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152625

5-Bromo-2-thiophenecarboxaldehyde

Name: 5-Bromo-2-thiophenecarboxaldehyde
Brand: ALDRICH

95%

Synonym(s):

5-Bromothenaldehyde

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About This Item

Empirical Formula (Hill Notation):

C₅H₃BrOS

CAS Number:

4701-17-1

Molecular Weight:

191.05

NACRES:

NA.22

PubChem Substance ID:

24849240

UNSPSC Code:

12352100

EC Number:

225-176-8

MDL number:

MFCD00005432

Assay:

95%

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Properties

Quality Level

100

assay

95%

refractive index

n20/D 1.637 (lit.)

bp

105-107 °C/11 mmHg (lit.)

density

1.607 g/mL at 25 °C (lit.)

functional group

aldehyde, bromo

storage temp.

2-8°C

SMILES string

[H]C(=O)c1ccc(Br)s1

InChI

1S/C5H3BrOS/c6-5-2-1-4(3-7)8-5/h1-3H

InChI key

GFBVUFQNHLUCPX-UHFFFAOYSA-N

Description

Application

5-Bromo-2-thiophenecarboxaldehyde was used to prepare 5-[18F]fluoro-2-2-thiophene carboxaldehyde.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

210.2 °F - closed cup

flash_point_c

99.00 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Thiophenes as phenyl bio-isosteres: application in radiopharmaceutical design--I. Dopamine uptake antagonists.

M R Kilbourn

International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology, 16(7), 681-686 (1989-01-01)

Possible applications of thiophenes in radiopharmaceutical chemistry have been explored. Thiophene for benzene ring substitution was applied to the synthesis of thienyl-[18F]GBR 13119, an analog of the potent and selective dopamine uptake inhibitor [18F]GBR 13119. In vivo regional brain distribution

Synthesis and Spectral Identification of Three Schiff Bases with a 2-(Piperazin-1-yl)-N-(thiophen-2-yl methylene)ethanamine Moiety Acting as Novel Pancreatic Lipase Inhibitors: Thermal, DFT, Antioxidant, Antibacterial, and Molecular Docking Investigations.

Ismail Warad et al.

Molecules (Basel, Switzerland), 25(9) (2020-05-15)

Three new tetradentate NNNS Schiff bases (L1-L3) derived from 2-(piperidin-4-yl)ethanamine were prepared in high yields. UV-Visible and FTIR spectroscopy were used to monitor the dehydration reaction between 2-(piperidin-4-yl)ethanamine and the corresponding aldehydes. Structures of the derived Schiff bases were deduced

Effects of cyano-substituents on the molecular packing structures of conjugated polymers for bulk-heterojunction solar cells.

Hyojung Cha et al.

ACS applied materials & interfaces, 6(18), 15774-15782 (2014-08-26)

The molecular packing structures of two conjugated polymers based on alkoxy naphthalene, one with cyano-substituents and one without, have been investigated to determine the effects of electron-withdrawing cyano-groups on the performance of bulk-heterojunction solar cells. The substituted cyano-groups facilitate the

Global Trade Item Number

SKU	GTIN
Y0001004	04061833796719
195510-1G	04061825970141
152625-25G	04061838740441
152625-100G	04061838740434