2,4-Dimethoxybenzylamine 20781-20-8 CAS NO.20781-20-8

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2,4-Dimethoxybenzylamine Basic information

Product Name:	2,4-Dimethoxybenzylamine
Synonyms:	RARECHEM AL BW 0348;RARECHEM AL BW 0153;AURORA KA-7637;2,4-DIMETHOXYBENZYLAMINE;(2,4-dimethoxyphenyl)methanamine;[(2,4-Dimethoxyphenyl)methyl]amine;2,4-Dimethoxybenzenemethanamine;2,4-Dimethyloxybenzylamine
CAS:	20781-20-8
MF:	C9H13NO2
MW:	167.21
EINECS:	672-586-1
Product Categories:	Chemical Amines;Aromatics;Amine;Amines;C9 to C10;Nitrogen Compounds
Mol File:	20781-20-8.mol

2,4-Dimethoxybenzylamine Chemical Properties

Boiling point	95 °C0.2 mm Hg(lit.)
density	1.113 g/mL at 25 °C(lit.)
refractive index	n20/D 1.549(lit.)
Fp	>230 °F
storage temp.	under inert gas (nitrogen or Argon) at 2–8 °C
form	Liquid
pka	9.39±0.10(Predicted)
color	Clear colorless to slightly yellow
Sensitive	Air Sensitive
InChIKey	QOWBXWFYRXSBAS-UHFFFAOYSA-N
CAS DataBase Reference	20781-20-8(CAS DataBase Reference)

Safety Information

Hazard Codes	C
Risk Statements	34
Safety Statements	26-27-36/37/39-45
RIDADR	UN 2735 8/PG 3
WGK Germany	3
RTECS	DP4430000
HazardClass	8
PackingGroup	III
HS Code	29222990

MSDS Information

Provider	Language
SigmaAldrich	English
ACROS	English

2,4-Dimethoxybenzylamine Usage And Synthesis

Chemical Properties	Colorless to light yellow liqui
Uses	2,4-Dimethoxybenzylamine is an amine nucleophile used to investigate the 1,4- reactivity of 5-bromo-2-indene-1-one. It may be used in the following studies: As an ammonia equivalent in the concise synthesis of a series of 2,4,5-trisubstituted oxazoles, via a tandem Ugi/Robinson-Gabriel reaction sequence. Total synthesis of (-)-muraymycin (MRY) D2 and its epimer, the antibacterial nucleoside natural product. Two-step synthesis of amide derivatives of uracil polyoxin C (UPOC) methyl ester using the Ugi reaction. Synthesis of N-hydroxythiourea. Synthesis of anti-HIV-1 agents.
General Description	2,4-Dimethoxybenzylamine can be preprepared by reduction (NaBH4 , BF3.OEt2, THF) of 2,4-dimethoxybenzonitrile.

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