2,4-Dimethoxybenzylamine
Names
[ CAS No. ]:
20781-20-8
[ Name ]:
2,4-Dimethoxybenzylamine
[Synonym ]:
2,4-BIPYRIDINE-6-CARBOXYLIC ACID
Benzenemethanamine, 2,5-dimethoxy-
(2,4-Dimethoxyphenyl)methanamine
2,4-dimethoxy-benzylamine
Benzenemethanamine, 2,4-dimethoxy-
1-(2,5-Dimethoxyphenyl)methanamine
1-(2,4-Dimethoxyphenyl)methanamine
MFCD00052811
2,4-dimethoxybenzylamine
2,4-DIMETHOXYBENZYL AMINE
Chemical & Physical Properties
[ Density]:
1.1±0.1 g/cm3
[ Boiling Point ]:
272.4±25.0 °C at 760 mmHg
[ Molecular Formula ]:
C9H13NO2
[ Molecular Weight ]:
167.205
[ Flash Point ]:
128.4±30.4 °C
[ Exact Mass ]:
167.094635
[ PSA ]:
44.48000
[ LogP ]:
0.97
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.523
MSDS
Safety Information
[ Symbol ]:
GHS05
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H314
[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
C:Corrosive;
[ Risk Phrases ]:
R34
[ Safety Phrases ]:
S26-S27-S36/37/39-S45
[ RIDADR ]:
UN 2735 8/PG 3
[ WGK Germany ]:
3
[ RTECS ]:
DP4430000
[ Packaging Group ]:
III
[ Hazard Class ]:
8
[ HS Code ]:
2922299090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2922299090
[ Summary ]:
2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
J. Org. Chem. 75(5) , 1366-77, (2010)
Full details of the first total synthesis of (-)-muraymycin (MRY) D2 and its epimer, the antibacterial nucleoside natural product, are described. Key strategic elements of the approach include the pre...
Application of the Ugi reaction for the one-pot synthesis of uracil polyoxin C analogues.J. Org. Chem. 74(13) , 4870-3, (2009)
A simple, two-step synthesis of amide derivatives of uracil polyoxin C (UPOC) methyl ester using the Ugi reaction is described. The four components employed in the Ugi reaction are 2',3'-isopropylidin...
Synthesis of N-hydroxythiourea.J. Med. Chem. 19(2) , 336-7, (1976)
The synthesis of the title compound (1) was accomplished by the conversion of 2,4-dimethoxybenzylamine (2) into an isothiocyanate (3) using thiocarbonyl diimidazole. Treatment of 3 with hydroxylamine ...