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4-(biphenyl-4-yloxy)aniline, also known as biphenyl-4-yloxyphenylamine, is a chemical compound that features a biphenyl group connected to an aniline group. It serves as a crucial building block in the synthesis of various organic compounds and is frequently utilized as an intermediate in the production of dyes and pigments. Due to its potential toxicity and the possibility of causing skin and eye irritation, as well as being harmful if ingested or inhaled, it is essential to handle this chemical with care and follow appropriate safety measures.

6628-69-9

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6628-69-9 Usage

Uses

Used in Chemical Synthesis:
4-(biphenyl-4-yloxy)aniline is used as a building block in the synthesis of organic compounds for various applications, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows for the creation of a wide range of derivatives with diverse properties.
Used in Dye and Pigment Production:
In the dye and pigment industry, 4-(biphenyl-4-yloxy)aniline is used as a common intermediate. Its role in the production process is crucial for creating dyes and pigments with specific color characteristics and performance attributes, which are essential for various applications such as textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 6628-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6628-69:
(6*6)+(5*6)+(4*2)+(3*8)+(2*6)+(1*9)=119
119 % 10 = 9
So 6628-69-9 is a valid CAS Registry Number.

6628-69-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-phenylphenoxy)aniline

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6628-69-9 SDS

6628-69-9Relevant academic research and scientific papers

Synthesis of a novel polyimide used as liquid crystal vertical alignment layers

Gong, Qing,Gong, Shiming,Zhang, Heng,Liu, Lulu,Wang, Yinghan

, p. 57245 - 57253 (2015)

A novel functional diamine containing a triphenylamine moiety and a biphenyl group, N,N-bis(4-aminophenyl)-4-(biphenyl)-4′-aminophenyl ether (N0), was successfully synthesized and characterized. A series of polyimides (PIs) and poly(amic acid)s (PAAs) were synthesized from cyclobutane-1,2,3,4-tetracarboxylic dianhydride (CBDA), 2,2′-bis(trifluoromethyl)-[1,1′-biphenyl]-4,4′-diamine (TFDB), 4-dodecyloxy-phenyl-4′,4″-diaminotriphenylamine (C12) and the newly synthesised diamine monomer (N0) through a conventional two-step procedure that included a ring-opening polyaddition to give polyamic acids, followed by thermal cyclodehydration. Pretilt angles of a liquid crystal (LC) cell fabricated with the PIs were measured, and the rubbing resistance of PIs containing different sidechain structures was investigated. PI1 with a rigid biphenyl side chain could induce LC parallel alignment after the rubbing process. Although PI3 containing a flexible alkyl side chain could induce LC vertical alignment before the rubbing process, it only induced LC parallel alignment after the rubbing process. However, PI2 containing both rigid biphenyl side chains and flexible alkyl side chains could induce LC vertical alignment before and after the rubbing process. A new method for improving the rubbing resistance of PIs and a generation mechanism of rubbing resistance have been proposed. In addition, all PI films showed high thermal stability and high transmittance in the wavelength range of 400-700 nm.

INHIBITORS OF NOTCH SIGNALLING PATHWAY AND USE THEREOF IN TREATMENT OF CANCERS

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Page/Page column 97-98; 100-101; 106, (2020/10/21)

The present invention relates to new inhibitors of Notch signalling pathway and its use in the treatment and/or prevention of cancers.

A focused library of protein tyrosine phosphatase inhibitors

Comeau, Anthony B.,Critton, David A.,Page, Rebecca,Seto, Christopher T.

supporting information; experimental part, p. 6768 - 6772 (2010/11/18)

Protein tyrosine phosphatases such as PTP1B and YopH are potential targets for the development of therapeutic agents against a variety of pathological conditions including diabetes, obesity, and infection by the bacterium Yersinia pestis. A focused library of bidentate α-ketoacid-based inhibitors has been screened against several tyrosine phosphatases. Compound 2a has IC 50 values of 43 and 220 nM against YopH and PTP1B, respectively, and shows a 30-fold selectivity for PTP1B over the closely related phosphatase TCPTP.

Discovery of novel and potent aryl diamines as leukotriene A4 hydrolase inhibitors

Khim, Seock-Kyu,Bauman, John,Evans, Jarred,Freeman, Beverly,King, Beverly,Kirkland, Thomas,Kochanny, Monica,Lentz, Dao,Liang, Amy,Mendoza, Lisa,Phillips, Gary,Tseng, Jih-Lie,Wei, Robert G.,Ye, Hong,Yu, Limei,Parkinson, John,Guilford, William J.

scheme or table, p. 3895 - 3898 (2009/04/07)

The synthesis and biological evaluation of a series of aryl diamines as inhibitors of LTA4-h inhibitors are described. The optimization which led to the identification of the optimal para-substitution on the diphenyl ether moiety and diamine spacer is discussed. The resulting compounds such as 3l have excellent enzyme and cellular potency as well as desirable pharmacokinetic properties.

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