Cas no 2104-86-1 (Benzenesulfonamide,N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl-)
![Benzenesulfonamide,N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl- structure](https://ossimg.kuujia.com/scimg/2500/2104-86-1x500.png)
2104-86-1 structure
Product Name:Benzenesulfonamide,N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl-
CAS No:2104-86-1
MF:C14H21ClN2O3S
MW:332.846141576767
CID:265555
PubChem ID:4427
Update Time:2025-04-19
Benzenesulfonamide,N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl- Chemical and Physical Properties
Names and Identifiers
-
- Benzenesulfonamide,N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl-
- TOSYLLYSINE CHLOROMETHYL KETONE
- Benzenesulfonamide, N-(5-amino-1-(chloroacetyl)pentyl)-4-methyl-
- p-Toluenesulfonamide, N-(5-amino-1-(chloroacetyl)pentyl)-, L-
- PD034268
- Chlorotosylamidoaminoheptanone
- SCHEMBL200245
- 2104-86-1
- 1-chloro-3-tosylamino-7-amino-2-heptanone
- FT-0634224
- N-(7-Amino-1-chloro-2-oxoheptan-3-yl)-4-methylbenzene-1-sulfonamide
- N-(7-amino-1-chloro-2-oxoheptan-3-yl)-4-methylbenzenesulfonamide
- CHEMBL2316089
- Tosyllysyl chloromethane
- DTXSID90859721
-
- 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
- InChI Key： RDFCSSHDJSZMTQ-UHFFFAOYSA-N
- SMILES： ClCC(C(CCCCN)NS(C1C=CC(C)=CC=1)(=O)=O)=O
Computed Properties
- Exact Mass: 332.09633
- Monoisotopic Mass: 332.096141
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 21
- Rotatable Bond Count: 9
- Complexity: 414
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 97.6
- XLogP3: 1.8
Experimental Properties
- Density: 1.242
- Boiling Point: 509.8°C at 760 mmHg
- Flash Point: 262.1°C
- Refractive Index: 1.545
- PSA: 89.26
Benzenesulfonamide,N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl- Related Literature
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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Mark D. Allendorf,Alauddin Ahmed,Tom Autrey,Jeffrey Camp,Eun Seon Cho,Maciej Haranczyk,Abhi Karkamkar,Di-Jia Liu,Katie R. Meihaus,Iffat H. Nayyar,Roman Nazarov,Donald J. Siegel,Vitalie Stavila,Jeffrey J. Urban,Srimukh Prasad Veccham,Brandon C. Wood Energy Environ. Sci., 2018,11, 2784-2812
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Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
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Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
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Eunice Y.-L. Hui,Bhimsen Rout,Yaw Sing Tan,Kok-Ping Chan,Charles W. Johannes Org. Biomol. Chem., 2018,16, 389-392
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