n-ethyl-5-phenylisoxazolium-3'-sulfonate

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Names

[ CAS No. ]:
4156-16-5

[ Name ]:
n-ethyl-5-phenylisoxazolium-3'-sulfonate

[Synonym ]:
EINECS 223-988-7
3-(2-Ethyl-1,2-oxazol-2-ium-5-yl)benzenesulfonate
2-Ethyl-5-phenylisoxazolium-3'-sulfonate
2-Ethyl-5-phenylisoxazolium-3'-sulphoneate
Isoxazolium, 2-ethyl-5-(3-sulfophenyl)-, inner salt
NEPIS
n-ethyl-5-phenylisoxazolium-3'-sulfonate
Woodwards reagent K
2-ethyl-5-phenylisoxazolium-3'-sulphonate
3-(2-ethylisoxazol-5-yl)benzenesulfonic acid
2-ethyl-5-(3-sulfo-phenyl)-isoxazolium,betaine
N-ethyl-5-phenylisoxazolium-3'-sulphonate
2-Ethyl-5-m-sulfophenylisoxazolium Hydroxide Inner Salt
MFCD00012128
Woodward's reagent potassium

Chemical & Physical Properties

[ Melting Point ]:
216-219 °C (dec.)

[ Molecular Formula ]:
C11H11NO4S

[ Molecular Weight ]:
253.274

[ Exact Mass ]:
253.040878

[ PSA ]:
82.60000

[ LogP ]:
2.23890

[ Storage condition ]:
Store at RT.

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
22

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

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

[Synthesis of electroconductive polyaniline using immobilized laccase].

Prikl. Biokhim. Mikrobiol. 45(1) , 33-7, (2009)

A new method for synthesis of the conductive complex between polyaniline (PANI) and poly(2-acrylamido-2-methyl-1-propanosulfonic acid) (PAMPS) was proposed; in this method, the immobilized laccase fro...

The carboxyl side chain of glutamate 681 interacts with a chloride binding modifier site that allosterically modulates the dimeric conformational state of band 3 (AE1). Implications for the mechanism of anion/proton cotransport.

Biochemistry 42(6) , 1589-602, (2003)

Glutamate 681 is thought to be located within the transport channel of band 3 (AE1, the chloride/bicarbonate exchanger), where it acts as a proton donor for the anion/proton cotransport function. Here...

Effect of protein-modifying reagents on ecto-apyrase from rat brain.

Int. J. Biochem. Cell Biol. 32(1) , 105-13, (2000)

We have tested several chemical modifiers to investigate which amino acid residues, present in the primary structure of the ecto-apyrase, could be involved in catalysis. Synaptosomes from cerebral cor...


More Articles


Related Compounds

  • 4-[(1-ethyl-2-oxo-3,4-dihydroquinolin-5-yl)oxy]butanenitrile
  • Isoxazolium, 2-ethyl-5-phenyl-, tetrafluoroborate(1-)
  • N-ethyl-5,6-dimethylbenzo[c]acridine-7-carboxamide
  • N-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)pyridin-2-amine
  • N-ethyl-5-(4-methylpiperazin-1-yl)-11H-dibenzo[1,2-a:1',2'-d][7]annulen-11-amine
  • N-ethyl-5-methyl-3,6-diphenylpyridazin-4-amine
  • N-(4-fluorophenyl)-3-methyl-4-oxo-1-(p-tolyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxamide
  • N-(3-chlorophenyl)-3-methyl-4-oxo-1-(p-tolyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxamide
  • N-(4-bromophenyl)-3-methyl-4-oxo-1-(p-tolyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxamide
  • N-(2-ethoxyphenyl)-3-methyl-4-oxo-1-(p-tolyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxamide
  • N-(4-ethoxyphenyl)-3-methyl-4-oxo-1-(p-tolyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxamide
  • 3-methyl-4-oxo-1-(p-tolyl)-N-(4-(trifluoromethoxy)phenyl)-4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxamide
  • N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenyl)-2-(ethylsulfonyl)benzamide
  • N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenyl)-3-(ethylsulfonyl)benzamide
  • N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenyl)-4-(ethylsulfonyl)benzamide
  • ethyl N-[(2E)-2-{[(5-iodopyridin-2-yl)amino]methylidene}-3-oxobutanoyl]carbamate
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