Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-

Base Information

Chemical Name:Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-
CAS No.:171414-16-7
Molecular Formula:C14H14N2O5S
Molecular Weight:322.342
Hs Code.:
DSSTox Substance ID:DTXSID50355310
Nikkaji Number:J1.570.119F
Wikidata:Q82134118
Mol file:171414-16-7.mol

Synonyms:171414-16-7;N-(4-methoxybenzyl)-2-nitrobenzenesulfonamide;Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-;N-[(4-methoxyphenyl)methyl]-2-nitrobenzenesulfonamide;CBMicro_018338;Oprea1_332344;UPCMLD00WCRH4-193;SCHEMBL6476661;DTXSID50355310;CCG-6740;STK008282;UPCMLD00WCRH4-193:002;UPCMLD00WCRH4-193:003;AKOS001287553;SB83221;BIM-0018380.P001;N-(4-methoxy-benzyl)-2-nitro-benzenesulfonamide;Z45535455;N-(4-METHOXYBENZYL)-2-NITRO-1-BENZENESULFONAMIDE

Suppliers and Price of Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-

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

American Custom Chemicals Corporation
N-(4-METHOXYBENZYL)-2-NITROBENZENESULFONAMIDE 95.00%
5MG
$ 498.01

Total 0 raw suppliers

Chemical Property of Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-

Chemical Property:

PSA：109.60000
LogP:4.07680
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:322.06234272
Heavy Atom Count:22
Complexity:463

Purity/Quality:: N-(4-METHOXYBENZYL)-2-NITROBENZENESULFONAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC=C(C=C1)CNS(=O)(=O)C2=CC=CC=C2[N+](=O)[O-]

Technology Process of Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-

There total 3 articles about Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro- 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: 97.0%

: 2393-23-9
4-methoxy-benzylamine

: 1694-92-4
2-Nitrobenzenesulfonyl chloride

: 171414-16-7
N-(4-methoxybenzyl)-2-nitro-N-(prop-2-yn-1-yl)benzenesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 23 ℃;
DOI:10.1016/0040-4039(95)01316-A

Reference yield: 95.0%

: 5455-59-4
2-Nitrobenzenesulfonamide

: 105-13-5
4-Methoxybenzyl alcohol

: 171414-16-7
N-(4-methoxybenzyl)-2-nitro-N-(prop-2-yn-1-yl)benzenesulfonamide

Guidance literature:: With 2-(diphenylphosphino)pyridine; di-tert-butyl-diazodicarboxylate; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1039/b418168a