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257648

Ethyl 2-thiopheneacetate

Name: Ethyl 2-thiopheneacetate
Brand: ALDRICH

98%

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About This Item

Empirical Formula (Hill Notation):

C₈H₁₀O₂S

CAS Number:

57382-97-5

Molecular Weight:

170.23

NACRES:

NA.22

PubChem Substance ID:

24855600

UNSPSC Code:

12352100

EC Number:

260-715-0

MDL number:

MFCD00005457

Assay:

98%

Form:

liquid

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Properties

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

SMILES string

CCOC(=O)Cc1cccs1

InChI

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

InChI key

QSUANHXENVRFDN-UHFFFAOYSA-N

Description

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)

Potent and selective inhibition of human nitric oxide synthases. Inhibition by non-amino acid isothioureas.

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

Global Trade Item Number

SKU	GTIN
257648-25G	04061837836817