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Methyl 5-methoxy-2-nitrobenzoate

CAS No.
2327-45-9
Chemical Name:
Methyl 5-methoxy-2-nitrobenzoate
Synonyms
5-Methoxy-2-nitroMethylbenzoate;METHYL 5-METHOXY-2-NITROBENZOATE;Methyl5-methoxy-2-nitrobenzoate98%;Methyl 5-methoxy-2-nitrobenzoate 98%;5-Methoxy-2-nitro-benzoic acid methyl ester;Benzoic acid,5-Methoxy-2-nitro-, Methyl ester
CBNumber:
CB2142605
Molecular Formula:
C9H9NO5
Molecular Weight:
211.17
MDL Number:
MFCD00662902
MOL File:
2327-45-9.mol
MSDS File:
SDS
Last updated:2026-05-27 23:55:49

Methyl 5-methoxy-2-nitrobenzoate Properties

Melting point 58-59 °C
Boiling point 196-198 °C(Press: 15-16 Torr)
Density 1.294±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form crystals
color Light lemon/yellow, granular

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
Hazard Codes  Xi
Hazard Note  Irritant
HS Code  2918300090

Methyl 5-methoxy-2-nitrobenzoate price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Apolloscientific OR7411 Methyl 5-methoxy-2-nitrobenzoate 98% 2327-45-9 5g $21 2026-06-04 Buy
Apolloscientific OR7411 Methyl 5-methoxy-2-nitrobenzoate 98% 2327-45-9 25g $35 2026-06-04 Buy
Apolloscientific OR7411 Methyl 5-methoxy-2-nitrobenzoate 98% 2327-45-9 100g $131 2026-06-04 Buy
aablocks AA002MNP Methyl 5-methoxy-2-nitrobenzoate 98% 2327-45-9 5g $11 2026-05-28 Buy
aablocks AA002MNP Methyl 5-methoxy-2-nitrobenzoate 98% 2327-45-9 10g $15 2026-05-28 Buy
Product number Packaging Price Buy
OR7411 5g $21 Buy
OR7411 25g $35 Buy
OR7411 100g $131 Buy
AA002MNP 5g $11 Buy
AA002MNP 10g $15 Buy

Methyl 5-methoxy-2-nitrobenzoate Chemical Properties,Uses,Production

Description

Methyl 5-methoxy-2-nitrobenzoate is an important organic intermediate, commonly used in organic synthesis. This compound can be synthesized from 5-Hydroxy-2-nitrobenzoic acid.

Synthesis

Methanol

67-56-1

5-Methoxy-2-nitrobenzoic acid

1882-69-5

Methyl 5-methoxy-2-nitrobenzoate

2327-45-9

To a pressure-resistant reaction flask was added 5-methoxy-2-nitrobenzoic acid (3.98 g, 20.0 mmol) and anhydrous methanol (10 mL). Concentrated sulfuric acid (150 μL) was added slowly and dropwise. The reaction vial was sealed and the reaction was stirred at 85 °C for 4 days. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure to half the original volume. Ethyl acetate (25 mL) was added to dilute, and the organic phase was washed sequentially with water (25 mL), saturated aqueous sodium bicarbonate solution (2 × 25 mL), saturated saline (2 × 25 mL) and water (2 × 25 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford methyl 5-methoxy-2-nitrobenzoate as a yellow oil (3.57 g, 87% yield). Its nuclear magnetic resonance hydrogen spectrum (1H NMR, 300 MHz, CDCl3) data were as follows: δ 8.04 (d, J = 8.8 Hz, 1H, H-6), 7.04 (d, J = 2.3 Hz, 1H, H-3), 7.00 (dd, J = 8.8, 2.8 Hz, 1H, H-4), 3.93 (s, 3H, OCH3), 3.91 (s. 3H, OCH3). The nuclear magnetic resonance carbon spectrum (13C NMR, 75 MHz, CDCl3) data were as follows: δ 166.7, 163.5, 140.2, 131.4, 126.8, 115.9, 114.2, 56.4, 53.5. The obtained data are in agreement with the literature reports.

References

[1] Synlett, 2016, vol. 27, # 8, p. 1237 - 1240
[2] Patent: WO2005/121152, 2005, A1. Location in patent: Page/Page column 30

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View Lastest Price from Methyl 5-methoxy-2-nitrobenzoate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
METHYL 5-METHOXY-2-NITROBENZOATE pictures 2019-07-12 METHYL 5-METHOXY-2-NITROBENZOATE
2327-45-9
$1.00 1KG 99% 100kg Career Henan Chemical Co

Methyl 5-methoxy-2-nitrobenzoate Spectrum

Benzoic acid,5-Methoxy-2-nitro-, Methyl ester 5-Methoxy-2-nitroMethylbenzoate 5-Methoxy-2-nitro-benzoic acid methyl ester Methyl5-methoxy-2-nitrobenzoate98% METHYL 5-METHOXY-2-NITROBENZOATE Methyl 5-methoxy-2-nitrobenzoate 98% 2327-45-9 Acids & Esters Anisoles, Alkyloxy Compounds & Phenylacetates Nitro Compounds blocks Carboxes NitroCompounds Aromatic Esters