144193
4,6-Dichloro-2-methylthio-5-phenylpyrimidine
95%
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Empirical Formula (Hill Notation):
C11H8Cl2N2S
CAS Number:
Molecular Weight:
271.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
95%
mp
107-111 °C (lit.)
SMILES string
CSc1nc(Cl)c(c(Cl)n1)-c2ccccc2
InChI
1S/C11H8Cl2N2S/c1-16-11-14-9(12)8(10(13)15-11)7-5-3-2-4-6-7/h2-6H,1H3
InChI key
LMTMZMBTPXASSW-UHFFFAOYSA-N
Application
4,6-Dichloro-2-methylthio-5-phenylpyrimidine was used in the synthesis of cinchona alkaloid-derived catalysts.
Biochem/physiol Actions
4,6-Dichloro-2-methylthio-5-phenylpyrimidine has significant in vivo antinflammatory activity.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Michael A Calter et al.
Organic letters, 13(23), 6328-6330 (2011-11-08)
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.
Letters in Drug Design & Discovery, 7(6), 438-445 (2010)
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