ChemicalBook--->CAS DataBase List--->56256-14-5

56256-14-5

56256-14-5 Structure

56256-14-5 Structure
IdentificationBack Directory
[Name]

4-Bromo-3-methoxybenzoic acid
[CAS]

56256-14-5
[Synonyms]

56256-14-5
56256-14-5
4-BROMO-3-METHOXYBEN
2-Bromo-5-carboxyanisole
4-Bromo-3-methoxybenzoic acid
4-BROMO-3-METHOXYBENZOIC ACID 98
Benzoic acid, 4-bromo-3-methoxy-
4-Bromo-3-methoxybenzoic acid 98%
2-Bromo-5-carboxyanisole, 4-Bromo-m-anisic acid
4-Bromo-3-methoxybenzoic acid ISO 9001:2015 REACH
[Molecular Formula]

C8H7BrO3
[MDL Number]

MFCD08436017
[MOL File]

56256-14-5.mol
[Molecular Weight]

231.04
Chemical PropertiesBack Directory
[Melting point ]

221-224
[Boiling point ]

333.7±27.0 °C(Predicted)
[density ]

1.625±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

crystalline solid
[pka]

3.85±0.10(Predicted)
[color ]

Off-white
Questions And AnswerBack Directory
[Uses]

4-Bromo-3-methoxybenzoic acid is an important fine organic chemical product, widely used in pharmaceuticals, pesticides, fragrances, petrochemicals and other fields. With the development of science and technology, it is playing an increasingly important role in the synthesis of drugs, liquid crystals and other fields.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[Hazard Codes ]

Xi
[RIDADR ]

UN2811
[Hazard Note ]

Irritant/Keep Cold
[HS Code ]

2918999090
Hazard InformationBack Directory
[Chemical Properties]

off-white powder
[Synthesis]

METHYL 4-BROMO-3-METHOXYBENZOATE

17100-63-9

4-Bromo-3-methoxybenzoic acid

56256-14-5

General procedure for the synthesis of 4-bromo-3-methoxybenzoic acid from methyl 4-bromo-3-methoxybenzoate: To a stirred solution of methyl 4-bromo-3-methoxybenzoate (11.2 g) in THF (130 mL) was added methanol (45 mL), water (45 mL), and a 1 M aqueous lithium hydroxide (140 mL) in sequence. The reaction mixture was stirred at room temperature for 1 hour. Upon completion of the reaction, the solvent was removed by rotary evaporator under reduced pressure. Water was added to the residue, followed by the dropwise addition of 1 N hydrochloric acid while cooling in an ice bath until the pH of the mixture reached 4. The precipitated solid product was collected by diafiltration, washed with water and dried under reduced pressure to give 10.1 g of the title compound 4-bromo-3-methoxybenzoic acid, which was used in the subsequent reaction without further purification.1H-NMR (300 MHz. DMSO-d6): δ[ppm] = 3.87 (s, 3H), 7.42 (dd, 1H), 7.50 (d, 1H), 7.68 (d, 1H), 13.21 (br s, 1H).

[References]

[1] Beilstein Journal of Organic Chemistry, 2016, vol. 12, p. 2267 - 2273
[2] Patent: US2003/45557, 2003, A1
[3] Patent: WO2011/64328, 2011, A1. Location in patent: Page/Page column 79-80
[4] Patent: WO2012/143329, 2012, A1. Location in patent: Page/Page column 89
[5] Patent: WO2013/87579, 2013, A1. Location in patent: Page/Page column 96; 97
Spectrum DetailBack Directory
[Spectrum Detail]

4-Bromo-3-methoxybenzoic acid(56256-14-5)1HNMR
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56518-42-4 35450-36-3 22921-68-2 99-58-1