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Methyl 4-amino-3-(trifluoromethoxy)benzoate

CAS No.
457097-93-7
Chemical Name:
Methyl 4-amino-3-(trifluoromethoxy)benzoate
Synonyms
Methyl 4-amino-3-(trifluoromethoxy)benzoate;3-trifluoromethoxy-4-aminobenzoate methyl ester;Benzoic acid, 4-amino-3-(trifluoromethoxy)-, methyl ester
CBNumber:
CB12688652
Molecular Formula:
C9H8F3NO3
Molecular Weight:
235.16
MDL Number:
MFCD15527567
MOL File:
457097-93-7.mol
MSDS File:
SDS
Last updated:2026-05-27 23:27:41

Methyl 4-amino-3-(trifluoromethoxy)benzoate Properties

storage temp. Keep in dark place,Inert atmosphere,Room temperature
Appearance Yellow to brown Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P280-P305+P351+P338
HS Code  2918290090

Methyl 4-amino-3-(trifluoromethoxy)benzoate price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth HTA09793 Methyl 4-amino-3-(trifluoromethoxy)benzoate 457097-93-7 2.5g $354 2026-06-04 Buy
Apolloscientific PC53602 Methyl 4-amino-3-(trifluoromethoxy)benzoate 95% 457097-93-7 250mg $25 2026-06-04 Buy
Apolloscientific PC53602 Methyl 4-amino-3-(trifluoromethoxy)benzoate 95% 457097-93-7 1g $32 2026-06-04 Buy
Apolloscientific PC53602 Methyl 4-amino-3-(trifluoromethoxy)benzoate 95% 457097-93-7 5g $98 2026-06-04 Buy
Apolloscientific PC53602 Methyl 4-amino-3-(trifluoromethoxy)benzoate 95% 457097-93-7 10g $160 2026-06-04 Buy
Product number Packaging Price Buy
HTA09793 2.5g $354 Buy
PC53602 250mg $25 Buy
PC53602 1g $32 Buy
PC53602 5g $98 Buy
PC53602 10g $160 Buy

Methyl 4-amino-3-(trifluoromethoxy)benzoate Chemical Properties,Uses,Production

Synthesis

4-Amino-3-(trifluoromethoxy)benzoic acid

175278-22-5

Methanol

67-56-1

Methyl 4-amino-3-(trifluoromethoxy)benzoate

457097-93-7

Thionyl chloride (2.68 g, 0.023 mol) was slowly added dropwise to methanol (12 mL) via a syringe at -5 °C, ensuring that the reaction temperature did not exceed -4 °C. After the dropwise addition was completed, the reaction mixture was stirred continuously at -5 °C or lower for 1 hour. Subsequently, 4-amino-3-(trifluoromethoxy)benzoic acid (0.5 g, 0.003 mol) [Alfa Aesar] was added all at once. The reaction mixture was transferred to ambient temperature and stirred for 3 days. After completion of the reaction, the solvent was removed by vacuum concentration. Water (10 mL) was added to the residue and sodium bicarbonate (0.46 g, 5.4 mmol) was added all at once and stirred at ambient temperature for 30 min. The mixture was extracted several times using ethyl acetate. The organic phases were combined, dried with sodium sulfate, filtered and concentrated in vacuum to afford methyl 4-amino-3-(trifluoromethoxy)benzoate 1.02 g (96.2% yield), which was initially a reddish oily material, and gradually transformed to a brown solid after cooling. Mass Spectrometry (MS): m/z 236.1 (MH+). 1H NMR (500MHz, DMSO-d6) data: δ3.771 (s, 3H), 6.329 (s, 2H), 6.834 (d, 1H), 7.6181 (s, 1H), 7.655 (dd, 1H).

References

[1] Patent: WO2014/165816, 2014, A1. Location in patent: Page/Page column 92
[2] Patent: US2015/175557, 2015, A1. Location in patent: Paragraph 0300
[3] Patent: EP2017263, 2009, A1. Location in patent: Page/Page column 213
[4] Patent: US2013/115194, 2013, A1. Location in patent: Paragraph 0335
[5] Patent: US2013/287731, 2013, A1. Location in patent: Paragraph 0284; 0285

Methyl 4-amino-3-(trifluoromethoxy)benzoate Preparation Products And Raw materials

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Methyl 4-amino-3-(trifluoromethoxy)benzoate Spectrum

Methyl 4-amino-3-(trifluoromethoxy)benzoate Benzoic acid, 4-amino-3-(trifluoromethoxy)-, methyl ester 3-trifluoromethoxy-4-aminobenzoate methyl ester 457097-93-7