783325-73-5

Basic information

• Product Name: 3',5'-DiMethyl-[1,1'-biphenyl]-3-aMine
• Synonyms: 3',5'-DiMethyl-[1,1'-biphenyl]-3-aMine;3-(3,5-DiMethylphenyl)aniline
• CAS NO: 783325-73-5
• Molecular Formula: C₁₄H₁₅N
• Molecular Weight: 197.2756
• Mol File: 783325-73-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3',5'-DiMethyl-[1,1'-biphenyl]-3-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: 3',5'-DiMethyl-[1,1'-biphenyl]-3-aMine(783325-73-5)
• EPA Substance Registry System: 3',5'-DiMethyl-[1,1'-biphenyl]-3-aMine(783325-73-5)

Safety Data

• Hazardous Substances Data: 783325-73-5(Hazardous Substances Data)

Usage

General Description

3',5'-DiMethyl-[1,1'-biphenyl]-3-aMine, also known as 3,5-Dimethylaniline, is an organic compound with the chemical formula C14H15N. It is a derivative of aniline, with two methyl groups attached to the benzene ring. 3',5'-DiMethyl-[1,1'-biphenyl]-3-aMine is commonly used in the synthesis of various pharmaceuticals, dyes, and pesticides. It also has applications in the production of rubber accelerators and corrosion inhibitors. 3,5-Dimethylaniline is a colorless to pale yellow liquid with a characteristic amine odor, and it is considered to be a hazardous chemical with potential health and environmental risks. Therefore, proper safety precautions and handling procedures should be followed when working with this compound.

Upstream product

• 172975-69-8 3,5-dimethylphenyl boronic acid 
• 591-19-5 m-Bromoaniline 

Downstream Products

• 783325-75-7 N-[3-(3,5-dimethylphenyl)phenyl]anthranilic acid 
• 783325-77-9 9-bromo-3-(3',5'-dimethylphenyl)acridine 

Relevant articles and documents

Chiral 1,8-Diarylnaphthalenes, Methods of Making Them, and Their Use as Sensors

One aspect of the invention relates to 1,8-diarylnaphthalene compounds. In certain embodiments, a compound of the invention is an N-oxide of a 1,8-diarylnaphthalene. In certain embodiments, the aryl group is an optionally substituted acridyl group. In certain embodiments, a compound of the invention is a single steroisomer. In certain embodiments, a compound of the invention is a single enantiomer. Another aspect of the present invention relates to a method of detecting the presence of an analyte in a sample by monitoring the fluorescence of a compound of the invention in a sample. In certain embodiments, the analyte is a metal ion. Another aspect of the present invention relates to a method of determining the enantiomeric purity of an analyte by monitoring the fluorescence of a compound of the invention in the presence of the analyte. In certain embodiments, the analyte is a compound that is capable of hydrogen bonding.