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Merck
CN

257648

Ethyl 2-thiopheneacetate

98%

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About This Item

Empirical Formula (Hill Notation):
C8H10O2S
CAS Number:
Molecular Weight:
170.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
260-715-0
MDL number:
Assay:
98%
Form:
liquid
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InChI key

QSUANHXENVRFDN-UHFFFAOYSA-N

InChI

1S/C8H10O2S/c1-2-10-8(9)6-7-4-3-5-11-7/h3-5H,2,6H2,1H3

SMILES string

CCOC(=O)Cc1cccs1

assay

98%

form

liquid

refractive index

n20/D 1.51 (lit.)

bp

119-121 °C/23 mmHg (lit.)

density

1.134 g/mL at 25 °C (lit.)

functional group

ester

Application

Ethyl 2-thiopheneacetate has been used in preparation of:
  • S-(2-(5-((amidinothio)methyl)-2-thienyl)ethyl)isothiourea
  • pyrrolo [3,2-b] pyrrole-based copolymers for organic photovoltaic device

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

219.2 °F - closed cup

flash_point_c

104.00 °C - closed cup

ppe

Eyeshields, Gloves

Regulatory Information

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Pyrrolo [3, 2-b] pyrrole-Based Copolymers as Donor Materials for Organic Photovoltaics.
Song S, et al.
Bull. Korean Chem. Soc., 34(11), 3399-3399 (2013)
E P Garvey et al.
The Journal of biological chemistry, 269(43), 26669-26676 (1994-10-28)
S-Ethylisothiourea was a potent competitive inhibitor of human nitric oxide synthase (NOS), with Ki values of 17, 36, and 29 nM for the inducible (i), endothelial (e), and neuronal (n) isozymes, respectively. Unlike some potent inhibitors of NOS, no time

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