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C95501

Sigma-Aldrich

Cyanuric chloride

99%

Sinonimo/i:

2,4,6-Trichloro-1,3,5-triazine

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About This Item

Formula empirica (notazione di Hill):
C3Cl3N3
Numero CAS:
108-77-0
Peso molecolare:
184.41
Beilstein:
124246
Numero CE:
203-614-9
Numero MDL:
MFCD00006046
Codice UNSPSC:
12352101
ID PubChem:
24893171
NACRES:
NA.22

Densità del vapore

6.36 (vs air)

Livello qualitativo

200

Tensione di vapore

0.8 mmHg ( 62.2 °C)

Saggio

99%

Forma fisica

powder

P. eboll.

190 °C (lit.)

Punto di fusione

145-147 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

Clc1nc(Cl)nc(Cl)n1

InChI

1S/C3Cl3N3/c4-1-7-2(5)9-3(6)8-1
MGNCLNQXLYJVJD-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

Cyanuric chloride can be used as a reagent:   
  • In the preparation of acyl azides from carboxylic acids and sodium azide.       
  • For the conversion of carboxylic acids, N-Boc, N-Cbz, and N-Fmoc amino acids into corresponding alcohols.      
  • For the conversion of alcohols into the corresponding carbonyl compounds by alternative Swern oxidation reaction.


It can also be employed as a catalyst in the Beckmann rearrangement of ketoximes into amides in the presence of ZnCl2.
Reagent for the conversion of alcohols to chlorides and for the immobilization of microorganisms and enzymes.

Pittogrammi

CorrosionSkull and crossbones
GHS05,GHS06

Avvertenze

Danger

Indicazioni di pericolo

H302 - H314 - H317 - H330 - H335

Classi di pericolo

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A - STOT SE 3

Organi bersaglio

Respiratory system

Rischi supp

EUH014

Codice della classe di stoccaggio

6.1B - Non-combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

392.0 °F - closed cup

Punto d’infiammabilità (°C)

> 200 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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N-Phenylethylenediamine 98%

Sigma-Aldrich

P24152

N-Phenylethylenediamine

2,4,6-Tris(trifluoromethyl)-1,3,5-triazine 97%

Sigma-Aldrich

443980

2,4,6-Tris(trifluoromethyl)-1,3,5-triazine

J. Mol. Catal., 80, 269-269 (1993)
Xue Jiang et al.
Bioresource technology, 104, 473-479 (2011-11-25)
The influence of introduction of cyanuric chloride on glucose's yield (Y) in acid-catalyzed hydrolysis of microcrystalline cellulose (MCC) has been studied. The content of cyanuric chloride (C) in modified MCCs was determined by X-ray photoelectric spectroscopy. The chemical structures of
Chao Gao et al.
Chemical communications (Cambridge, England), 49(11), 1127-1129 (2013-01-04)
A series of novel triazinonide-bridged bisimidazolium pincers were easily synthesized by quaternization of functionalized N-phenylimidazoles with highly reactive cyanuric chloride under mild conditions. The pincer was proven to be a very efficient ligand for in situ Pd-catalyzed Suzuki-Miyaura reaction with
Ravi Bhushan et al.
Amino acids, 42(4), 1371-1378 (2011-01-20)
Six dichloro-s-triazine (DCT) reagents having L-Leu, D-Phg, L-Val, L-Met, L-Ala and L-Met-NH(2) as chiral auxiliaries in cyanuric chloride were introduced for enantioseparation of 13 proteinogenic amino acids. Four other DCTs and six monochloro-s-triazine (MCT) reagents having amino acid amides as
Ravi Bhushan et al.
Journal of chromatography. A, 1217(41), 6382-6387 (2010-09-08)
Four dichloro-s-triazine (DCT) and five monochloro-s-triazine (MCT) chiral derivatizing reagents (CDRs) were synthesized by incorporating amino acid amide moieties as chiral auxiliaries in trichloro-s-triazine and its 6-methoxy derivative, respectively. Another MCT reagent was synthesized by substitution of two chlorine atoms
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