Passa al contenuto
Merck
Tutte le immagini(3)

Documenti

402869

Sigma-Aldrich

Chloramine T trihydrate

ACS reagent, 98%

Sinonimo/i:

N-Chloro-p-toluenesulfonamide sodium salt

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(3)

About This Item

Formula condensata:
CH3C6H4SO2NClNa · 3H2O
Numero CAS:
7080-50-4
Peso molecolare:
281.69
Beilstein:
3924168
Numero CE:
204-854-7
Numero MDL:
MFCD00149066
Codice UNSPSC:
12352100
ID PubChem:
24865128
NACRES:
NA.21

Grado

ACS reagent

Livello qualitativo

200

Saggio

98%
98.0-103.0% (ACS specification)

Forma fisica

powder

Impiego in reazioni chimiche

reagent type: oxidant

Impurezze

<1.5% insolubles (alcohol)

pH

8.0-10.0 (25 °C, 5%)

Punto di fusione

167-170 °C (lit.)

Solubilità

H2O: passes test

Compatibilità

passes test for determination of bromide

Stringa SMILE

O.O.O.Cc1ccc(cc1)S(=O)(=O)N([Na])Cl

InChI

1S/C7H7ClNO2S.Na.3H2O/c1-6-2-4-7(5-3-6)12(10,11)9-8;;;;/h2-5H,1H3;;3*1H2/q-1;+1;;;
NZYOAGBNMCVQIV-UHFFFAOYSA-N

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Descrizione generale

Chloramine T (CAT) trihydrate is a commonly used reagent for organic synthesis especially in heterocyclic chemistry. CAT is an active chlorine compound that shows antimicrobial activity.

Applicazioni

Chloramine T trihydrate may be used as an oxidizing agent in the synthesis of 8-chloro-[1,2,4]triazolo[4,3-a]pyrazine derivatives and novel isoxazolines.
It may also be used in the synthesis of the following compounds:
  • Nitrile imines by the oxidative dehydrogenation of N-(nitrobenzyl)-imidazole aldehyde hydrazine.
  • Mono-N-tosylated-1,2-diamines.
  • 3,5-Disubstituted isoxazoles.
  • Fused 3,6-disubstituted triazolothiadiazoles by the oxidative cyclization of N-heteroaryl-substituted hydrazones.
Nitrene source for aziridinations and aminohydroxylations.

Confezionamento

Capable of oxidative cyclization to produce various heterocycles.

Avvertenze

Danger

Indicazioni di pericolo

H302,H314,H334

Classi di pericolo

Acute Tox. 4 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B

Rischi supp

EUH031

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

377.6 °F - closed cup

Punto d’infiammabilità (°C)

192 °C - closed cup

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
STBK7802
STBK6340
STBK3526
STBK1659
STBK0022

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

Facile one pot synthesis of 8-chloro-[1, 2, 4] triazolo [4, 3-a] pyrazines via oxidative cyclisation using chloramine T.
Mal S, et al.
Tetrahedron Letters, 56(22), 2896-2901 (2015)
M Nagl et al.
The British journal of dermatology, 149(3), 590-597 (2003-09-27)
The well-known active chlorine compound chloramine T (CAT) with broad-spectrum antimicrobial activity is in common therapeutic use for leg ulcers with purulent coatings; however, this treatment is painful. The tolerability of the less aggressive N-chlorotaurine (NCT), an endogenous compound also
[1-(4-Nitrobenzyl)-2-butyl-4-chloro-1H-imidazol-5-yl]-4, 5-dihydro-1-phenyl-1H-pyrazole: Synthesis, Anti-Inflammatory and Analgesic Activities.
Sreenivasa S and Shankar BJ.
Open Journal of Medicinal Chemistry, 3(2) (2013)
Synthesis and antimicrobial activity of novel isoxazolines by 1, 3-dipolar cycloaddition reactions.
Govindaraju M, et al.
International Journal of ChemTech Research, 6(2), 886-890 (2014)
Novel (+)-3-Carene Derivatives and Their Application in Asymmetric Synthesis.
Roszkowski P, et al.
Synthesis, 47(04), 569-574 (2015)
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.