2-Bromothiophene-5-Sulfonamide

Modify Date: 2024-01-02 08:14:15

2-Bromothiophene-5-Sulfonamide Structure
2-Bromothiophene-5-Sulfonamide structure
Common Name 2-Bromothiophene-5-Sulfonamide
CAS Number 53595-65-6 Molecular Weight 242.114
Density 2.0±0.1 g/cm3 Boiling Point 386.4±52.0 °C at 760 mmHg
Molecular Formula C4H4BrNO2S2 Melting Point 138-142 °C(lit.)
MSDS Chinese USA Flash Point 187.5±30.7 °C

 Names

Name 5-Bromothiophene-2-sulfonamide
Synonym More Synonyms

 Chemical & Physical Properties

Density 2.0±0.1 g/cm3
Boiling Point 386.4±52.0 °C at 760 mmHg
Melting Point 138-142 °C(lit.)
Molecular Formula C4H4BrNO2S2
Molecular Weight 242.114
Flash Point 187.5±30.7 °C
Exact Mass 240.886673
PSA 96.78000
LogP 1.03
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.647

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi:Irritant;
Risk Phrases R36/37/38
Safety Phrases S26-S37/39
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2935009090

 Customs

HS Code 2935009090
Summary 2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%

 Articles5

More Articles
Synthesis, Density Functional Theory (DFT), Urease Inhibition and Antimicrobial Activities of 5-Aryl Thiophenes Bearing Sulphonylacetamide Moieties.

Molecules 20 , 19914-28, (2015)

A variety of novel 5-aryl thiophenes 4a-g containing sulphonylacetamide (sulfacetamide) groups were synthesized in appreciable yields via Pd[0] Suzuki cross coupling reactions. The structures of these...

Cerebrovasodilatation through selective inhibition of the enzyme carbonic anhydrase. 3. 5-(Arylthio)-, 5-(arylsulfinyl)-, and 5-(arylsulfonyl)thiophene-2-sulfonamides.

J. Med. Chem. 24(8) , 959-64, (1981)

A series of 5-(arylthio)-, 5-(arylsulfinyl)-, and 5-(arylsulfonyl)thiophene-2-sulfonamides is described and anticonvulsant activities are listed for the compounds. In most cases, the sulfones had the ...

Acyl sulfonamide anti-proliferatives. Part 2: activity of heterocyclic sulfonamide derivatives.

Bioorg. Med. Chem. Lett. 15(3) , 617-20, (2005)

The anti-proliferative activity of acylated heterocyclic sulfonamides is described in Vascular Endothelial Growth Factor-dependent Human Umbilical Vascular Endothelial Cells (VEGF-HUVEC) and in HCT116...

 Synonyms

5-Bromothiophene-2-sulfonamide
MFCD00067990
5-Bromo-thiophene-2-sulfonic acid amide
2-Thiophenesulfonamide, 5-bromo-
5-Bromo-2-thiophenesulfonamide
2-Bromothiophene-5-Sulfonamide
2-bromo thiophene-5-sulfonamide