Glurate

Modify Date: 2024-01-02 18:23:48

Glurate Structure
Glurate structure
Common Name Glurate
CAS Number 3128-06-1 Molecular Weight 130.14200
Density 1.09 g/mL at 25 °C(lit.) Boiling Point 274-275 °C(lit.)
Molecular Formula C6H10O3 Melting Point 13-14 °C(lit.)
MSDS Chinese USA Flash Point >230 °F

 Use of Glurate


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

 Names

Name 5-oxohexanoic acid
Synonym More Synonyms

 Glurate 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
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.)

 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

 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%

 Articles5

More 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)

 Synonyms

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