ChemicalBook--->CAS DataBase List--->6515-58-8

6515-58-8

6515-58-8 Structure

6515-58-8 Structure
IdentificationMore
[Name]

3-(BROMOMETHYL)BENZOIC ACID
[CAS]

6515-58-8
[Synonyms]

3-(BROMOMETHYL)BENZOIC ACID
ART-CHEM-BB B019567
CHEMPACIFIC 41258
RARECHEM AL BO 0050
3-Carboxybenzyl Bromide
m-Bromomethylbenzoic Acid
NSC 57780
α-Bromo-m-toluic Acid
a-Bromo-m-toluic Acid
[Molecular Formula]

C8H7BrO2
[MDL Number]

MFCD00045839
[Molecular Weight]

215.04
[MOL File]

6515-58-8.mol
Chemical PropertiesBack Directory
[Melting point ]

151-152 °C
[Boiling point ]

338.1±25.0 °C(Predicted)
[density ]

1.635±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

DMSO, Methanol
[form ]

Solid
[pka]

4.08±0.10(Predicted)
[color ]

Off-White
[InChI]

InChI=1S/C8H7BrO2/c9-5-6-2-1-3-7(4-6)8(10)11/h1-4H,5H2,(H,10,11)
[InChIKey]

FTPAHNNMUYOHOB-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC=CC(CBr)=C1
[CAS DataBase Reference]

6515-58-8(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-36
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2916399090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Carbon tetrachloride-->N-Bromosuccinimide-->Dibutyl ether-->m-Toluic acid-->tert-Butyl peroxybenzoate-->3-(Bromomethyl)benzoyl bromide-->Ethyl 3-(bromomethyl)benzoate-->Ethyl 3-methylbenzoate-->Methyl 3-methylbenzoate-->Bromoform
[Preparation Products]

3-(Chloromethyl)benzoyl chloride-->Succinimide
Hazard InformationBack Directory
[Chemical Properties]

Off-White Solid
[Uses]

3-(Bromomethyl)benzoic Acid is a compound useful in organic synthesis and other pharmacological processes.
[Synthesis]

tert-Butyl peroxybenzoate

614-45-9

m-Toluic acid

99-04-7

3-(BROMOMETHYL)BENZOIC ACID

6515-58-8

a) A mixture of m-toluic acid (15.0 g, 110 mmol), N-bromosuccinimide (19.60 g, 110 mmol) and tert-butyl peroxybenzoate (2.1 mL, 110 mmol) was mixed in carbon tetrachloride (50 mL) and heated to reflux the reaction overnight. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure. The resulting residue was washed with carbon tetrachloride and subsequently vacuum filtered. The filtrate was evaporated to dryness to afford the white solid product 3-bromomethylbenzoic acid (12.57 g, 53% yield). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 7.93 (m, 2H), 7.43 (m, 2H), 4.55 (s, 2H).

[References]

[1] Patent: US2002/49316, 2002, A1
Spectrum DetailBack Directory
[Spectrum Detail]

3-(BROMOMETHYL)BENZOIC ACID(6515-58-8)1HNMR
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