N-Sulfanilyl-3,4-xylamide

Base Information

• Chemical Name: N-Sulfanilyl-3,4-xylamide
• CAS No.: 120-34-3
• Molecular Formula: C15H16 N2 O3 S
• Molecular Weight: 304.37
• Hs Code.: 2924299090
• European Community (EC) Number: 204-387-9
• UNII: 5QEH69594N
• DSSTox Substance ID: DTXSID30152642
• Nikkaji Number: J5.323F
• Wikidata: Q27262744
• Mol file: 120-34-3.mol

Synonyms:Xyloylsulfamine;N-Sulfanilyl-3,4-xylamide;Irgafen;120-34-3;Sulfaxylamide;Irgaphene;Sulfametoyl;Pratonal;Sulfanilyl-3,4-xylamide;Geigy 867;N-(4-aminophenyl)sulfonyl-3,4-dimethylbenzamide;G 867;3,4-Dimethyl-N-sulfanilylbenzamide;EINECS 204-387-9;BRN 2150416;Benzamide, N-((4-aminophenyl)sulfonyl)-3,4-dimethyl-;UNII-5QEH69594N;C15H16N2O3S;N-(3,4-Dimethylbenzoyl)-sulfanilamid [German];5QEH69594N;N-(4-Aminophenylsulphonyl)-3,4-dimethylbenzamide;N-((4-Aminophenyl)sulfonyl)-3,4-dimethylbenzamide;N-(3,4-Dimethylbenzoyl)-sulfanilamid;N1-(3,4-dimethylbenzoyl)sulfanilamide;Benzamide, 3,4-dimethyl-N-sulfanilyl-;n-(4-aminobenzenesulfonyl)-3,4-dimethylbenzamide;4-14-00-02665 (Beilstein Handbook Reference);Benzamide, N-[(4-aminophenyl)sulfonyl]-3,4-dimethyl-;GEIGY-867;SCHEMBL149860;DTXSID30152642;CHEBI:135290;AKOS027476303;N-SULFANILYL-3,4-XYLAMIDE [MI];LS-25622;D02438;EN300-7547665;N-(4-aminophenylsulfonyl)-3,4-dimethylbenzamide;N-[(-4-Aminophenyl)sulfonyl]-3,4-dimethylbenzamide;Q27262744;Benzamide, 3,4-dimethyl-N-sulfanilyl- (6CI,7CI,8CI);Z3244954483

Chemical Property of N-Sulfanilyl-3,4-xylamide

Chemical Property:

• Melting Point: 222-223°
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 63.19000
• Density: 1.299g/cm³
• LogP: -0.35640
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 304.08816355
• Heavy Atom Count: 21
• Complexity: 464

Purity/Quality:

98%,99%, ^*data from raw suppliers

IRGAFEN 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C=C(C=C1)C(=O)NS(=O)(=O)C2=CC=C(C=C2)N)C

Technology Process of N-Sulfanilyl-3,4-xylamide

There total 9 articles about N-Sulfanilyl-3,4-xylamide 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:

→ N-(4-aminophenylsulfonyl)-3,4-dimethylbenzamide (120-34-3)

Guidance literature:

With iron; acetic acid;

Reference yield:

3,4-dimethyl-N-sulfanilyl-benzamidine (106592-17-0) → N-(4-aminophenylsulfonyl)-3,4-dimethylbenzamide (120-34-3)

Guidance literature:

With hydrogenchloride;

Reference yield:

3,4-dimethyl-N-sulfanilyl-benzimidic acid ethyl ester → N-(4-aminophenylsulfonyl)-3,4-dimethylbenzamide (120-34-3)

Guidance literature:

With hydrogenchloride;

upstream raw materials:

3,4-dimethyl-N-sulfanilyl-benzamidine

p-acetylaminobenzenesulfonamide

3,4-dimethylbenzoyl chloride

N-methoxycarbonyl-sulfanilic acid amide

Downstream raw materials:

1-[4-(N-3,4-dimethylbenzoylsulfamoyl)-phenyl]-3-allylurea