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1-Benzothiophene-3-carbaldehyde

Names

[ CAS No. ]:
5381-20-4

[ Name ]:
1-Benzothiophene-3-carbaldehyde

[Synonym ]:
1-benzothiophen-3-carbaldehyd
Benzo[b]thiophene-3-carboxaldehyde
3-Benzothiophenecarboaldehyde
MFCD00052376
3-Formylbenzo[b]thiophene
1-Benzothiophene-3-carbaldehyde
3-benzothiophene carbaldehyde
benzothiophene-3-carboxaldehyde
Benzo[b]thiophene-3-carbaldehyde
thianaphthene-3-carboxaldehyde
benzo<b>thiophene-3-carboxaldehyde

Biological Activity

[Description]:

Benzo[b]thiophene-3-carbaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
303.2±15.0 °C at 760 mmHg

[ Melting Point ]:
53-57 °C(lit.)

[ Molecular Formula ]:
C9H6OS

[ Molecular Weight ]:
162.21

[ Flash Point ]:
137.2±20.4 °C

[ Exact Mass ]:
162.013931

[ PSA ]:
45.31000

[ LogP ]:
3.80

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.720

MSDS

Safety Information

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

[ Hazard Codes ]:
Xi: Irritant;

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

Synthetic Route

Precursor & DownStream

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

Molecular modelling, synthesis, cytotoxicity and anti-tumour mechanisms of 2-aryl-6-substituted quinazolinones as dual-targeted anti-cancer agents.

Br. J. Pharmacol. 169(7) , 1574-86, (2013)

Our previous study demonstrated that 6-(pyrrolidin-1-yl)-2-(3-methoxyphenyl)quinazolin-4-one (HMJ38) was a potent anti-tubulin agent. Here, HMJ38 was used as a lead compound to develop more potent ant...

Benzo[b]thiophene derivatives. VIII. Benzo[b]thiophene-3-earboxaldehyde and derivatives. Campaigne E and Neiss ES.

J. Heterocycl. Chem. 3(1) , 46-50, (1966)

An efficient phosphine-free palladium coupling for the synthesis of new 2-arylbenzo[b]thiophenes. Chabert JFD, et al.

Tetrahedron 60(14) , 3221-3230, (2004)


More Articles


Related Compounds

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