This compound is a chiral aziridine sulfonamide derivative characterized by a benzyl substituent and a dimethylsulfamoyl group. It is primarily used as a research compound in chemical and pharmaceutical development.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
Sourcing (2S)-2-benzyl-N,N-dimethylaziridine-1-sulfonamide?
Post a free purchase request — no account needed. It reaches suppliers of this product, and replies go straight to your inbox.
Tetrabenzyl 6-[[1,3-bis(sulfanylidene)inden-2-ylidene]methyl]-16-[(Z)-(1-sulfanyl-3-sulfanylidene-1H-inden-2-ylidene)methyl]-7,10,17,20-tetrathiahexacyclo[9.9.0.02,9.04,8.012,19.014,18]icosa-1(11),2(9),4(8),5,12(19),14(18),15-heptaene-3,3,13,13-tetracarboxylate
research reagent
9-(2-Bromophenyl)-9H-carbazole
research reagent
Dehydrogenase 3alpha-hydroxy steroid
Research reagent for steroid dehydrogenase studies
5-ethyl-1-methyl-1h-tetrazole
research compound
The international HS code for (2S)-2-benzyl-N,N-dimethylaziridine-1-sulfonamide (CAS 902146-43-4) is 2933.99.
2933.99
2933 99 80
Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.
(2S)-2-benzyl-N,N-dimethylaziridine-1-sulfonamide
BLDWVIFYJWKNPQ-AMGKYWFPSA-N
CN(C)S(=O)(=O)N1C[C@@H]1CC2=CC=CC=C2
Sourcing (2S)-2-benzyl-N,N-dimethylaziridine-1-sulfonamide?
Post a free purchase request — no account needed. It reaches suppliers of this product, and replies go straight to your inbox.