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(4-Methoxybenzyloxy)acetic acid

CAS No.
88920-24-5
Chemical Name:
(4-Methoxybenzyloxy)acetic acid
Synonyms
p-methoxybenzyloxy acetic acid;2-((4-Methoxybenzyl)oxy)acetic acid;(4-METHOXYBENZYLOXY)ACETIC ACID;Acetic acid, 2-[(4-methoxyphenyl)methoxy]-
CBNumber:
CB5479595
Molecular Formula:
C10H12O4
Molecular Weight:
196.2
MDL Number:
MFCD01861881
MOL File:
88920-24-5.mol
MSDS File:
SDS
Last updated:2026-05-28 02:52:02

(4-Methoxybenzyloxy)acetic acid Properties

Melting point 50.8-51.8 °C(Solv: ethyl ether (60-29-7); ligroine (8032-32-4))
Boiling point 367.4±22.0 °C(Predicted)
Density 1.198±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Solid
pka 3.40±0.10(Predicted)
color White to Off-White

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
HS Code  2918999090

(4-Methoxybenzyloxy)acetic acid price More Price(50)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC TRC-M331513-50MG 2-((4-Methoxybenzyl)oxy)acetic Acid 88920-24-5 50mg $65 2026-06-03 Buy
TRC TRC-M331513-500MG 2-((4-Methoxybenzyl)oxy)acetic Acid 88920-24-5 500mg $193 2026-06-03 Buy
TRC TRC-M331513-100MG 2-((4-Methoxybenzyl)oxy)acetic Acid 88920-24-5 100mg $78 2026-06-03 Buy
Apolloscientific OR939102 2-((4-Methoxybenzyl)oxy)acetic acid 98% 88920-24-5 1g $21 2026-06-04 Buy
Apolloscientific OR939102 2-((4-Methoxybenzyl)oxy)acetic acid 98% 88920-24-5 5g $71 2026-06-04 Buy
Product number Packaging Price Buy
TRC-M331513-50MG 50mg $65 Buy
TRC-M331513-500MG 500mg $193 Buy
TRC-M331513-100MG 100mg $78 Buy
OR939102 1g $21 Buy
OR939102 5g $71 Buy

(4-Methoxybenzyloxy)acetic acid Chemical Properties, Uses, Production

Synthesis

Bromoacetic acid

79-08-3

4-Methoxybenzyl alcohol

105-13-5

(4-Methoxybenzyloxy)acetic acid

88920-24-5

4-Methoxybenzyl alcohol (1 eq.) and bromoacetic acid (1.2 eq.) were dissolved in anhydrous tetrahydrofuran at 0 °C. Sodium hydride (60% w/w, mineral oil dispersion, 3 eq.) was added in three batches. The reaction mixture was stirred at 70 °C for 4 hours. After cooling to room temperature, water was added and the resulting mixture was washed with hexane. The aqueous phase was acidified to pH 2 with 1N hydrochloric acid and subsequently extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification by silica gel column chromatography with hexane solution of 50% ethyl acetate as eluent gave (4-methoxybenzyloxy)acetic acid (0.51 g, 71% yield) as a colorless solid.1H NMR (500 MHz, CDCl3) δ 7.29 (m, 2H), 6.90 (m, 2H), 4.59 (s, 2H), 4.10 (s, 2H), 3.81 ( s, 3H).

References

[1] Bioorganic and medicinal chemistry letters, 2001, vol. 11, # 21, p. 2837 - 2841
[2] Synlett, 2012, vol. 23, # 19, p. 2845 - 2849
[3] Tetrahedron Letters, 2002, vol. 43, # 41, p. 7427 - 7429
[4] Patent: WO2014/144100, 2014, A2. Location in patent: Paragraph 00274
[5] Patent: WO2006/109729, 2006, A1. Location in patent: Page/Page column 138-139

(4-Methoxybenzyloxy)acetic acid Preparation Products And Raw materials

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(4-Methoxybenzyloxy)acetic acid Spectrum

(4-METHOXYBENZYLOXY)ACETIC ACID Acetic acid, 2-[(4-methoxyphenyl)methoxy]- 2-((4-Methoxybenzyl)oxy)acetic acid p-methoxybenzyloxy acetic acid 88920-24-5