371777
N-(4-Aminophenyl)-4-methylbenzenesulfonamide
99%
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About This Item
Linear Formula:
CH3C6H4SO2NHC6H4NH2
CAS Number:
Molecular Weight:
262.33
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
99%
mp
183-185 °C (lit.)
SMILES string
Cc1ccc(cc1)S(=O)(=O)Nc2ccc(N)cc2
InChI
1S/C13H14N2O2S/c1-10-2-8-13(9-3-10)18(16,17)15-12-6-4-11(14)5-7-12/h2-9,15H,14H2,1H3
InChI key
XKDFMOOUKPSLEM-UHFFFAOYSA-N
General description
N-(4-Aminophenyl)-4-methylbenzenesulfonamide is a sulfonamide derivative. It has been reported to crystallize in an asymmetric unit containing two independent molecules, having V-shaped conformations. Its crystals are orthorhombic having space group P212121.
Application
N-(4-Aminophenyl)-4-methylbenzenesulfonamide may be used in the preparation of following compounds:
- 4-methyl-N-[4-[3-(2-naphthyl)imidazo[1,2-a]pyrazine-8-yl]aminophenyl]benzenesulfonamide
- 4-methyl-N-[4-[2-(2-naphthyl)imidazo[1,2-a]pyrazine-8-yl]aminophenyl]benzenesulfonamide
- 2- and 3-substituted 8-amino imidazo[1,2-a]pyrazines
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Jeveria Rehman et al.
Acta crystallographica. Section E, Structure reports online, 67(Pt 10), o2709-o2709 (2011-11-09)
The title compound, C(13)H(14)N(2)O(2)S, crystallized with two independent mol-ecules in the asymmetric unit. They both have V-shaped conformations: the dihedral angles between their benzene rings are identical [45.86 (13)°] and their C-S-N-C torsion angles are similar [67.9 (3) and 70.2 (3)°]. In the
James R Sayer et al.
Bioorganic & medicinal chemistry, 22(22), 6459-6470 (2014-12-03)
A novel series of 8-amino imidazo[1,2-a]pyrazine derivatives has been developed as inhibitors of the VirB11 ATPase HP0525, a key component of the bacterial type IV secretion system. A flexible synthetic route to both 2- and 3-aryl substituted regioisomers has been
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