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2-Methoxy-5-(trifluoromethoxy)benzaldehyde

CAS No.
145742-65-0
Chemical Name:
2-Methoxy-5-(trifluoromethoxy)benzaldehyde
Synonyms
2-Formyl-4-(trifluoromethoxy)anisole;2-Methoxy-5-(trifluoromethoxy)benzaldehyde;Benzaldehyde, 2-methoxy-5-(trifluoromethoxy)-;2-Methoxy-5-(trifluoromethoxy)benzaldehyde>2-Formyl-4-(trifluoromethoxy)anisole, 3-Formyl-4-methoxy-alpha,alpha,alpha-trifluoroanisole
CBNumber:
CB8104801
Molecular Formula:
C9H7F3O3
Molecular Weight:
220.15
MDL Number:
MFCD04115958
MOL File:
145742-65-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:55:10

2-Methoxy-5-(trifluoromethoxy)benzaldehyde Properties

Melting point 20-25℃
Boiling point 247.9±35.0 °C(Predicted)
Density 1.36
refractive index 1.475
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form clear liquid
color Light orange to Yellow to Green
Sensitive Air Sensitive
CAS DataBase Reference 145742-65-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P280a-P305+P351+P338-P321-P332+P313-P337+P313-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi
Hazard Note  Irritant
HS Code  2913000090
NFPA 704
1
2 0

2-Methoxy-5-(trifluoromethoxy)benzaldehyde price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical M1945 2-Methoxy-5-(trifluoromethoxy)benzaldehyde >98.0%(GC) 145742-65-0 5g $70 2026-04-30 Buy
TCI Chemical M1945 2-Methoxy-5-(trifluoromethoxy)benzaldehyde >98.0%(GC) 145742-65-0 25g $271 2021-12-16 Buy
Biosynth FM70452 2-Methoxy-5-(trifluoromethoxy)benzaldehyde 145742-65-0 25g $181.5 2026-06-04 Buy
Biosynth FM70452 2-Methoxy-5-(trifluoromethoxy)benzaldehyde 145742-65-0 50g $354 2026-06-04 Buy
Biosynth FM70452 2-Methoxy-5-(trifluoromethoxy)benzaldehyde 145742-65-0 100g $680 2026-06-04 Buy
Product number Packaging Price Buy
M1945 5g $70 Buy
M1945 25g $271 Buy
FM70452 25g $181.5 Buy
FM70452 50g $354 Buy
FM70452 100g $680 Buy

2-Methoxy-5-(trifluoromethoxy)benzaldehyde Chemical Properties, Uses, Production

Synthesis

2-HYDROXY-5-(TRIFLUOROMETHOXY)BENZALDEHYDE

93249-62-8

Iodomethane

74-88-4

2-METHOXY-5-(TRIFLUOROMETHOXY)BENZALDEHYDE

145742-65-0

(Step 1) To a 25 mL round-bottomed flask was added 1.0 g (4.85 mmol) of 5-(trifluoromethoxy)salicylaldehyde, 8 mL of dimethylformamide (DMF), and 738 mg (5.34 mmol) of potassium carbonate, and the mixture was stirred at room temperature for 30 min. Subsequently, 758 mg (5.34 mmol) of iodomethane dissolved in 2 mL of DMF was slowly added dropwise to the reaction system under ice bath cooling conditions. After the dropwise addition, stirring was continued under ice bath conditions for 1 h. The ice bath was then withdrawn and the reaction mixture was allowed to stir for 19 h at room temperature. Upon completion of the reaction, 20 mL of ethyl acetate and 20 mL of water were added to the mixture and the organic layer was separated by shaking thoroughly. The aqueous layer was extracted again with 20 mL of ethyl acetate and all organic layers were combined. The organic phase was sequentially washed twice with 20 mL of water and then twice with 20 mL of saturated saline. Finally, the organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 1.0 g of 2-methoxy-5-(trifluoromethoxy)benzaldehyde in 93% yield. The product was characterized by 1H-NMR (CDCl3): δ 3.96 (s, 3H), 7.02 (d, 1H, J = 8.8 Hz), 7.41 (d, 1H, J = 9.2 Hz), 7.69 (s, 1H), 10.44 (s, 1H).

References

[1] Patent: EP1460062, 2004, A1. Location in patent: Page 70

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2-Formyl-4-(trifluoromethoxy)anisole 2-Formyl-4-(trifluoromethoxy)anisole, 3-Formyl-4-methoxy-alpha,alpha,alpha-trifluoroanisole 2-Methoxy-5-(trifluoromethoxy)benzaldehyde> Benzaldehyde, 2-methoxy-5-(trifluoromethoxy)- 2-Methoxy-5-(trifluoromethoxy)benzaldehyde 145742-65-0 Fluorine series Aromatic Aldehydes & Derivatives (substituted) Adehydes, Acetals & Ketones Anisoles, Alkyloxy Compounds & Phenylacetates Fluorine Compounds