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301922

Sigma-Aldrich

2-Acetamido-4-methylthiazole

98%

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About This Item

Empirical Formula (Hill Notation):
C6H8N2OS
CAS Number:
Molecular Weight:
156.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
solid
assay:
98%

Quality Level

assay

98%

form

solid

mp

134-136 °C (lit.)

functional group

amide

SMILES string

CC(=O)Nc1nc(C)cs1

InChI

1S/C6H8N2OS/c1-4-3-10-6(7-4)8-5(2)9/h3H,1-2H3,(H,7,8,9)

InChI key

DPDJXTANWGNJOE-UHFFFAOYSA-N

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General description

The metabolism of 2-acetamido-4-methylthiazole in rat has been studied.[1] Sulfonation of 2-acetamido-4-methylthiazole by chlorosulfonic acid has been reported.[2]

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signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Notes-2-Aminothiazolesulfonamides.
Ziegler C, et al.
The Journal of Organic Chemistry, 25(8), 1454-1455 (1960)
D H Chatfield et al.
The Biochemical journal, 134(4), 869-878 (1973-08-01)
The metabolism of some anti-inflammatory acetamidothiazoles was studied in the rat. The main metabolites were the corresponding acetylthiohydantoic acids, produced by fission of the thiazole ring. Minor metabolites arising from oxidation of the methyl or phenyl substituents were also identified.

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