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| | 3,4-Dichlorobenzylamine Basic information |
| Product Name: | 3,4-Dichlorobenzylamine | | Synonyms: | 3,4-DICHLOROBENZYLAMINE FOR SYNTHESIS;3,4-DICHLOROBENZYLAMINE;RARECHEM AL BW 0352;3,4-dichloro-benzenemethanamin;3,4-DICHLOROBENZYLAMINE 98%;(3,4-dichlorophenyl)methanamine;(3,4-dichlorophenyl)methylammonium;3,4-Dichlorobenzylam | | CAS: | 102-49-8 | | MF: | C7H7Cl2N | | MW: | 176.04 | | EINECS: | 203-035-1 | | Product Categories: | Building Blocks;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Amines;C7;Nitrogen Compounds;Isoxazoles ,Oxazoles;Anilines, Aromatic Amines and Nitro Compounds | | Mol File: | 102-49-8.mol |  |
| | 3,4-Dichlorobenzylamine Chemical Properties |
| Melting point | 332-333 °C(Solv: N,N-dimethylformamide (68-12-2)) | | Boiling point | 80-82 °C (0.6 mmHg) | | density | 1.32 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.578(lit.) | | Fp | >230 °F | | storage temp. | Keep in dark place,Inert atmosphere,2-8°C | | pka | 8.56±0.10(Predicted) | | form | Liquid | | Specific Gravity | 1.322 | | color | Clear colorless to light yellow | | Sensitive | Air Sensitive | | BRN | 508818 | | InChI | 1S/C7H7Cl2N/c8-6-2-1-5(4-10)3-7(6)9/h1-3H,4,10H2 | | InChIKey | IXHNFOOSLAWRBQ-UHFFFAOYSA-N | | SMILES | NCc1ccc(Cl)c(Cl)c1 | | CAS DataBase Reference | 102-49-8(CAS DataBase Reference) | | EPA Substance Registry System | Benzenemethanamine, 3,4-dichloro- (102-49-8) |
| Hazard Codes | C,Xi | | Risk Statements | 34 | | Safety Statements | 23-26-36/37/39-45 | | RIDADR | UN 2735 8/PG 3 | | WGK Germany | 3 | | Hazard Note | Irritant/Air Sensitive | | TSCA | TSCA listed | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29214990 | | Storage Class | 8A - Combustible corrosive hazardous materials | | Hazard Classifications | Eye Dam. 1
Skin Corr. 1B |
| | 3,4-Dichlorobenzylamine Usage And Synthesis |
| Chemical Properties | clear colorless to light yellow liquid | | Uses | 3,4-Dichlorobenzylamine is a benzylamine compound. Benzylamines are a class of small-molecule compounds with simple structures, widely present in the biological world, with extremely important physiological and pharmacological activities, and are widely used in the research and development of antibacterial drugs. For example, the antifungal drugs terbinafine and butenafine all have the structure of benzylamine. | | Synthesis | Using 3,4-dichlorobenzyl azide (5 mmol, 1.01 g) as raw material, dichloromethane (25 mL) was added to a 100 mL reaction flask and a dichloromethane (25 mL) solution of boron tribromide (20 mmol, 5.00 g) was slowly added dropwise under nitrogen protection. After the dropwise addition, the reaction was stirred at 25 °C for 6 hours. Upon completion of the reaction, the reaction was quenched by the addition of methanol (25 mL) and stirring was continued for 0.5 hours. After the reaction solution was clarified, the reaction solution was concentrated by rotary evaporator. The resulting crude product was recrystallized using a mixed solvent of methanol/ether to give the title compound 3,4-dichlorobenzylamine in white solid form in 89% yield (0.778 g). | | References | [1] Patent: CN108409580, 2018, A. Location in patent: Paragraph 0044; 0045; 0046 |
| | 3,4-Dichlorobenzylamine Preparation Products And Raw materials |
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