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Merck
CN

W503509

2-Acetylthiophene

≥98%, FG

Synonym(s):

Methyl-2-thienyl ketone

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About This Item

Empirical Formula (Hill Notation):
C6H6OS
CAS Number:
88-15-3
Molecular Weight:
126.18
NACRES:
NA.21
Flavis number:
15.040
PubChem Substance ID:
24902014
UNSPSC Code:
12164502
EC Number:
201-804-6
MDL number:
MFCD00005442
Beilstein/REAXYS Number:
107910

Key Documents

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Product Name

2-Acetylthiophene, ≥98%, FG

InChI

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

InChI key

WYJOVVXUZNRJQY-UHFFFAOYSA-N

SMILES string

CC(=O)c1cccs1

biological source

synthetic

grade

FG
Fragrance grade
Halal
Kosher

agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002

assay

≥98%

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.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

sulfurous

Quality Level

400

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pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

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

Storage Class

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

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SHBQ3677
SHBP5326
SHBL4208
MKCG2094
MKCB4655

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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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