127502-69-6

Basic information

• Product Name: 3-(1-methylethyl)biphenyl-4-amine
• Synonyms: [1,1'-biphenyl]-4-amine, 3-(1-methylethyl)-; 3-Isopropyl-4-biphenylamine; 3-Isopropylbiphenyl-4-amine
• CAS NO: 127502-69-6
• Molecular Formula: C₁₅H₁₇N
• Molecular Weight: 211.3022
• Mol File: 127502-69-6.mol

Chemical Properties

• Boiling Point: 342.3°C at 760 mmHg
• Flash Point: 167.6°C
• Density: 1.02g/cm³
• Vapor Pressure: 7.58E-05mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: 3-(1-methylethyl)biphenyl-4-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1-methylethyl)biphenyl-4-amine(127502-69-6)
• EPA Substance Registry System: 3-(1-methylethyl)biphenyl-4-amine(127502-69-6)

Safety Data

• Hazardous Substances Data: 127502-69-6(Hazardous Substances Data)

Upstream product

• 92-93-3 1-phenyl-4-nitrobenzene 
• 1068-55-9 isopropylmagnesium chloride 
• 127502-68-5 3-isopropyl-4-nitrobiphenyl 

Relevant articles and documents

Transformation of mutagenic aromatic amines into non-mutagenic species by alkyl substituents: Part I. Alkylation ortho to the amino function

Alkyl-substituted derivatives of 2-aminonaphthalene (2-AN) 1, 2-aminofluorene (2-AF) 6 and 4-aminobiphenyl (4-ABP) 11 were synthesized and the mutagenic activity of these compounds determined in Salmonella typhimurium strains TA98 and TA100 with and without S9 mix. In the case of the ortho-substituted 4-aminobiphenyls 12-15 (3-alkyl = ethyl, iso-propyl, n-butyl, tert-butyl) the substituent with the strongest steric demand (3-tert-butyl) shows the strongest influence on the decrease of mutagenicity if compared with the parent compound. In the series of the bis-ortho-disubstituted compounds 16-18 (3,5-dimethyl-, 3,5-diethyl- and 3,5-diisopropyl-4-aminobiphenyl) generation of non-mutagenic species occurs already with the introduction of two ethyl groups. For the 4-aminobiphenyl derivatives 12-15 and 16-18, as well as for the 1-alkylated 2-aminofluorenes 7-10 and the 1-alkylated 2-aminonaphthalenes 2-5 a smaller mutagenicity was observed if compared with predicted mutagenicities as calculated by the QSAR equations of Debnath et al. (Environ. Mol. Mutagen. 19 (1992) 37). The largest differences resulted in the cases of the tert-butyl substituted compounds. Only with smaller alkyl groups like ethyl the QSAR predictions and the experimentally determined mutagenicities come close to each other. Thus, these results show that appropriate alkyl substitution reduces (eliminates) mutagenicity, secondly, it is necessary to introduce steric parameters to predict the mutagenicity of such compounds correctly.

6-phenoxymethyl-4-hydroxytetrahydropyran-2-ones and 6-thiphenoxymethyl-4-hydroxytetrahydropyran-2-ones and the corresponding dihydroxycarboxylic acid derivatives, salts and esters, and in treating hypercholesterolemia

6-Phenoxymethyl-4-hydroxytetrahydropyran-2-ones and 6-thiophenoxymethyl-4-hydroxytetrahydropyran-2-ones and the corresponding dihydroxycarboxylic acid derivatives, salts and esters, processes for the preparation of these compounds, their use as pharmaceuticals, pharmaceutical preparations and novel phenols and thiophenols Compounds of the general formula I STR1 and the corresponding open-chain dihydroxycarboxylic acids of the formula II STR2 in which X, Y and Z have the meanings given, and pharmacologically tolerated salts thereof with bases and pharmacologically tolerated esters thereof, processes for the preparation of these compounds, their use as pharmaceuticals and pharmaceutical preparations are described. Novel phenols and thiophenols of the formula III STR3 in which X, Y and Z have the meanings given, are also described.