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712728

Sigma-Aldrich

N-Tosylaziridine

98%

Synonym(s):

N-(p-Toluenesulfonyl)aziridine, N-(p-Tolylsulfonyl)aziridine

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About This Item

Empirical Formula (Hill Notation):
C9H11NO2S
CAS Number:
3634-89-7
Molecular Weight:
197.25
Beilstein:
154388
MDL number:
MFCD00188412
UNSPSC Code:
12352100
PubChem Substance ID:
329763144
NACRES:
NA.22

Quality Level

100

Assay

≥98.0% (HPLC)
98%

form

crystals

functional group

sulfonamide

storage temp.

−20°C

SMILES string

Cc1ccc(cc1)S(=O)(=O)N2CC2

InChI

1S/C9H11NO2S/c1-8-2-4-9(5-3-8)13(11,12)10-6-7-10/h2-5H,6-7H2,1H3

InChI key

VBNWSEVVMYMVLC-UHFFFAOYSA-N

Application

Reagent for beta-aminoethylation

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK0874
BCCK6147
BCCH5553
BCCG1712
BCCD2882

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Garcia-Espana, E.
Gazzetta Chimica Italiana, 115, 399-399 (1985)
Anet, F.A.L.
Journal of the American Chemical Society, 89, 357-357 (1967)
Alexander M Gilchrist et al.
Molecules (Basel, Switzerland), 25(21) (2020-11-12)
Synthetic anion transporters that facilitate chloride transport are promising candidates for channelopathy treatments. However, most anion transporters exhibit an undesired side effect of facilitating proton transport via interacting with fatty acids present in the membrane. To address the limitation, we

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