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| 3,5-Dichlorobenzoyl chloride Basic information |
Product Name: | 3,5-Dichlorobenzoyl chloride | Synonyms: | 3,5-dichloro-benzoylchlorid;3,5-DICHLOROBENZOYL CHLORIDE;DICHLOROBENZOYLCHLORIDE(3,5-);BENZOYL CHLORIDE, 3,5-DICHLORO-;BUTTPARK 45\07-36;DCBC;Benzoyl chloride, 3,5-dichloro- (7CI,8CI,9CI);3,5-Dichlorobenzoyl | CAS: | 2905-62-6 | MF: | C7H3Cl3O | MW: | 209.46 | EINECS: | 220-813-6 | Product Categories: | Acid Halides;Building Blocks;ACIDHALIDE;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Acid Halides;Carbonyl Compounds;Organic Building Blocks | Mol File: | 2905-62-6.mol | |
| 3,5-Dichlorobenzoyl chloride Chemical Properties |
Melting point | 28 °C (lit.) | Boiling point | 135-137 °C/25 mmHg (lit.) | density | 135 | vapor pressure | 0.1 mm Hg ( 32 °C) | refractive index | n20/D 1.582(lit.) | Fp | >230 °F | storage temp. | Refrigerator (+4°C) | solubility | soluble in Benzene,Toluene | form | powder to lump to clear liquid | color | White or Colorless to Almost white or Almost colorless | Sensitive | Moisture Sensitive | BRN | 1940681 | InChIKey | GGHLXLVPNZMBQR-UHFFFAOYSA-N | LogP | 3.32 | CAS DataBase Reference | 2905-62-6(CAS DataBase Reference) | NIST Chemistry Reference | 3,5-Dichlorobenzoyl chloride(2905-62-6) | EPA Substance Registry System | Benzoyl chloride, 3,5-dichloro- (2905-62-6) |
Hazard Codes | C | Risk Statements | 34-36/37 | Safety Statements | 26-27-28-36/37/39-45 | RIDADR | UN 3261 8/PG 2 | WGK Germany | 3 | RTECS | DM6636766 | Hazard Note | Corrosive | TSCA | T | HazardClass | 8 | PackingGroup | II | HS Code | 29163900 |
| 3,5-Dichlorobenzoyl chloride Usage And Synthesis |
Chemical Properties | clear colorless to light yellow liquid or low | Uses | 3,5-Dichlorobenzoyl chloride is a useful intermediate for organic synthesis and other pharmaceutical processes. | Uses | 3,5-Dichlorobenzoyl chloride has been used in the preparation of:
- N-(1,1-dimethylpropynyl)-3,5-dichlorobenzamide, herbicide
- (3,5-dichlorophenyl)(2-(4-methoxyphenyl)-5-methylbenzofuran-3-yl)methanone
| Flammability and Explosibility | Nonflammable | Synthesis | 3,5-Dichlorobenzoyl chloride is obtained by reacting by aryl carboxylic acid with DMF.Dissolve aryl carboxylic acid (10.0 mmol) in 50 mL DCM with drops of DMF
to a 100 mL roundbottomed flask. Cool the mixture to 0°C. Add oxalyl
chloride (20.0 mmol, 2.0 equivalents) dropwise to the reaction mixture.
Allow the reaction mixture to react for another 4 hours. Concentrate the
solvent in vacuo. Use the remaining residue directly. Fig The synthetic method of 3,5-Dichlorobenzoyl chloride |
| 3,5-Dichlorobenzoyl chloride Preparation Products And Raw materials |
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