4-Bromobenzoyl chloride | Pharmaceutical Grade | 99.99% Purity | 10mg 20mg 30mg Vials | CAS 586-75-4

4-Bromobenzoyl chloride Basic information
Product Name: 4-Bromobenzoyl chloride
Synonyms: 4-BroMobenzoyl Chloride, 97+%;The broMine benzoyl chloride;P-BROMOBENZOYL CHLORIDE;4-BROMOBENZOYL CHLORIDE;AKOS BBS-00003926;4-Brorobenzoylchloride;4-Bromobenzoyl chlor;Of broMine chloride
CAS: 586-75-4
MF: C7H4BrClO
MW: 219.46
EINECS: 209-580-1
Product Categories: Pyridines ,Halogenated Heterocycles;Acid Halides;Absolute Configuration Determination (Exciton Chirality CD Method);Analytical Chemistry;Carbonyl Compounds;Organic Building Blocks;Aromatic Halides (substituted);Enantiomer Excess & Absolute Configuration Determination;Exciton Chirality CD Method (for Hydroxyl Groups);K00001
Mol File: 586-75-4.mol
Shop 4-Bromobenzoyl chloride586-75-4-Detailed Image 1

4-Bromobenzoyl chloride Chemical Properties
Melting point 36-39 °C(lit.)
Boiling point 246 °C
density 1.6111 (rough estimate)
refractive index 1.5963 (estimate)
Fp >230 °F
storage temp. 2-8°C
solubility Chloroform, Methanol (Slightly)
form Low Melting Solid
color White to light brown
Water Solubility Soluble in methanol. Reacts with water forming Hcl.
Sensitive Moisture Sensitive
BRN 636641
Stability: Moisture Sensitive
InChI 1S/C7H4BrClO/c8-6-3-1-5(2-4-6)7(9)10/h1-4H
InChIKey DENKGPBHLYFNGK-UHFFFAOYSA-N
SMILES ClC(=O)c1ccc(Br)cc1
CAS DataBase Reference 586-75-4(CAS DataBase Reference)
NIST Chemistry Reference Benzoyl chloride, 4-bromo-(586-75-4)
EPA Substance Registry System Benzoyl chloride, 4-bromo- (586-75-4)

Safety Information
Hazard Codes C
Risk Statements 34-37
Safety Statements 26-36/37/39-45
RIDADR UN 3261 8/PG 2
WGK Germany 3
F 19-21
TSCA TSCA listed
HazardClass 8
PackingGroup II
HS Code 29163900
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Eye Dam. 1
Skin Corr. 1B
MSDS Information
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4-Bromobenzoyl chloride Usage And Synthesis
Chemical Properties White to light brown low melting solid
Uses 4-Bromobenzoyl chloride is used in the synthesis of HIV-1 protease inhibitors. It is also used in the synthesis of oxazoles, cyclohexanone derivatives as analgesic and antimicrobial agents.
Purification Methods Check IR of a film to see if OH bands are present. If absent then recrystallise from pet ether and dry it in vacuo. If OH bands are weak, then distil it in vacuo and recrystallise if necessary. If OH bands are very strong, then treat with an equal volume of redistilled SOCl2 reflux for 2hours, then evaporate excess of SOCl2 and distil the residual oil or low melting solid. Store it in the dark away from moisture. LACHRYMATORY. [Martin & Partington J Chem Soc 1175 1936, Beilstein 9 IV 1023.]

4-Bromobenzoyl chloride Preparation Products And Raw materials
Preparation Products 2-(4-BROMOPHENYL)-5-(1-NAPHTHYL)-1,3,4-OXADIAZOLE-->2-(4-BROMOPHENYL)-5-PHENYL-1,3,4-OXADIAZOLE-->4-BROMO-4'-METHOXYBENZOPHENONE-->2-(4-BROMO-PHENYL)-1H-IMIDAZOLE-->1-(4-bromophenyl)-2-chloroethan-1-one-->3-(4-BROMO-PHENYL)-3-OXO-PROPIONIC ACID METHYL ESTER-->4-BROMO-3'-CHLOROBENZOPHENONE-->Methanone, (4-bromophenyl)-1H-indol-3-yl--->4-bromo-N-(6-methylpyridin-2-yl)benzamide-->4-BroMo-N,N-dicyclohexylbenzaMide, 97%-->N-(2-aminoethyl)-4-bromobenzamide-->4-bromo-N-(3,4-dimethoxyphenyl)benzamide