Tosyl-L-lysine chloromethyl ketone
Properties
- Molecular formula
- C14H21ClN2O3S
- Molar mass
- 332.84 g/mol
- Exact mass
- 332.0961 Da
- logP
- 1.58Crippen estimate
- Polar surface area
- 89.3 Ų
- H-bond donors / acceptors
- 2 / 4
- Rotatable bonds
- 9
- Stereocentres
- Sin SMILES atom order
Identifiers
CAS number
2364-87-6SMILES
Cc1ccc(S(=O)(=O)N[C@@H](CCCCN)C(=O)CCl)cc1InChIKey
RDFCSSHDJSZMTQ-ZDUSSCGKSA-NInChI
InChI=1S/C14H21ClN2O3S/c1-11-5-7-12(8-6-11)21(19,20)17-13(14(18)10-15)4-2-3-9-16/h5-8,13,17H,2-4,9-10,16H2,1H3/t13-/m0/s1Weigh it out
Type any one amount. The others follow from the molar mass.
Names and synonyms
17 names · show all
- Benzenesulfonamide, N-[(1S)-5-amino-1-(2-chloroacetyl)pentyl]-4-methyl-
- p-Toluenesulfonamide, N-[5-amino-1-(chloroacetyl)pentyl]-, L-
- Benzenesulfonamide, N-[5-amino-1-(chloroacetyl)pentyl]-4-methyl-, (S)-
- Benzenesulfonamide, N-[(1S)-5-amino-1-(chloroacetyl)pentyl]-4-methyl-
- N-[(1S)-5-Amino-1-(2-chloroacetyl)pentyl]-4-methylbenzenesulfonamide
- 1-Chloro-3-tosylamido-7-amino-L-2-heptanone
- TLCK
- Nα-Tosyl-L-lysine chloromethyl ketone
- Nα-p-Tosyl-L-lysine chloromethyl ketone
- Tosyllysine chloromethyl ketone
- L-1-Chloro-3-tosylamido-7-amino-2-heptanone
- Tosyllysyl chloromethyl ketone
- α-N-(p-Tosyl)-L-lysyl chloromethyl ketone
- N-Tosyl-L-lysyl chloromethyl ketone
- Nα-p-Tosyl-L-lysylchloromethyl ketone
- N-Tosyl-L-lysine chloromethyl ketone
- Nα-Tosyl-L-lysyl chloromethyl ketone
Work with Tosyl-L-lysine chloromethyl ketone
Similar compounds
Nα-P-tosyl-L-lysine chloromethyl ketone hydrochloride4272-74-694 % similar
Tosyl phenylalanyl chloromethyl ketone402-71-163 % similar
N-Cyclohexyl-4-toluenesulfonamide80-30-850 % similar
Tos-arg-oh1159-15-548 % similar
α-Tosyl-L-arginine methyl ester901-47-346 % similar
N-[(4-Methylphenyl)sulfonyl]-L-glutamic acid4816-80-246 % similar
α-N-Tosyl-L-arginine methyl ester hydrochloride1784-03-844 % similar
N-[(4-Methylphenyl)sulfonyl]glycine1080-44-038 % similar
Tanimoto similarity of circular fingerprints over the whole catalogue. All similar compounds