ChemicalBook--->CAS DataBase List--->33890-03-8

33890-03-8

33890-03-8 Structure

33890-03-8 Structure
IdentificationBack Directory
[Name]

4-Aminoisophthalic acid
[CAS]

33890-03-8
[Synonyms]

-Aminoisophthalic acid
4-Aminoisophthalic acid
5-Carboxyanthranilic acid
4-aminobenzene-1,3-dicarboxylicaci
4-Amino-1,3-benzenedicarboxylic acid
4-Aminobenzene-1,3-dicarboxylic acid
1,3-Benzenedicarboxylic acid, 4-amino-
[Molecular Formula]

C8H7NO4
[MDL Number]

MFCD00102008
[MOL File]

33890-03-8.mol
[Molecular Weight]

181.15
Chemical PropertiesBack Directory
[Melting point ]

336-337℃
[Boiling point ]

458.1±40.0 °C(Predicted)
[density ]

1.551
[storage temp. ]

RT, protect from light
[pka]

4.49±0.10(Predicted)
[Appearance]

Off-white to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

29173990
Hazard InformationBack Directory
[Chemical Properties]

Off-white powder
[Synthesis]

4-NITROISOPHTHALIC ACID

4315-09-7

4-Aminoisophthalic acid

33890-03-8

General procedure: 4-nitroisophthalic acid (98 g, 0.457 mol) was dissolved in methanol (5 L) and 20% Pd/C catalyst was added. The hydrogenation reaction was carried out at room temperature for 4 hours. Upon completion of the reaction, the mixture was filtered through diatomaceous earth to remove the catalyst. The filtrate was concentrated in vacuum to afford 4-aminoisophthalic acid (72 g, 87% yield) as a white solid. The product was detected by thin layer chromatography (TLC) with chloroform/methanol (7:3) as the unfolding agent and an Rf value of 0.4.

[References]

[1] Patent: WO2005/11686, 2005, A1. Location in patent: Page 38
[2] Patent: WO2004/7491, 2004, A1. Location in patent: Page 57
[3] Farmaco, Edizione Scientifica, 1984, vol. 39, # 11, p. 968 - 978
[4] Patent: US2008/280900, 2008, A1
[5] Patent: US6635657, 2003, B1
Spectrum DetailBack Directory
[Spectrum Detail]

4-Aminoisophthalic acid(33890-03-8)1HNMR
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