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144193

Sigma-Aldrich

4,6-Dichloro-2-methylthio-5-phenylpyrimidine

95%

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About This Item

Empirical Formula (Hill Notation):
C11H8Cl2N2S
CAS Number:
64415-11-8
Molecular Weight:
271.17
EC Number:
264-877-3
MDL number:
MFCD00006084
UNSPSC Code:
12352100
PubChem Substance ID:
24848640
NACRES:
NA.22
assay:
95%

assay

95%

mp

107-111 °C (lit.)

functional group

chloro
phenyl
thioether

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[1].

Biochem/physiol Actions

4,6-Dichloro-2-methylthio-5-phenylpyrimidine has significant in vivo antinflammatory activity[2].

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H314,H335

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
MKBN8299V
00116LN
20621BB

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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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