5-Bromo-2-thiophenecarbaldehyde

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Names

[ Name ]:
5-Bromo-2-thiophenecarbaldehyde

[Synonym ]:
5-Bromothiophene-2-carbaldehyde
5-Bromo-2-formylthiophene
2-Thiophenecarboxaldehyde, 5-bromo-
5-Bromothiophene-2-carboxaldehyde
5-bromo-2-thiophenecarboxaldehyde
5-Bromo-2-thiophenecarbaldehyde
5-Bromothenaldehyde
EINECS 225-176-8
MFCD00005432

Chemical & Physical Properties

[ Density]:
1.8±0.1 g/cm3

[ Boiling Point ]:
230.7±0.0 °C at 760 mmHg

[ Melting Point ]:
104-6ºC

[ Molecular Formula ]:
C₅H₃BrOS

[ Molecular Weight ]:
191.05

[ Flash Point ]:
98.9±0.0 °C

[ Exact Mass ]:
189.908783

[ PSA ]:
45.31000

[ LogP ]:
1.97

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.653

[ Storage condition ]:
0-6°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S36/37/39-S26-S22

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2934999090

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

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

ACS Appl. Mater. Interfaces 6(18) , 15774-82, (2014)

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-withdr...

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

Int. J. Rad. Appl. Instrum. B 16(7) , 681-6, (1989)

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 th...

5-Bromo-2-ethyl-3-thiophenecarbaldehyde
5-Bromo-3-methyl-2-thiophenecarbaldehyde
5-bromo-2-(4-bromophenyl)-1-benzofuran
5-BROMO-2,3-DIHYDRO-1-METHYL-1H-ISOINDOLE HYDROCHLORIDE
(5-BROMO-2-HYDROXY-4-METHOXYPHENYL)(PHENYL)METHANONE
5-Bromo-2-chloro-N-[3-(trifluoromethyl)phenyl]-4-pyrimidinamine
1-{[1-(2-fluorophenyl)-5-pyridin-2-yl-1H-1,2,3-triazol-4-yl]carbonyl}indoline
2-(4-{[1-(2-fluorophenyl)-5-pyridin-2-yl-1H-1,2,3-triazol-4-yl]carbonyl}piperazin-1-yl)pyrimidine
ethyl 3-({[1-(2-fluorophenyl)-5-pyridin-2-yl-1H-1,2,3-triazol-4-yl]carbonyl}amino)benzoate
N-(2-(2,3-dihydrobenzofuran-5-yl)-2-(dimethylamino)ethyl)-7-methoxybenzofuran-2-carboxamide
2-Methoxy-4-methyl-5-nitrobenzamide
(E)-N-(2-(2,3-dihydrobenzofuran-5-yl)-2-(dimethylamino)ethyl)-3-(thiophen-3-yl)acrylamide
N-(2-(2,3-dihydrobenzofuran-5-yl)-2-(dimethylamino)ethyl)-3-(4-fluorophenyl)-1-methyl-1H-pyrazole-5-carboxamide
N-(2-(2,3-dihydrobenzofuran-5-yl)-2-(dimethylamino)ethyl)furan-3-carboxamide
5-chloro-N-(2-(2,3-dihydrobenzofuran-5-yl)-2-(dimethylamino)ethyl)-2-methylbenzenesulfonamide
1-(2-Chlorophenyl)-N-[2-(2,3-dihydro-1-benzofuran-5-YL)-2-(dimethylamino)ethyl]methanesulfonamide

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