Basic information Safety Supplier Related

2,3-Dimethoxybenzylamine

Basic information Safety Supplier Related

2,3-Dimethoxybenzylamine Basic information

Product Name:
2,3-Dimethoxybenzylamine
Synonyms:
  • (2,3-Dimethoxyphenyl)methanamine
  • RARECHEM AL BW 0151
  • 2,3-DIMETHOXYBENZYLAMINE
  • 2,3-Dimethoxybenzylamine ,99%
  • 2,3-Dimethoxybenzyla
  • (2,3-Dimethoxyphenyl)methylamine
  • 4393/9/3
  • 2,3-Dimethoxybenzylamine 99%
CAS:
4393-09-3
MF:
C9H13NO2
MW:
167.21
EINECS:
224-515-7
Product Categories:
  • Amines
  • C9 to C10
  • Anilines, Aromatic Amines and Nitro Compounds
  • Amine
  • Nitrogen Compounds
Mol File:
4393-09-3.mol
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2,3-Dimethoxybenzylamine Chemical Properties

Melting point:
229-230 °C(Solv: N,N-dimethylformamide (68-12-2))
Boiling point:
137 °C/11 mmHg (lit.)
Density 
1.13 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.54(lit.)
Flash point:
>230 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
9.12±0.10(Predicted)
form 
Liquid
color 
Clear colorless to pale yellow
CAS DataBase Reference
4393-09-3(CAS DataBase Reference)
NIST Chemistry Reference
Benzenemethanamine, 2,3-dimethoxy-(4393-09-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
RIDADR 
2735
WGK Germany 
3
HazardClass 
IRRITANT
PackingGroup 
III
HS Code 
29222900

MSDS

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2,3-Dimethoxybenzylamine Usage And Synthesis

Chemical Properties

Colorless to light yellowliqui

Uses

2,3-Dimethoxybenzylamine was used in the synthesis of di-,tri- and tetrapeptide linked dicatechol derivatives and 1-aryl-2,3-dihydro-1H-isoindoles (isoindolines).

Synthesis

Add 14.0g of anhydrous zinc chloride, 11.0g of potassium borohydride and 150ml of tetrahydrofuran into a 500ml round bottom flask, protected by nitrogen, stirred at room temperature for 2.5 hours, add 60ml of toluene and 13.0g of 2,3-dimethoxybenzoic acid amine, evaporate part of the solvent with heat and react at 100 for 3.5 hours, after cooling, pour into 150mL of 10% hydrochloric acid, then dropwise add 10% potassium hydroxide solution to pH 11, filtered, the filtrate was extracted with ether (20 ml), the extracts were combined, dried with anhydrous sodium sulfate, evaporated off the ether, distilled under reduced pressure, and 6.72 g of the fractions at 151~152.5 C/13 mmHg were collected, 71.9% yield of 2,3-dimethoxybenzylamine.

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