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Merck
CN

225797

3-Acetyl-2,5-dimethylthiophene

99%

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About This Item

Empirical Formula (Hill Notation):
C8H10OS
CAS Number:
Molecular Weight:
154.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
219-779-5
MDL number:
Assay:
99%
Form:
liquid
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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

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

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



Global Trade Item Number

SKUGTIN
225797-10G04061837836626