1,3-Dimethyluracil

Modify Date: 2024-01-02 11:53:21

1,3-Dimethyluracil Structure
1,3-Dimethyluracil structure
Common Name 1,3-Dimethyluracil
CAS Number 874-14-6 Molecular Weight 140.140
Density 1.2±0.1 g/cm3 Boiling Point 208.4±23.0 °C at 760 mmHg
Molecular Formula C6H8N2O2 Melting Point 119-122 °C(lit.)
MSDS Chinese USA Flash Point 84.3±15.0 °C

 Use of 1,3-Dimethyluracil


1,3-Dimethyluracil is a pyrimidone derives from a uracil. 1,3-Dimethyluracil found occasionally in human urine. 1,3-Dimethyluracil shows inhibition activity against hCA I and hCA II (human carbonic anhydrase) with Ki of 316.2 μM and 166.4 μM, respectively[1][2].

 Names

Name 1,3-Dimethyluracil
Synonym More Synonyms

 1,3-Dimethyluracil Biological Activity

Description 1,3-Dimethyluracil is a pyrimidone derives from a uracil. 1,3-Dimethyluracil found occasionally in human urine. 1,3-Dimethyluracil shows inhibition activity against hCA I and hCA II (human carbonic anhydrase) with Ki of 316.2 μM and 166.4 μM, respectively[1][2].
Related Catalog
References

[1]. Stoessel D, et al. Promising Metabolite Profiles in the Plasma and CSF of Early Clinical Parkinson's Disease. Front Aging Neurosci. 2018 Mar 5;10:51.

[2]. Güney M, et al. Synthesis and carbonic anhydrase inhibitory properties of novel uracil derivatives. Bioorg Med Chem Lett. 2015 Aug 15;25(16):3261-3.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 208.4±23.0 °C at 760 mmHg
Melting Point 119-122 °C(lit.)
Molecular Formula C6H8N2O2
Molecular Weight 140.140
Flash Point 84.3±15.0 °C
Exact Mass 140.058578
PSA 44.00000
LogP 0.40
Vapour Pressure 0.2±0.4 mmHg at 25°C
Index of Refraction 1.519

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi:Irritant;
Risk Phrases R36
Safety Phrases S22-S24/25-S39-S26
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933599090

 Synthetic Route

 Customs

HS Code 2933599090
Summary 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles28

More Articles
Excited state structures and decay dynamics of 1,3-dimethyluracils in solutions: resonance Raman and quantum mechanical calculation study.

J. Phys. Chem. B 117(39) , 11660-9, (2013)

The resonance Raman spectroscopic study of the excited state structural dynamics of 1,3-dimethyluracil (DMU), 5-bromo-1,3-dimethyluracil (5BrDMU), uracil, and thymine in water and acetonitrile were re...

Ionization of dimethyluracil dimers leads to facile proton transfer in the absence of hydrogen bonds.

Nature Chemistry 4(4) , 323-9, (2012)

Proton transfer is ubiquitous in chemistry and biology, occurring, for example, in proteins, enzyme reactions and across proton channels and pumps. However, it has always been described in the context...

The SO4(.-)-induced chain reaction of 1,3-dimethyluracil with peroxodisulphate.

Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 51(3) , 441-53, (1987)

The sulphate radical SO4(.-) reacts with 1,3-dimethyluracil (1,3-DMU) (k = 5 X 10(9) dm3 mol-1 s-1) thereby forming with greater than or equal to 90 per cent yield the 1,3-DMU C(5)-OH adduct radical 4...

 Synonyms

N1,N3-Dimethyluracil
1,3-dimethylpyrimidine-2,4-dione
2,4(1H,3H)-Pyrimidinedione, 1,3-dimethyl-
1,3-Dimethyl-2,4(1H,3H)-pyrimidinedione
MFCD00038065
1,3-dimethyluracil
Uracil, 1,3-dimethyl-
1,3-dimethylpyrimidine-2,4(1H,3H)-dione
EINECS 212-856-4
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