Methyl 2-nitro-3,4,5-trimethoxybenzoate

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Names

[ Name ]:
Methyl 2-nitro-3,4,5-trimethoxybenzoate

[Synonym ]:
Methyl 6-nitro-3,4,5-trimethoxybenzoate
MFCD00007097
EINECS 225-794-8
3,4,5-trimethoxy-2-nitrobenzoic acid methyl ester
Benzoic acid,3,4,5-trimethoxy-2-nitro-,methyl ester
3,4,5-Trimethoxy-2-nitro-benzoesaeure-methylester
methyl-2-nitro-3,4,5-trimethoxybenzoate
Trimethylaether-nitrogallussaeure-methylester

Chemical & Physical Properties

[ Density]:
1.284g/cm3

[ Boiling Point ]:
420ºC at 760mmHg

[ Melting Point ]:
67-69ºC

[ Molecular Formula ]:
C₁₁H₁₃NO₇

[ Molecular Weight ]:
271.22300

[ Flash Point ]:
188.9ºC

[ Exact Mass ]:
271.06900

[ PSA ]:
99.81000

[ LogP ]:
1.93040

[ Index of Refraction ]:
1.523

Safety Information

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2918990090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2918990090

[ Summary ]:
2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Synthesis and bioactivities of 6,7,8-trimethoxy-N-aryl-4-aminoquinazoline derivatives.

Bioorg. Med. Chem. 15(20) , 6608-17, (2007)

A series of 4-aminoquinazoline derivatives is prepared by the nucleophilic substitution reaction of 6,7,8-trimethoxy-4-chloroquinazoline and aryl amine. The structures of the compounds are confirmed b...

Methyl 2-amino-3,4,5-trimethoxybenzoate
Methyl 2-bromo-3,4,5-trimethoxybenzoate
methyl 2-nitro-3-(3,4,5-trimethoxyphenyl)prop-2-enoate
methyl 2-(2-aminobenzamido)-3,4,5-trimethoxybenzoate
methyl 2,6-dichloro-3,4,5-trimethoxybenzoate
2-methyl-2,3,4,5-tetrahydro-1,5-benzothiazepine
2-(Aminomethyl)-6-(difluoromethyl)-3-methoxypyridine-5-methanol
2-(Aminomethyl)-3-bromo-4-(difluoromethyl)-5-(trifluoromethyl)pyridine
2-(Aminomethyl)-3-chloro-6-(difluoromethyl)pyridine-4-acetonitrile
2-(Aminomethyl)-4-(difluoromethyl)-3-hydroxypyridine-5-acetonitrile
2-(Aminomethyl)-4-(difluoromethyl)-3-fluoro-5-methoxypyridine
2-(Aminomethyl)-4-(difluoromethyl)-6-iodopyridine-3-carboxaldehyde
2-(2-Amino-5-(difluoromethyl)-3-hydroxypyridin-4-yl)acetic acid
2-Chloro-5-(difluoromethyl)-3-(trifluoromethoxy)isonicotinic acid
2-(2-(Difluoromethoxy)-4,6-difluorophenyl)acetic acid
2-Chloro-3-(difluoromethyl)-6-iodo-5-methylpyridine

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