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About This Item
Empirical Formula (Hill Notation):
C8H10OS
CAS Number:
Molecular Weight:
154.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
liquid
assay:
99%
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Quality Level
assay
99%
form
liquid
refractive index
n20/D 1.544 (lit.)
bp
105-108 °C/15 mmHg (lit.)
density
1.086 g/mL at 25 °C (lit.)
functional group
ketone
SMILES string
CC(=O)c1cc(C)sc1C
InChI
1S/C8H10OS/c1-5-4-8(6(2)9)7(3)10-5/h4H,1-3H3
InChI key
PUSJAEJRDNPYKM-UHFFFAOYSA-N
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Application
3-Acetyl-2,5-dimethylthiophene was used in the synthesis of heterocyclic ketimines, 3-acetyl-2,5-dimethylthiophene thiosemicarbazone and 3-acetyl-2,5- dimethylthiophene semicarbazone.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
210.2 °F - closed cup
flash_point_c
99 °C - closed cup
ppe
Eyeshields, Gloves
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Krishna Sharma et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(1), 422-427 (2009-12-08)
Reactions of 3-acetyl-2,5-dimethylthiophene with thiosemicarbazide and semicarbazide hydrochloride resulted in the formation of new heterocyclic ketimines, 3-acetyl-2,5-dimethylthiophene thiosemicarbazone (C(9)H(13)N(3)OS(2) or L(1)H) and 3-acetyl-2,5- dimethylthiophene semicarbazone (C(9)H(13)N(3)OS or L(2)H), respectively. The Pd(II) and Pt(II) complexes have been synthesized by mixing metal
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