ChemicalBook > CAS DataBase List > 2-[3-(Trifluoromethyl)benzoyl]aminoacetic acid

2-[3-(Trifluoromethyl)benzoyl]aminoacetic acid

Product Name
2-[3-(Trifluoromethyl)benzoyl]aminoacetic acid
CAS No.
17794-48-8
Chemical Name
2-[3-(Trifluoromethyl)benzoyl]aminoacetic acid
Synonyms
EOS-61907;2-acetic acid;3-trifluoromethylhippurate;m-Trifluoromethylhippuric acid;(3-(trifluoromethyl)benzoyl)glycine;N-(3-(TRIFLUOROMETHYL)BENZOYL)GLYCINE;Glycine, N-[3-(trifluoromethyl)benzoyl]-;2-{[(3-trifluoromethyl)benzoyl]amino}acetic;2-(3-(TRIFLUOROMETHYL)BENZAMIDO)ACETIC ACID;([3-(TRIFLUOROMETHYL)BENZOYL]AMINO)ACETIC ACID
CBNumber
CB2258508
Molecular Formula
C10H8F3NO3
Formula Weight
247.17
MOL File
17794-48-8.mol
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2-[3-(Trifluoromethyl)benzoyl]aminoacetic acid Property

Melting point:
134-138°C
Boiling point:
401.7±45.0 °C(Predicted)
Density 
1.417±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
3.69±0.10(Predicted)
Appearance
White to light yellow Solid
CAS DataBase Reference
17794-48-8(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2924297099
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

Precautionary statements

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
T790853
Product name
2-(3-(Trifluoromethyl)benzamido)aceticAcid
Packaging
50mg
Price
$45
Updated
2021/12/16
AK Scientific
Product number
W3882
Product name
2-{[3-Trifluoromethyl)benzoyl]amino}aceticacid
Packaging
5g
Price
$296
Updated
2021/12/16
ChemScene
Product number
CS-M0140
Product name
2-(3-(trifluoromethyl)benzamido)aceticacid
Packaging
5g
Price
$169
Updated
2021/12/16
ChemScene
Product number
CS-M0140
Product name
2-(3-(trifluoromethyl)benzamido)aceticacid
Packaging
10g
Price
$285
Updated
2021/12/16
Activate Scientific
Product number
AS92978
Product name
N-[3-(Trifluoromethyl)benzoyl]glycine
Purity
95+%
Packaging
5G
Price
$287
Updated
2021/12/16
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2-[3-(Trifluoromethyl)benzoyl]aminoacetic acid Chemical Properties,Usage,Production

Definition

ChEBI: M-Trifluoromethylhippuric acid is a N-acylglycine. It is functionally related to a N-benzoylglycine.

Synthesis

2251-65-2

56-40-6

17794-48-8

GENERAL STEPS: In a 12 L four-necked round-bottomed flask equipped with a thermocouple controller, mechanical stirrer, heating jacket, condenser tube, and nitrogen inlet and outlet fittings, glycine (1, Alfa Aesar) (318 g, 4.19 mol), acetonitrile (1.2 L), and sodium hydroxide solution (5.31 L, 10.62 mol) were added. The mixture was cooled with stirring to 4°C. A solution of 3-(trifluoromethyl)benzoyl chloride (2, Alfa Aesar) (885.0 g, 4.12 mol) dissolved in acetonitrile (0.75 L) was added slowly and dropwise over a period of 2 h (1.39 L in total) while the internal temperature was controlled to be between 4-6°C. The mixture was then purified with a mixture of 2.5 g, 4.12 mol and 3-(trifluoromethyl)benzoyl chloride (2, Alfa Aesar). The resulting slightly orange-pink colored solution was continued to be stirred at 4°C for 30 min. The reaction mixture was acidified to pH=3 with concentrated hydrochloric acid (400 mL of 37% HCl solution was added over 30 min, keeping the temperature between 0-6°C) and stirred at 0°C for 1 h until a slightly pale yellow suspension was formed. The solid was collected by filtration, washed with cold (0°C) deionized water (300 mL x 2), dried in air for 2 h, and placed in a 60°C drying oven. Drying under room vacuum (120 mmHg) for 20 h gave pure 2-(3-(trifluoromethyl)benzoylamino)acetic acid (3) as an off-white solid. The filtrate was extracted with ethyl acetate (1 L x 2), and the combined organic phases were washed with brine (300 mL), concentrated to 66°C at room temperature, and then concentrated under high vacuum (20 mmHg) to give the crude product as an off-white waxy solid. The crude product was ground, sonicated with toluene (1 L) and stirred at 10°C for 1 hour. The solid was collected by filtration, washed with hexane (50 mL x 2) and dried in a vacuum oven at 50°C to give additional pure 2-(3-(trifluoromethyl)benzoylamino)acetic acid (3) as an off-white solid. The structure of product 3 was confirmed by 1H-NMR.

References

[1] Patent: US2010/144695, 2010, A1. Location in patent: Page/Page column 61-62
[2] Patent: EP2452939, 2012, A2. Location in patent: Page/Page column 17
[3] Patent: US2012/190689, 2012, A1. Location in patent: Page/Page column 11-12
[4] Patent: US2005/192302, 2005, A1. Location in patent: Page/Page column 21
[5] Patent: WO2012/114223, 2012, A1. Location in patent: Page/Page column 36

2-[3-(Trifluoromethyl)benzoyl]aminoacetic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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17794-48-8, 2-[3-(Trifluoromethyl)benzoyl]aminoacetic acidRelated Search:


  • ([3-(TRIFLUOROMETHYL)BENZOYL]AMINO)ACETIC ACID
  • 2-([3-(TRIFLUOROMETHYL)BENZOYL]AMINO)ACETIC ACID
  • N-(3-(TRIFLUOROMETHYL)BENZOYL)GLYCINE
  • 2-acetic acid
  • 2-(3-(TRIFLUOROMETHYL)BENZAMIDO)ACETIC ACID
  • 3-trifluoromethylhippurate
  • m-Trifluoromethylhippuric acid
  • 2-{[(3-trifluoromethyl)benzoyl]amino}acetic
  • Glycine, N-[3-(trifluoromethyl)benzoyl]-
  • EOS-61907
  • 2-[3-(Trifluoromethyl)benzoyl]aminoacetic acid-4
  • (3-(trifluoromethyl)benzoyl)glycine
  • 2-(3-(trifluoromethyl)benzamido)acetic acid, CAS 17794-48-8
  • 17794-48-8
  • C10H8F3NO3
  • ARYL AMIDE
  • Phenyls & Phenyl-Het
  • Aromatic Halides (substituted)
  • Phenyls & Phenyl-Het