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16891-79-5,MFCD11207384
Catalog No.:AA001YB1

16891-79-5 | Benzenesulfonamide, 4-(methylamino)-

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100mg
97%
in stock  
$102.00   $71.00
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250mg
97%
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$149.00   $104.00
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1g
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$364.00   $255.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA001YB1
Chemical Name:
Benzenesulfonamide, 4-(methylamino)-
CAS Number:
16891-79-5
Molecular Formula:
C7H10N2O2S
Molecular Weight:
186.2315
MDL Number:
MFCD11207384
SMILES:
CNc1ccc(cc1)S(=O)(=O)N
Properties
Computed Properties
 
Complexity:
224  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  
XLogP3:
0.7  

Downstream Synthesis Route

[1]Hassan;Srivastava[CurrentScience,1945,vol.14,p.107]Lewis;Tager[YaleJournalofBiologyandMedicine,1940,vol.13,p.111]

[2]Oinuma;Takamura;Hasegawa;Nomoto;Naitoh;Daiku;Hamano;Kakisawa;Minami[JournalofMedicinalChemistry,1991,vol.34,#7,p.2260-2267]

[3]CurrentPatentAssignee:PFIZERINC-US2009/48282,2009,A1Locationinpatent:Page/Pagecolumn17

(E)-3,4-di-O-acetylcaffeoylchloride 
  16891-79-5   
Aceticacid2-acetoxy-5-{(E)-2-methyl-(4-sulfamoyl-phenyl)-carbamoyl-vinyl}-phenylester 

[1]Oinuma;Takamura;Hasegawa;Nomoto;Naitoh;Daiku;Hamano;Kakisawa;Minami[JournalofMedicinalChemistry,1991,vol.34,#7,p.2260-2267]

94166-64-0    16891-79-5   
5-nitro-2-(p-sulfamoylbenzylamino)pyridine 

[1]Chemicalandpharmaceuticalbulletin,1980,vol.28,p.755-760

84859-26-7    16891-79-5   
N-1-Ethyl-pyrrolidin-(2Z)-ylidene-4-methylamino-benzenesulfonamide 

[1]Ahuja;Singh;Asthana;Sardana;Anand[IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1989,vol.28,#12,p.1034-1038]

89-83-8    16891-79-5   
2-Isopropyl-5-methyl-4-(Z)-4-methylamino-phenylimino-cyclohexa-2,5-dienone 

[1]Kallmayer;Bender[Pharmazie,1997,vol.52,#3,p.210-212]

Literature

Title: Correlation analyses on binding affinity of substituted benzenesulfonamides with carbonic anhydrase using ab initio MO calculations on their complex structures (II).

Journal: Bioorganic & medicinal chemistry letters 20110101

Title: Novel use of chemical shift in NMR as molecular descriptor: a first report on modeling carbonic anhydrase inhibitory activity and related parameters.

Journal: Bioorganic & medicinal chemistry letters 20050215

Title: Carbonic anhydrase inhibitors. Inhibition of the transmembrane isozyme XII with sulfonamides-a new target for the design of antitumor and antiglaucoma drugs?

Journal: Bioorganic & medicinal chemistry letters 20050215

Title: Topological modeling of lipophilicity, diuretic activity, and carbonic inhibition activity of benzene sulfonamides: a molecular connectivity approach.

Journal: Bioorganic & medicinal chemistry letters 20041115

Title: Evidence for a membrane site of action for 14,15-EET on expression of aromatase in vascular smooth muscle.

Journal: American journal of physiology. Heart and circulatory physiology 20021101

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SDS
Tags:16891-79-5 Molecular Formula|16891-79-5 MDL|16891-79-5 SMILES|16891-79-5 Benzenesulfonamide, 4-(methylamino)-