ChemicalBook--->CAS DataBase List--->88-14-2

88-14-2

88-14-2 Structure

88-14-2 Structure
IdentificationMore
[Name]

2-Furoic acid
[CAS]

88-14-2
[Synonyms]

2-FURANCARBONYL CHLORIDE
2-FURANCARBOXYLIC ACID CHLORIDE
2-FUROYL CHLORIDE
AKOS BBS-00003923
FURAN-2-CARBONYL CHLORIDE
FUROYL CHLORIDE
TIMTEC-BB SBB004224
2-Furancarbosylicacid
a-Furoicacid
alpha-Furancarboxylic acid
alpha-furancarboxylicacid
Furancarbonylicacid
Furancarboxylic acid-(2)
furancarboxylicacid
Furoica
Kyselina 2-furoova
Kyselina pyroslizova
kyselina2-furoova
kyselinapyroslizova
2-FUROIC ACID 99.5%
[EINECS(EC#)]

208-422-9
[Molecular Formula]

C5H4O3
[MDL Number]

MFCD00003228
[Molecular Weight]

112.08
[MOL File]

88-14-2.mol
Chemical PropertiesBack Directory
[Appearance]

white to light yellow crystal powde
[Melting point ]

−2 °C(lit.)
[Boiling point ]

173-174 °C(lit.)
[density ]

1.324 g/mL at 25 °C(lit.)
[vapor pressure ]

13.732Pa at 25℃
[refractive index ]

n20/D 1.531(lit.)
[Fp ]

185 °F
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

37g/l
[form ]

Fine Crystalline Powder
[pka]

3.16(at 25℃)
[color ]

Off-white to beige
[Odor]

odorless
[Odor Type]

odorless
[Water Solubility ]

36 g/L (20 ºC)
[Merck ]

14,4307
[BRN ]

110149
[InChIKey]

SMNDYUVBFMFKNZ-UHFFFAOYSA-N
[LogP]

0.628 at 25℃
[Uses]

Substitute for chloropicrin in disinfecting grain elevators.
[CAS DataBase Reference]

88-14-2(CAS DataBase Reference)
[NIST Chemistry Reference]

2-Furancarboxylic acid(88-14-2)
[EPA Substance Registry System]

88-14-2(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

C,Xi
[Risk Statements ]

R34:Causes burns.
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection .
[RIDADR ]

UN 3265 8/PG 2
[WGK Germany ]

3
[RTECS ]

LV1763000
[F ]

10-19-21
[TSCA ]

Yes
[HS Code ]

29321900
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sodium chlorate-->Cupric oxide-->hypochlorous acid
[Preparation Products]

Lactic acid-->Furan-->Ascorbic Acid-->L-Lysine hydrochloride-->Ethyl maltol-->Monosodium glutamate-->2-Amino-5-chlorobenzophenone-->Mucobromic acid-->L-(+)Sodium glutamate-->2-BROMO-5-NITROFURAN-->1-(2-Furoyl)piperazine-->METHYL 5-(CHLOROMETHYL)-2-FUROATE-->5-Bromofuroic acid-->6-Hydroxy-1-naphthoic acid-->Terazosin-->2-Furoyl chloride-->6-METHOXY-1-NAPHTHOIC ACID-->5-Chloro-2-(methylamino)benzophenone-->Ethyl 2-furoate-->D-ARABINONIC ACID-->3-Methylfuran-->Methyl 2-furoate-->(Z)-alpha-(methoxyimino)furan-2-acetic acid
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

2-Furancarboxylic acid(88-14-2).msds
Hazard InformationBack Directory
[Hazard]

Strong irritant to eyes and skin.
[Chemical Properties]

white to light yellow crystal powde
[Application]

2-Furoic acid (FA) is a preservative, acting as a bactericide and fungicide. Some of the applications of 2-furoic acid include:
Synthesis of a single-molecule magnet, Mn11Gd2 based high-nuclearity heterometallic complex.
Synthesis of orally active antidiabetic vanadyl complex, bis(α-furancarboxylato)oxovanadium(IV).
As a ligand in the synthesis of luminescent 4f-3d heterometallic one-dimensional coordination polymers.
Synthesis of biocompatible multifunctional dextran furoate nanospheres.
FA is often used as a starting material for the production of furoate esters.
FA and its derivatives are also used in the production of nylons principally applied in biomedical researches.
[Definition]

ChEBI: A furoic acid having the carboxylic acid group located at position 2.
[Preparation]

2-furoic acid can be synthesized by the oxidation of furfural. The reaction was carried out at 45°C with vigorous stirring. The reactant is filtered to recover the catalyst copper oxide, the filtrate is acidified with 50% sulfuric acid to pH 3-2.5, suction filtered, washed with water, and dried to obtain 2-furoic acid.
[Flammability and Explosibility]

Notclassified
[storage]

Store at -20°C
[Purification Methods]

Crystallise the acid from hot water (charcoal), dry it at 120o for 2hours, then recrystallise it from CHCl3, and again dry it at 120o for 2hours. For use as a standard in volumetric analysis, good quality commercial acid should be crystallised from CHCl3 and dried as above or sublimed at 130-140o/50-60mm or less. [Beilstein 18 I 438, 18 II 265, 18 III/IV 3914, 18/6 V 102.]
Spectrum DetailBack Directory
[Spectrum Detail]

2-Furoic acid(88-14-2)MS
2-Furoic acid(88-14-2)1HNMR
2-Furoic acid(88-14-2)13CNMR
2-Furoic acid(88-14-2)IR1
2-Furoic acid(88-14-2)IR2
2-Furoic acid(88-14-2)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Furoic acid, 98%(88-14-2)
[Alfa Aesar]

2-Furoic acid, 98%(88-14-2)
[Sigma Aldrich]

88-14-2(sigmaaldrich)
[TCI AMERICA]

2-Furancarboxylic Acid,>98.0%(GC)(T)(88-14-2)
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