BENZOIC ACID, 4-BROMO-2-(HYDROXYMETHYL)-
- Product Name
- BENZOIC ACID, 4-BROMO-2-(HYDROXYMETHYL)-
- CAS No.
- 670256-21-0
- Chemical Name
- BENZOIC ACID, 4-BROMO-2-(HYDROXYMETHYL)-
- Synonyms
- 4-Bromo-alpha-hydroxy-o-toluic acid;4-BroMo-2-(hydroxyMethyl)benzoic acid;BENZOIC ACID, 4-BROMO-2-(HYDROXYMETHYL)-
- CBNumber
- CB52467705
- Molecular Formula
- C8H7BrO3
- Formula Weight
- 231.04
- MOL File
- 670256-21-0.mol
BENZOIC ACID, 4-BROMO-2-(HYDROXYMETHYL)- Property
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- White to off-white Solid
Safety
- HS Code
- 2918199890
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- OR957980
- Product name
- 4-Bromo-2-(hydroxymethyl)benzoicacid
- Purity
- 95+%
- Packaging
- 100mg
- Price
- $102
- Updated
- 2021/12/16
- Product number
- OR957980
- Product name
- 4-Bromo-2-(hydroxymethyl)benzoicacid
- Purity
- 95+%
- Packaging
- 250mg
- Price
- $161
- Updated
- 2021/12/16
- Product number
- 9284DA
- Product name
- 4-Bromo-2-(hydroxymethyl)benzoicacid
- Packaging
- 250mg
- Price
- $240
- Updated
- 2021/12/16
- Product number
- CM123559
- Product name
- 4-bromo-2-(hydroxymethyl)benzoicacid
- Purity
- 95%
- Packaging
- 1g
- Price
- $337
- Updated
- 2021/12/16
- Product number
- CD12044537
- Product name
- 4-Bromo-2-(hydroxymethyl)benzoicacid
- Purity
- 95+%
- Packaging
- 1g
- Price
- $356
- Updated
- 2021/12/16
BENZOIC ACID, 4-BROMO-2-(HYDROXYMETHYL)- Chemical Properties,Usage,Production
Synthesis
64169-34-2
670256-21-0
The general procedure for the synthesis of 4-bromo-2-hydroxymethylbenzoic acid using 5-bromophthalide as starting material was as follows: 5-bromophthaloyl (9 g, 0.042 mol) was dissolved in methanol (150 ml), 2N aqueous sodium hydroxide (100 ml) was added, and the reaction was carried out at reflux overnight. After completion of the reaction, the reaction mixture was concentrated under reduced pressure. The concentrate was diluted with water and acidified with dilute hydrochloric acid to appropriate pH. The precipitated solid precipitate was collected by filtration and the residue was washed sequentially with cold water and cold ethyl acetate and dried to give 4-bromo-2-hydroxymethylbenzoic acid (9.7 g, 100% yield) as a white solid.
References
[1] Patent: US2008/15237, 2008, A1. Location in patent: Page/Page column 33
[2] Journal of Medicinal Chemistry, 2018, vol. 61, # 16, p. 7144 - 7167
[3] Patent: WO2015/89327, 2015, A1. Location in patent: Paragraph 0375
[4] Bulletin de la Societe Chimique de France, 1954, p. 769,772
[5] Journal of the Chemical Society, 1931, p. 867,869
BENZOIC ACID, 4-BROMO-2-(HYDROXYMETHYL)- Preparation Products And Raw materials
Raw materials
Preparation Products
BENZOIC ACID, 4-BROMO-2-(HYDROXYMETHYL)- Suppliers
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