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89364-31-8

89364-31-8 Structure

89364-31-8 Structure
IdentificationBack Directory
[Name]

TETRAHYDRO-3-FUROIC ACID
[CAS]

89364-31-8
[Synonyms]

3-Tetrahydrofuroic
RARECHEM AL BE 0888
TETRAHYDRO-3-FUROIC ACID
oxolane-3-carboxylic acid
(?-Tetrahydro-3-furoic acid
3-Carboxylic tetrahydrofuran
Tetrahydrofuran-3-carboxy...
Tetrahydro-3-furoic acid ,99%
tetrahydro-3-furancarboxylic acid
TETRAHYDRO-3-FUROIC ACID, GC 97+%
TETRAHYDRO-FURAN-3-CARBOXYLIC ACID
3-Furancarboxylic acid, tetrahydro-
3-Furancarboxylicacid,tetrahydro-(9CI)
Oxolane-3-carboxylic acid, 3-Carboxytetrahydrofuran
Tetrahydro-3-furoic acid contains 250 ppM BHT as inhibitor, 99%
[Molecular Formula]

C5H8O3
[MDL Number]

MFCD00075173
[MOL File]

89364-31-8.mol
[Molecular Weight]

116.12
Chemical PropertiesBack Directory
[Melting point ]

129-130 °C
[Boiling point ]

140 °C15 mm Hg(lit.)
[density ]

1.214 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.4605(lit.)
[Fp ]

>230 °F
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

Acetone, Chloroform (Slightly)
[form ]

Liquid
[pka]

4.33±0.20(Predicted)
[color ]

Colorless to pale yellow
[InChI]

InChI=1S/C5H8O3/c6-5(7)4-1-2-8-3-4/h4H,1-3H2,(H,6,7)
[InChIKey]

BOTREHHXSQGWTR-UHFFFAOYSA-N
[SMILES]

O1CCC(C(O)=O)C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37/39
[WGK Germany ]

3
[HS Code ]

2932190090
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Raw materials And Preparation ProductsBack Directory
[Raw materials]

3-Furancarboxylic acid, tetrahydro-, phenylmethyl ester, (S)- (9CI)-->benzyl tetrahydrofuran-3-carboxylate-->Tetrahydrofuran-3-carboxaldehyde-->alpha-Methyl-gamma-butyrolactone
[Preparation Products]

Tetrahydro-furan-3-carbonyl chloride
Hazard InformationBack Directory
[Uses]

Tetrahydro-3-furoic Acid can be used in the synthesis of anti-tumor compounds comprising of hydroxyisovalerylshikonin analogs. Furthermore, the compound is a reagent in the synthesis of class II c-Met inhibitors, in the treatment of c-Met dependant tumors.
Spectrum DetailBack Directory
[Spectrum Detail]

TETRAHYDRO-3-FUROIC ACID(89364-31-8)1HNMR
TETRAHYDRO-3-FUROIC ACID(89364-31-8)FT-IR
TETRAHYDRO-3-FUROIC ACID(89364-31-8)IR
TETRAHYDRO-3-FUROIC ACID(89364-31-8)Raman
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