)indolizine-8-carboxamide 
• 1444176-77-5 4-[5-(3,5-dichlorophenyl)-4-fluoro-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-N-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]benzamide 
• 1427273-67-3 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isothiazol-3-yl]-2-methyl-N-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]benzamide 

Relevant articles and documents

PROCESS FOR THE PREPARATION OF 2-AMINO-N-(2,2,2-TRIFLUOROETHYL)-ACETAMIDE AND SALTS THEREOF

The present invention relates to an improved process for the preparation of 2-amino-N-(2,2,2-trifluoroethyl) acetamide of formula (I) and salts (IA) thereof, in an environment friendly and commercially viable manner in high yield and greater chemical purity.

MOLECULES HAVEING PESTICIDAL UTILIY AND INTERMEDIATES, COMPOSITIONS AND PROCESSES RELATED THERETO

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and processes of using such pesticidal compositions against such pests. These pesticidal compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).

2-amino-N-(2, 2, 2-trifluoroethyl) or its salt aminoacetamide compd.

PROBLEM TO BE SOLVED: To provide a method for producing a substituted 2-amino-N-(2,2,2-trifluoroethyl)acetamide or a salt thereof. SOLUTION: The method for producing 2-amino-N-(2,2,2-trifluoroethyl)acetamide or a salt thereof comprises, as shown in chemical reaction formula (A), reaction of 2,2,2-trifluoroethylamine or a salt thereof with an acyl compound preferably in the presence of water and an inorganic base, and through this compound, the objective 2-amino-N-(2,2,2-trifluoroethyl)acetamide or a salt thereof is obtained. COPYRIGHT: (C)2009,JPO&INPIT

NOVEL ISOXAZOLINES AND THEIR USE IN CONTROLLING PESTS

Disclosed herein are novel isoxazoline compounds of the general formula (I), compositions comprising these novel compounds, and uses of these compounds in the control of pests in both animal health and plant protection contexts. The compounds can be combined with other biologically active materials such as organophosphate pesticides, carbamate -type pesticides, organochlorine type pesticides, pyrethrins/pyrethroids, neonicotinoids, avermectins, milbemycins, benzimidazoles, salicylanilides, substituted phenols, pyrimidines, tetrahydropyrimidines, imidazothiazoles, amino/amido acetonitrile derivatives, febantel, clorsulon, levamisole, morantel, and praziquantel, juvenile hormone mimics and chitin synthesis inhibitors. (I)

METHOD FOR PREPARING 2-AMINO-N-(2,2,2-TRIFLUOROETHYL) ACETAMIDE

Disclosed are methods for preparing compounds of Formula 1 and 1A. The first method utilizes a benzyl carbamate amine protecting group and an intermediate of Formula 4. The second method utilizes a tert-butyl carbamate amine protecting group and an interm