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About This Item
Linear Formula:
CH3C6H4SO2N(Cl)Na · xH2O
CAS Number:
Molecular Weight:
227.64 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352002
EC Number:
204-854-7
MDL number:
Product Name
Chloramine-T hydrate, 95%
InChI
1S/C7H7ClNO2S.Na.H2O/c1-6-2-4-7(5-3-6)12(10,11)9-8;;/h2-5H,1H3;;1H2/q-1;+1;
InChI key
BXSDMMPOQRECKB-UHFFFAOYSA-N
SMILES string
O.Cc1ccc(cc1)S(=O)(=O)N([Na])Cl
assay
95%
form
solid
reaction suitability
reagent type: oxidant
mp
167-170 °C (dec.) (lit.)
Quality Level
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Application
A review.
Capable of oxidative cyclization to produce various heterocycles.
Nitrene source for aziridinations and aminohydroxylations.
Reactant for:
- Preparation of factor Xa inhibitors as novel anticoagulants
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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Ines Sherifi et al.
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Tissue-engineered grafts may be useful in Anterior Cruciate Ligament (ACL) repair and provide a novel, alternative treatment to clinical complications of rupture, harvest site morbidity and biocompatibility associated with autografts, allografts and synthetic grafts. We successfully used supercritical carbon dioxide
J. Sci. Ind. Res., 49, 13-13 (1990)
Li, G. et al
Angewandte Chemie (International Edition in English), 35, 451-451 (1996)
Jeong, J. U. et al
Journal of the American Chemical Society, 120, 6844-6844 (1998)
Brandt, P. et al
Journal of the American Chemical Society, 122, 8013-8020 (2000)
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