Glurate

Names

[ Name ]:
Glurate

[Synonym ]:
EINECS 221-511-7
5-Ketocaproic acid
5-Oxohexanoic Acid
4-Acetylbutyric Acid
4-Acetylbutyricacid
5-Ketohexanoic acid
Hexanoic acid,5-oxo
5-oxocaproic acid
4-acetyl-butanoic acid
MFCD00004412
5-oxo-hexanoic acid

Biological Activity

[Description]:

Glurate (4-Acetylbutyric acid; 5-Oxohexanoic acid) can be used to construct antiviral agents (acyclic nucleoside esters) (extracted from patent WO1997030052A1)[1].

[Related Catalog]:

Research Areas >> Infection

Signaling Pathways >> Others >> Others

[References]

[1]. Per Engelhardt, et al. Synthesis of acyclic nucleosides. Patent WO1997030052A1.

Chemical & Physical Properties

[ Density]:
1.09 g/mL at 25 °C(lit.)

[ Boiling Point ]:
274-275 °C(lit.)

[ Melting Point ]:
13-14 °C(lit.)

[ Molecular Formula ]:
C₆H₁₀O₃

[ Molecular Weight ]:
130.14200

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
130.06300

[ PSA ]:
54.37000

[ LogP ]:
0.83030

[ Index of Refraction ]:
n20/D 1.4451(lit.)

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Risk Phrases ]:
R36/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2918300090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2918300090

[ Summary ]:
2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Identification of 5-hydroxyhexanoic acid, 4-hydroxyheptanoic acid and 4-hydroxyoctanoic acid as new constituents of bacterial polyhydroxyalkanoic acids. Valentin HE, et al.

Appl. Microbiol. Biotechnol. 46(3) , 261-267, (1996)

Proline-like β-turn mimics accessed via Ugi reaction involving monoprotected hydrazines. Krasavin M, et al.

Tetrahedron Lett. 51(10) , 1367-70, (2010)

A versatile and concise route to functionally substituted ?-butyrolactones and spiro-XXX-butyrolactones (lactone annelation) Mandal AK and Jawalkar DG

Tetrahedron Lett. 27.1 , 99-100, (1986)

Related Compounds

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