13480-37-0

Basic information

• Product Name: 2-Methylbiphenyl-5-amine
• Synonyms: 2-Methylbiphenyl-5-amine;6-Methyl-[1,1'-biphenyl]-3-aMine;4-Methyl-3-phenylaniline
• CAS NO: 13480-37-0
• Molecular Formula: C₁₃H₁₃N
• Molecular Weight: 183.25
• Mol File: 13480-37-0.mol
• Article Data: 7

Chemical Properties

• Melting Point: 128-131 °C
• Boiling Point: 330.9±21.0 °C(Predicted)
• Appearance: /
• Density: 1.057±0.06 g/cm3(Predicted)
• PKA: 4.77±0.10(Predicted)
• CAS DataBase Reference: 2-Methylbiphenyl-5-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methylbiphenyl-5-amine(13480-37-0)
• EPA Substance Registry System: 2-Methylbiphenyl-5-amine(13480-37-0)

Safety Data

• Hazardous Substances Data: 13480-37-0(Hazardous Substances Data)

Upstream product

• 76472-80-5 N-(6-Methyl-biphenyl-3-yl)-acetamide 
• 7745-91-7 3-bromo-4-methylaniline 
• 98-80-6 phenylboronic acid 
• 497-19-8 sodium carbonate 
• 71-43-2 benzene 
• 99-55-8 2-methyl-5-nitroaniline 
• 40371-61-7 N-(3-bromo-4-methyl-phenyl)acetamide 
• 4870-23-9 2-p-toluidino-isoindoline-1,3-dione 
• 623-10-9 N-(4-methylphenyl)hydroxylamine 
• 539-44-6 N-4-methylphenylhydrazine 
• 13480-38-1 4-Nitro-2-phenyltoluene 

Downstream Products

• 101626-78-2 N-<6-Methyl-biphenylyl-(3)-carbamoylmethyl>-N-benzyl-aminoessigsaeure 

Relevant articles and documents

Asymmetric pyrene derivatives comprising aryl amine group and organic light-emitting diode including the same

The present invention relates to asymmetric pyrene derivatives represented by chemical formula A or chemical formula B and to an organic light-emitting device including the same, wherein substituents of Ar1, Ar2, Ar3, Ar4, Z and m are as defined in the detailed description of the present invention.

Novel thiophene amidines, compositions thereof, and methods of treating complement-mediated diseases and conditions

Disclosed is a method for treating the symptoms of an acute or chronic disorder mediated by the classical pathway of the complement cascade, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula I or a solvate, hydrate or pharmaceutically acceptable salt thereof; wherein R1, R2, R3, R4 and R7 are defined in the specification, Z is SO or SO2, and Ar is an aromatic or heteroaromatic group as defined herein.

Reaction of n-aminophthalimide derivatives with aluminum chloride in benzene

The reaction of N-aminophthalimide derivatives with AlCl3 in benzene has been investigated. From N-amino- and N-benzamidophthalimide (1a and 1b), N-amino- and N-benzamido3,3-diaryl-2,3-dihydroisoindol-1-ones (2) are obtained in high yield by initial attack of benzene on the imide carbonyl, assisted by the neighboring nitrogen atom. From N-arylaminophthalimide derivatives (4), the N-N bond is cleaved heterolytically to give an arylnitrenium ion and canonical forms involving the arene which are trapped by benzene to give aminobiaryls and N-arylanilines.