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Sigma-Aldrich

5-Bromo-2-thiophenecarboxaldehyde

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
EC Number:
225-176-8
MDL number:
MFCD00005432
UNSPSC Code:
12352100
PubChem Substance ID:
24849240
NACRES:
NA.22

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.)

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

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Application

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

210.2 °F - closed cup

Flash Point(C)

99.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
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
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

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