1-cyclohexyluracil

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Names

[ CAS No. ]:
712-43-6

[ Name ]:
1-cyclohexyluracil

[Synonym ]:
1-Cyclohexyluracyl
MFCD00038460
1-cyclohexyluracil
1-cyclohexyl-1H-pyrimidine-2,4-dione
N-Cyclohexyluracil

Chemical & Physical Properties

[ Density]:
1.214g/cm3

[ Molecular Formula ]:
C10H14N2O2

[ Molecular Weight ]:
194.23000

[ Exact Mass ]:
194.10600

[ PSA ]:
54.86000

[ LogP ]:
1.04180

[ Appearance of Characters ]:
faint yellow

[ Index of Refraction ]:
1.549

[ Storage condition ]:
2-8°C

Safety Information

[ Risk Phrases ]:
20/21/22

[ Safety Phrases ]:
3/7-36/37

[ HS Code ]:
2933599090

Precursor & DownStream

Precursor

DownStream

  • 3-cyclohexyl-5,5-difluoro-2,6-dioxohexahydropyrimidin-4-yl acetate
  • 3-cyclohexyl-5-fluoro-2,6-dioxohexahydropyrimidin-4-yl acetate
  • 1-cyclohexyl-5-fluoropyrimidine-2,4-dione

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%

Articles

Solvent-dependent photophysics of 1-cyclohexyluracil: ultrafast branching in the initial bright state leads nonradiatively to the electronic ground state and a long-lived 1npi* state.

J. Phys. Chem. B 110(37) , 18641-50, (2006)

The modified nucleic acid base, 1-cyclohexyluracil, was studied by femtosecond transient absorption spectroscopy in protic and aprotic solvents of varying polarity. UV excitation at 267 nm populates t...

Dynamic properties of interaction between nucleic acid bases and models of amino acids.

Biochem. Int. 18(1) , 189-95, (1989)

We have discussed the possible hydrogen bonding mode of adenine-uracil base dimers and peptide side chains, together with their characteristic effects on the stability of adenine-uracil base pairing i...

Fourier transform infrared spectroscopy of 1-cyclohexyluracil aggregates in CDCl(3) solutions.

J. Chem. Phys. 130(12) , 125102, (2009)

We reinvestigated the self-aggregation of 1-cyclohexyluracil (1CHU) in CDCl(3) solutions. Wavelength dependent absolute extinction coefficients of the monomer and of dimers are presented on the basis ...


More Articles

Related Compounds

  • 1-cyclohexyluracil
  • 1-cyclohexyl-2,6-dioxo-3H-pyrimidine-5-carbonitrile
  • 1-[2-(2-fluorobenzoyl)pyrrol-1-yl]propan-2-yl-dimethylazanium,chloride
  • 1-[2-(2-methoxybenzoyl)pyrrol-1-yl]propan-2-yl-dimethylazanium,chloride
  • 1-methyl-3-[3-[[methyl-[(4-nitrophenyl)methyl]carbamoyl]amino]phenyl]-1-[(4-nitrophenyl)methyl]urea
  • 1-(2-methoxyphenyl)-4-(2-phenylethyl)piperazine
  • Methyl (1S,3S,4R)-3-hydroxy-7-azabicyclo[2.2.1]heptane-1-carboxylate hydrochloride
  • (R)-4-(Difluoromethyl)-2-methoxy-5-(pyrrolidin-2-yl)phenol
  • Rel-tert-butyl (3aR,5r,6aS)-5-hydroxy-5-methylhexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
  • (2S)-2-(Fluoro(phenyl)methyl)piperazine
  • (R)-2-(3-Chloro-2-fluoro-5-(trifluoromethyl)phenyl)pyrrolidine
  • (1R,2S)-2-((Benzylamino)methyl)-1-(4-chloro-3-fluorophenyl)propane-1,3-diol ((1S,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonate
  • Methyl (6S,9S,12S)-12-((1H-imidazol-5-yl)methyl)-9-(3-(tert-butoxy)-3-oxopropyl)-2,2-dimethyl-6-(2-(methylthio)ethyl)-4,7,10-trioxo-3-oxa-5,8,11-triazatridecan-13-oate
  • (S)-3-Azaspiro[5.5]undecan-8-amine dihydrochloride
  • Methyl (S)-2-amino-3-(quinoxalin-2-yl)propanoate
  • (1S,3S,4R)-3-Hydroxy-7-azabicyclo[2.2.1]heptane-1-carboxylic acid hydrochloride
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