ChemicalBook--->CAS DataBase List--->4156-16-5

4156-16-5

4156-16-5 Structure

4156-16-5 Structure
IdentificationMore
[Name]

2-Ethyl-5-phenylisoxazolium-3'-sulfonate
[CAS]

4156-16-5
[Synonyms]

2-ETHYL-5-PHENYLISOXAZOLIUM-3'-SULFONATE
2-ETHYL-5-PHENYLISOXAZOLIUM-3'-SULPHONATE
3-(2-ETHYL-5-ISOXAZOLIO)BENZENESULFONATE
NEPIS
N-ETHYL-5-PHENYLISOXAZOLIUM-3'-SULFONATE
WOODWARDS REAGENT K
WOODWARD'S REAGENT K
3-(2-Ethyl-5-isoxazolio)benzenesulphonate~NEPIS~Woodwards
2-ETHYL-5-PHENYLISOXAZOLIUM-3'-SULPHONEATE
Isoxazolium, 2-ethyl-5-(3-sulfophenyl)-, inner salt
NEPIS 2-ETHYL-5-PHENYLISOXAZOLIUM-3''-SULFONATE
3-(2-ETHYL-5-ISOXAZOLIO)BENZENESULFONATE 99+%
2-Ethyl-5-phenylisoxazolium-3μ-sulfonate, NEPIS
5-(3-Sulfonatophenyl)-2-ethylisoxazol-2-ium
[EINECS(EC#)]

223-988-7
[Molecular Formula]

C11H11NO4S
[MDL Number]

MFCD00012128
[Molecular Weight]

253.27
[MOL File]

4156-16-5.mol
Chemical PropertiesBack Directory
[Appearance]

white to off-white crystalline powder
[Melting point ]

216-219 °C (dec.)
[density ]

1.3854 (rough estimate)
[refractive index ]

1.4790 (estimate)
[storage temp. ]

Store at RT.
[solubility ]

insol MeCN, MeNO2, DMF, CH2Cl2; sol H2O.
[Merck ]

10050
[BRN ]

4149224
[Major Application]

peptide synthesis
[InChI]

1S/C11H11NO4S/c1-2-12-7-6-11(16-12)9-4-3-5-10(8-9)17(13,14)15/h3-8H,2H2,1H3
[InChIKey]

MWOOKDULMBMMPN-UHFFFAOYSA-N
[SMILES]

CC[n+]1ccc(o1)-c2cccc(c2)S([O-])(=O)=O
[CAS DataBase Reference]

4156-16-5(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

white to off-white crystalline powder
[Uses]

Peptide-bond former.
[Application]

2-Ethyl-5-phenylisoxazolium-3'-sulfonate is a coupling agent for peptide synthesis; protein modification; and reduction of carboxylic acids to alcohols.
[reaction suitability]

reaction type: Coupling Reactions
[storage]

Stable to light and temperature and nonhygroscopic. No extra precautions  need to be observed.
[Purification Methods]

Crystallise the reagent from diethyl ether or ethyl acetate/pet ether. [Lamas et al. J Am Chem Soc 108 5543 1986.] It is best purified by dissolving in excess of aqueous N HCl and precipitating with Me2CO to give a white fluffy solid. [Woodward et al. Tetrahedron 22 Suppl 8 321 1966, Fieser & Fieser Reagents for Organic Synthesis 1 385, 2 198.]
Spectrum DetailBack Directory
[Spectrum Detail]

2-Ethyl-5-phenylisoxazolium-3'-sulfonate(4156-16-5)1HNMR
2-Ethyl-5-phenylisoxazolium-3'-sulfonate(4156-16-5)IR1
2-Ethyl-5-phenylisoxazolium-3'-sulfonate(4156-16-5)Raman
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

4156-16-5(sigmaaldrich)
[TCI AMERICA]

N-Ethyl-5-phenylisoxazolium-3'-sulfonate,>98.0%(T)(4156-16-5)
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