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CAS RN: 35812-01-2 | Product Number: B2152

N-Bromosaccharin


Purity: >98.0%(T)
Synonyms:
  • 2-Bromo-1,2-benzisothiazol-3(2H)-one 1,1-Dioxide
Product Documents:
5G
$160.00
11   4  
25G
$487.00
12   25  

* Please contact our distributors or TCI to order our products. The above prices do not include freight cost, customs, and other charges to the destination.
* The storage conditions are subject to change without notice.


Product Number B2152
Purity / Analysis Method >98.0%(T)
Molecular Formula / Molecular Weight C__7H__4BrNO__3S = 262.08 
Physical State (20 deg.C) Solid
Storage Temperature Refrigerated (0-10°C)
Condition to Avoid Heat Sensitive
CAS RN 35812-01-2
Reaxys Registry Number 1213969
PubChem Substance ID 87565018
MDL Number

MFCD03844772

Specifications
Appearance White to Almost white powder to crystal
Purity(Iodometric Titration) min. 98.0 %
NMR confirm to structure
Properties (reference)
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P302 + P352 : IF ON SKIN: Wash with plenty of water.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
Related Laws:
Transport Information:
H.S.code* 2925.19-000
*This code is applied to the products when TCI exports from Japan and not for import in your country.
Application
N-Halosaccharin Usable for Halogenations

Experimental procedure: 1 (142 mg, 0.5 mmol) and LiClO4 (32 mg, 0.3 mmol) are dissolved in CH3CN (10 mL). The reaction mixture is stirred at room temperature for 15 min. N-Bromosaccharin (0.55 mmol) is added and stirring is continued for an additional 30 min. After removal of the solvent, the residue is dissolved in CH2Cl2 (10 mL), washed with strd. aq. NaHCO3 (3 x 10 mL), dried over Na2SO4, filtered and the solvent is evaporated in vacuo. The solid is suspended in CH3OH (4 mL) and, to remove the unwanted saccharin, undissolved pure product is filtered to obtain 2 (114 mg, 63% yield) as a white solid.

References


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