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3-Thiophenecarboxaldehyde

Names

[ CAS No. ]:
498-62-4

[ Name ]:
3-Thiophenecarboxaldehyde

[Synonym ]:
3-FORMYLTHIOPHENE
3-Thiophenealdehyde
3-Thiophenecarboxaldehyde
Thiophen-3-carbaldehyd
Thiophene-3-carboxaldehyde
EINECS 207-865-5
3-Thiophenecarbaldehyde
thiophene-3-carbaldehyde
3-Thiophenaldehyde
MFCD00005466
3-THIOPHENE CARBOXALDEHYDE

Chemical & Physical Properties

[ Density]:
1.28

[ Boiling Point ]:
194-196 ºC

[ Melting Point ]:
-30 °C

[ Molecular Formula ]:
C5H4OS

[ Molecular Weight ]:
112.150

[ Flash Point ]:
64 ºC

[ Exact Mass ]:
111.998283

[ PSA ]:
45.31000

[ LogP ]:
1.01

[ Vapour Pressure ]:
0.5±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.610

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R22;R43

[ Safety Phrases ]:
S37-S24

[ RIDADR ]:
1989.0

[ WGK Germany ]:
3

[ Hazard Class ]:
3.0

[ 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

Synthesis and structure-activity relationships among glycosidic derivatives of 4'-demethylepipodophyllotoxin and epipodophyllotoxin, showing VM26- and VP16-213-like activities.

Anticancer Drug Des. 2(1) , 1-12, (1987)

We have synthesized acetal and ketal derivatives of 4'-demethylepipodophyllotoxin-beta-D-glucoside (DMEPG) and epipodophyllotoxin-beta-D-glucoside (EPG) with a number of different aldehydes (viz. acet...

Synthesis and carbonic anhydrase inhibitory activity of 4-substituted 2-thiophenesulfonamides.

J. Med. Chem. 37(11) , 1646-51, (1994)

A series of 4-substituted 2-thiophenesulfonamides was prepared from 3-thiophenecarboxaldehyde using metalation chemistry developed for 3-furaldehyde. Several of these compounds inhibit carbonic anhydr...

1, 2-Di-3-thienyl-2-hydroxyethanone (3, 3′-thenoin). Crundwell G, et al.

Acta Crystallogr. Sect. E Struct. Rep. Online 58(6) , o668-o670, (2002)


More Articles


Related Compounds