n-Octylmethanesulfonamide

Base Information

Chemical Name:n-Octylmethanesulfonamide
CAS No.:16358-40-0
Molecular Formula:C9H21 N O2 S
Molecular Weight:207.337
Hs Code.:
NSC Number:116558
DSSTox Substance ID:DTXSID50936845
Nikkaji Number:J1.868.295H
Wikidata:Q82913055
Mol file:16358-40-0.mol

Synonyms:n-octylmethanesulfonamide;16358-40-0;NSC116558;N-octyl methane sulfonamide;SCHEMBL1704321;DTXSID50936845;AKOS003836794;NSC-116558

Suppliers and Price of n-Octylmethanesulfonamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of n-Octylmethanesulfonamide

Chemical Property:

Vapor Pressure:0.00185mmHg at 25°C
Boiling Point:292.3°Cat760mmHg
Flash Point:130.6°C
Density:1.001g/cm³
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:207.12930009
Heavy Atom Count:13
Complexity:194

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCNS(=O)(=O)C

Technology Process of n-Octylmethanesulfonamide

There total 2 articles about n-Octylmethanesulfonamide 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: 98.0%

: 111-86-4
n-Octylamine

: 124-63-0
methanesulfonyl chloride

: 16358-40-0
N-octylmethanesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1246/cl.2001.712

Reference yield:

: N-allyl-N-octylmethanesulfonamide

: 16358-40-0
N-octylmethanesulfonamide

Guidance literature:: With naphthalene; water; lithium; Yield given. Multistep reaction; 1.) THF, -78 deg C - 20 deg C, 12 h;
DOI:10.1016/S0040-4020(97)00920-4

Reference yield:

: 16358-40-0
N-octylmethanesulfonamide

: 124-13-0
Octanal

Guidance literature:: Multi-step reaction with 2 steps

1: N-tert-butylphenylsulfinimidoyl chloride; DBU / CH₂Cl₂ / 1 h / -78 °C

2: HCl; H₂O / diethyl ether; CH₂Cl₂ / 2 h / 50 °C

With hydrogenchloride; N-(tert-butyl)benzenesulfinimidoyl chloride; water; 1,8-diazabicyclo[5.4.0]undec-7-ene; In diethyl ether; dichloromethane;
DOI:10.1246/cl.2001.712