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Key Documents

Safety Information

A22602

Sigma-Aldrich

2-Acetylthiophene

98%

Synonym(s):

Methyl-2-thienyl ketone

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About This Item

Empirical Formula (Hill Notation):
C6H6OS
CAS Number:
Molecular Weight:
126.18
Beilstein:
107910
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.565 (lit.)

bp

214 °C (lit.)

mp

10-11 °C (lit.)

density

1.168 g/mL at 25 °C (lit.)

SMILES string

CC(=O)c1cccs1

InChI

1S/C6H6OS/c1-5(7)6-3-2-4-8-6/h2-4H,1H3

InChI key

WYJOVVXUZNRJQY-UHFFFAOYSA-N

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Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Acute Tox. 3 Dermal

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

206.6 °F

Flash Point(C)

97 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

A22602-100G:
A22602-BULK:
A22602-25ML:
A22602-100ML:
A22602-VAR:
A22602-25G:


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Jinbing Liu et al.
Bioorganic & medicinal chemistry, 16(3), 1096-1102 (2008-03-08)
A series of 1-(1-arylethylidene)thiosemicarbazide compounds and their analogues were synthesized and characterized by 1H NMR, MS. Their tyrosinase inhibitory activities were investigated by an assay based on the catalyzing ability of tyrosinase for the oxidation of L-DOPA, comparing with 4-methoxycinnamic
Mostafa M Ghorab et al.
Acta pharmaceutica (Zagreb, Croatia), 64(4), 419-431 (2014-12-23)
A novel series of thiophenes having biologically active sulfonamide 2-11, 3-methylisoxazole 12, 4-methoxybenzo[d] thiazole 13, quinoline 14, 15, benzoylphenylamino 16, and anthracene-9,10-dione 17 moieties were prepared. Structures of the newly synthesized compounds were established by elemental analysis and spectral data.

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