Name | 2,3-dimethoxybenzylamine |
Synonyms | RARECHEM AL BW 0151 2,3-Dimethoxybenzyla 2,3-dimethoxybenzylamine 2,3-DIMETHOXYBENZYLAMINE (2,3-Dimethoxyphenyl)methylamine (2,3-Dimethoxyphenyl)methanamine (2,3-dimethoxyphenyl)methanamine 1-(2,3-dimethoxyphenyl)methanamine |
CAS | 4393-09-3 |
EINECS | 224-515-7 |
InChI | InChI=1/C9H13NO2/c1-11-8-5-3-4-7(6-10)9(8)12-2/h3-5H,6,10H2,1-2H3 |
Molecular Formula | C9H13NO2 |
Molar Mass | 167.21 |
Density | 1.13 g/mL at 25 °C (lit.) |
Melting Point | 229-230 °C(Solv: N,N-dimethylformamide (68-12-2)) |
Boling Point | 137 °C/11 mmHg (lit.) |
Flash Point | >230°F |
Vapor Presure | 0.00709mmHg at 25°C |
Appearance | Liquid |
Color | Clear colorless to pale yellow |
pKa | 9.12±0.10(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
Refractive Index | n20/D 1.54(lit.) |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection |
UN IDs | 2735 |
WGK Germany | 3 |
HS Code | 29222900 |
Hazard Class | IRRITANT |
Packing Group | III |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
use | 2,3-dimethoxybenzylamine is a very important amine compound, which can be used as a raw material for various industrial resins and products, and is also an important intermediate in the synthesis of drugs and fragrances. |
preparation | 14.0g anhydrous zinc chloride, 11.0g potassium borohydride and 150ml tetrahydrofuran are added into a 500ml round bottom flask, protected by nitrogen, stirred at room temperature for 2.5 hours, 60ml toluene and 13.0 g2, 3-dimethoxybenzoate are added, part of the solvent is heated and evaporated, reacted at 100 ℃ for 3.5 hours, cooled, and poured into 150mL 10% hydrochloric acid, then add 10% potassium hydroxide solution dropwise to pH 11, filter, extract the filtrate with ether (20ml), combine the extract, dry with anhydrous sodium sulfate, evaporate the ether, distill under reduced pressure, collect 6.72g of fraction at 151~152.5 ℃/13mmHg, and the yield of 2, 3-dimethoxybenzylamine is 71.9%. |