N-methyl-1-(4-nitrophenyl)methanesulfonamide

Base Information

Chemical Name:N-methyl-1-(4-nitrophenyl)methanesulfonamide
CAS No.:85952-29-0
Molecular Formula:C8H10N2O4S
Molecular Weight:230.244
Hs Code.:2935009090
European Community (EC) Number:617-784-0
DSSTox Substance ID:DTXSID10351555
Nikkaji Number:J1.262.975C
Wikidata:Q72493704
Mol file:85952-29-0.mol

Synonyms:N-methyl-1-(4-nitrophenyl)methanesulfonamide;85952-29-0;N-methyl-4-nitrotoluenesulphonamide;N-METHYL-4-NITROBENZENEMETHANESULFONAMIDE;MFCD00277775;n-methyl-4-nitrobenzenemethanesulphonamide;n-methyl-(4-nitrophenyl)methanesulfonamide;Maybridge1_006642;Oprea1_403711;SCHEMBL3001018;HMS560F20;DTXSID10351555;CCG-47497;AKOS009232330;AS-7011;CS-W012959;AC-11071;N-Methyl-4-nitro-alpha-toluenesulfonamide;SY262157;{4-nitrophenyl}-N-methylmethanesulfonamide;FT-0642018;N-Methyl-4-nitro- alpha -toluenesulfonamide;EN300-680176;F30190;A841503;AR-011/42531535;SR-01000637105-1

Suppliers and Price of N-methyl-1-(4-nitrophenyl)methanesulfonamide

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

TRC
N-Methyl-1-(4-nitrophenyl)methanesulfonamide
500mg
$ 110.00

Matrix Scientific
N-Methyl-(4-nitro)-benzyl sulfonamide >97%
500mg
$ 81.00

Matrix Scientific
N-Methyl-(4-nitro)-benzyl sulfonamide >97%
5g
$ 290.00

Matrix Scientific
N-Methyl-(4-nitro)-benzyl sulfonamide >97%
1g
$ 114.00

Labseeker
4-NITRO-N-METHYLBENZENEMETHANESULFONAMIDE 95
100g
$ 3830.00

Crysdot
N-Methyl-1-(4-nitrophenyl)methanesulfonamide 98%
25g
$ 377.00

Chemenu
N-Methyl-1-(4-nitrophenyl)methanesulfonamide 95+%
25g
$ 356.00

Apolloscientific
N-Methyl-(4-nitro)-benzylsulfonamide
5g
$ 218.00

American Custom Chemicals Corporation
N-METHYL-4-NITROBENZENEMETHANESULFONAMIDE 95.00%
25G
$ 1673.60

American Custom Chemicals Corporation
N-METHYL-4-NITROBENZENEMETHANESULFONAMIDE 95.00%
1G
$ 179.66

Total 48 raw suppliers

Chemical Property of N-methyl-1-(4-nitrophenyl)methanesulfonamide

Chemical Property:

Vapor Pressure:3.53E-07mmHg at 25°C
Melting Point:151-153 °C
Refractive Index:1.579
Boiling Point:417.5 °C at 760 mmHg
PKA:10.69±0.40(Predicted)
Flash Point:206.3 °C
PSA：100.37000
Density:1.404 g/cm³
LogP:2.63890
Storage Temp.:2-8°C
XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:230.03612798
Heavy Atom Count:15
Complexity:309

Purity/Quality:

99% ^*data from raw suppliers

N-Methyl-1-(4-nitrophenyl)methanesulfonamide ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNS(=O)(=O)CC1=CC=C(C=C1)[N+](=O)[O-]
Uses N-Methyl-1-(4-nitrophenyl)methanesulfonamide is a reagent used in hydrogenation reactors in the pharmaceutical industry.

Technology Process of N-methyl-1-(4-nitrophenyl)methanesulfonamide

There total 7 articles about N-methyl-1-(4-nitrophenyl)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: 91.0%

: 85952-29-0
(4-nitro-phenyl)-methanesulfonic acid methylamide

Guidance literature:

Reference yield:

: 4025-75-6
(4-nitrophenyl)methanesulfonyl chloride

: 85952-29-0
(4-nitro-phenyl)-methanesulfonic acid methylamide

Guidance literature:: With methylamine; In dichloromethane;

Reference yield:

: 36639-50-6
Sodium 4-nitrobenzylsulphonate

: 85952-29-0
(4-nitro-phenyl)-methanesulfonic acid methylamide

Guidance literature:: Multi-step reaction with 2 steps

1: Phosphorus pentachloride

2: benzene; CHCl₃

With phosphorus pentachloride; In chloroform; benzene;
DOI:10.1002/jhet.5570230620