N-tert-butyl-1-(4-chlorophenyl)methanesulfonamide

Base Information

Chemical Name:N-tert-butyl-1-(4-chlorophenyl)methanesulfonamide
CAS No.:85952-22-3
Molecular Formula:C₁₁H₁₆ClNO₂S
Molecular Weight:261.773
Hs Code.:
DSSTox Substance ID:DTXSID901206236

Synonyms:N-tert-butyl-1-(4-chlorophenyl)methanesulfonamide;DTXSID901206236;STK204516;AKOS003360564;N-(tert-butyl)(4-chlorophenyl)methanesulfonamide;SR-01000295526;SR-01000295526-1;4-Chloro-N-(1,1-dimethylethyl)benzenemethanesulfonamide;85952-22-3

Suppliers and Price of N-tert-butyl-1-(4-chlorophenyl)methanesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of N-tert-butyl-1-(4-chlorophenyl)methanesulfonamide

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:261.0590276
Heavy Atom Count:16
Complexity:308

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)NS(=O)(=O)CC1=CC=C(C=C1)Cl

Technology Process of N-tert-butyl-1-(4-chlorophenyl)methanesulfonamide

There total 1 articles about N-tert-butyl-1-(4-chlorophenyl)methanesulfonamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 6966-45-6
4-chlorobenzylsulfonyl chloride

: 75-64-9
tert-butylamine

: 85952-22-3
N-tert-Butyl-C-(4-chloro-phenyl)-methanesulfonamide

Guidance literature:: In tetrahydrofuran; 0 deg C to r.t.;
DOI:10.1021/jo00184a006

Reference yield:

: 85952-22-3
N-tert-Butyl-C-(4-chloro-phenyl)-methanesulfonamide

: C₁₁H₁₄ClLiNO₂S^(1-)*Li⁽¹⁺⁾

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 - -30 ℃;
DOI:10.1021/jo00184a006

Reference yield:

: 85952-22-3
N-tert-Butyl-C-(4-chloro-phenyl)-methanesulfonamide

: 89557-16-4,89557-17-5
1-(4-Chloro-phenyl)-2-hydroxy-2-phenyl-ethanesulfonic acid tert-butylamide

Guidance literature:: Multi-step reaction with 2 steps

1: LDA / tetrahydrofuran / -78 - -30 °C

2: Ambient temperature

With lithium diisopropyl amide; In tetrahydrofuran;
DOI:10.1021/jo00184a006