4,6-dichloro-2-methylsulfanyl-5-phenylpyrimidine

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Names

[ CAS No. ]:
64415-11-8

[ Name ]:
4,6-dichloro-2-methylsulfanyl-5-phenylpyrimidine

[Synonym ]:
LMTMZMBTPXASSW-UHFFFAOYSA
4,6-Dichlor-2-methylmercapto-5-phenyl-pyrimidin
MFCD00006084
4,6-dichloro-2-methylsulfanyl-5-phenyl-pyrimidine
4,6-Dichloro-2-methylthio-5-phenylpyrimidine
4,6-Dichloro-5-phenyl-2-methylthiopyrimidine
EINECS 264-877-3

Chemical & Physical Properties

[ Density]:
1.43g/cm3

[ Boiling Point ]:
364.3ºC at 760 mmHg

[ Melting Point ]:
107-111ºC(lit.)

[ Molecular Formula ]:
C11H8Cl2N2S

[ Molecular Weight ]:
271.16600

[ Flash Point ]:
174.1ºC

[ Exact Mass ]:
269.97900

[ PSA ]:
51.08000

[ LogP ]:
4.17230

[ Index of Refraction ]:
1.657

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
26-27-28-36/37/39-45

[ RIDADR ]:
UN 3263 8/PG 2

[ Packaging Group ]:
III

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • methyl thiocyanate
  • 2-phenylpropanedioyl dichloride

DownStream

Articles

Catalytic, asymmetric, interrupted Feist-Bénary reactions of α-tosyloxyacetophenones.

Org. Lett. 13(23) , 6328-30, (2011)

A new variant of the Interrupted Feist-Bénary (IFB) reaction uses α-tosyloxyacetophenones as electrophiles and proceeds in good yields and excellent enantioselectivities.

Application of molecular topology to the search of novel NSAIDs: experimental validation of activity. Galvez-Llompart M, et al.

Lett. Drug Des. Discov. 7(6) , 438-445, (2010)


More Articles

Related Compounds

  • 4,6-dichloro-2-methylsulfanyl-5-(2,4,6-trifluorophenyl)pyrimidine
  • 4,6-Dichloro-2-(methylsulfanyl)-5-nitropyrimidine
  • [4,6-Dichloro-2-(methylsulfanyl)-5-pyrimidinyl]methanol
  • Methyl 4,6-dichloro-2-(methylthio)pyrimidine-5-carboxylate
  • 4,6-dichloro-2-isocyanato-5-phenylpyrimidine
  • 4,6-Dichloro-2-(methylthio)pyrimidine-5-carbonitrile
  • 1-(6-Chloropyrimidin-4-yl)-4-methyl-1,4-diazepane
  • [(4-Methoxypiperidin-4-yl)methyl](methyl)amine
  • 1-(Trifluoroacetyl)-decahydroquinoline-2-carboxylic acid
  • [(3-Ethoxypyrrolidin-3-yl)methyl](methyl)amine
  • 1-(2H-tetrazol-5-yl)propan-2-amine
  • N-methyl-N-[2-(1-methylpyrrolidin-2-yl)ethyl]hydroxylamine
  • methyl S-(4-fluorophenyl)cysteinate
  • N-methyl-N-[(1-methylpiperidin-2-yl)methyl]hydroxylamine
  • N1-[1-(2,4-Dimethyl-5-thiazolyl)ethyl]-1,3-butanediamine
  • 3-(2-Aminopropan-2-yl)-1-methylpyrrolidin-3-ol
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