5-amino-N-(4-chlorophenyl)-2-methoxybenzenesulfonamide

Base Information

Chemical Name:5-amino-N-(4-chlorophenyl)-2-methoxybenzenesulfonamide
CAS No.:729578-90-9
Molecular Formula:C₁₃H₁₃ClN₂O₃S
Molecular Weight:312.777
Hs Code.:
DSSTox Substance ID:DTXSID701210021
Mol file:729578-90-9.mol

Synonyms:729578-90-9;5-amino-N-(4-chlorophenyl)-2-methoxybenzenesulfonamide;5-amino-N-(4-chlorophenyl)-2-methoxybenzene-1-sulfonamide;5-Amino-N-(4-chloro-phenyl)-2-methoxy-benzenesulfonamide;DTXSID701210021;AKOS000116041;SB83074;CS-0218923;EN300-02477;J-516743;Z56896200

Suppliers and Price of 5-amino-N-(4-chlorophenyl)-2-methoxybenzenesulfonamide

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
5-AMINO-N-(4-CHLORO-PHENYL)-2-METHOXY-BENZENESULFONAMIDE 95.00%
5G
$ 1114.58

American Custom Chemicals Corporation
5-AMINO-N-(4-CHLORO-PHENYL)-2-METHOXY-BENZENESULFONAMIDE 95.00%
2.5G
$ 932.60

American Custom Chemicals Corporation
5-AMINO-N-(4-CHLORO-PHENYL)-2-METHOXY-BENZENESULFONAMIDE 95.00%
1G
$ 692.46

AK Scientific
5-Amino-N-(4-chloro-phenyl)-2-methoxy-benzenesulfonamide
500mg
$ 289.00

Total 3 raw suppliers

Chemical Property of 5-amino-N-(4-chlorophenyl)-2-methoxybenzenesulfonamide

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:312.0335411
Heavy Atom Count:20
Complexity:404

Purity/Quality:

99% ^*data from raw suppliers

5-AMINO-N-(4-CHLORO-PHENYL)-2-METHOXY-BENZENESULFONAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)N)S(=O)(=O)NC2=CC=C(C=C2)Cl

Technology Process of 5-amino-N-(4-chlorophenyl)-2-methoxybenzenesulfonamide

There total 7 articles about 5-amino-N-(4-chlorophenyl)-2-methoxybenzenesulfonamide 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: 89.0%

: N-(3-(N-(4-chlorophenyl)sulfamoyl)-4-methoxyphenyl)acetamide

: 729578-90-9
C₁₃H₁₃ClN₂O₃S

Guidance literature:: With sulfuric acid; water; for 0.666667h; Reflux;
DOI:10.1007/s13738-021-02344-3

Reference yield: 87.0%

: 729578-90-9
C₁₃H₁₃ClN₂O₃S

Guidance literature:: With iron; ammonium chloride; In ethanol; water; at 20 - 90 ℃; for 2h;

Reference yield:

: 5804-73-9
5-acetamido-2-methoxybenzene-1-sulfonyl chloride

: 729578-90-9
C₁₃H₁₃ClN₂O₃S

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / neat (no solvent) / 20 °C

2: hydrogenchloride / water / 6 h / Reflux

With hydrogenchloride; sodium hydrogencarbonate; In water;
DOI:10.1007/s00706-016-1847-y