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Terephthalbis(p-phenetidine) is a chemical compound that consists of two molecules of p-phenetidine connected to a terephthaloyl group. It is known for its unique chemical structure and properties, which make it a valuable intermediate in the production of dyes, pigments, and pharmaceuticals. Its potential applications in medical research, particularly in cancer treatment, highlight its significance in various scientific and industrial processes. However, due to potential health risks, it is crucial to handle TEREPHTHALBIS(P-PHENETIDINE) with care and follow safety guidelines.

17696-60-5

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17696-60-5 Usage

Uses

Used in Dye and Pigment Production:
Terephthalbis(p-phenetidine) is used as an intermediate in the production of dyes and pigments. Its unique chemical structure contributes to the development of various colorants used in different industries.
Used in Pharmaceutical Synthesis:
TEREPHTHALBIS(P-PHENETIDINE) is also utilized in the synthesis of pharmaceuticals, where its properties can be leveraged to create new and effective medications.
Used in Medical Research:
Terephthalbis(p-phenetidine) has potential applications in medical research, particularly in the field of cancer treatment. Its unique properties make it a valuable tool for exploring new therapeutic approaches and understanding the underlying mechanisms of cancer.
Used in Scientific and Industrial Processes:
Due to its unique chemical structure and properties, Terephthalbis(p-phenetidine) is a valuable tool in various scientific and industrial processes, where it can be used to develop new materials, products, and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 17696-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,9 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17696-60:
(7*1)+(6*7)+(5*6)+(4*9)+(3*6)+(2*6)+(1*0)=145
145 % 10 = 5
So 17696-60-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H24N2O2/c1-3-27-23-13-9-21(10-14-23)25-17-19-5-7-20(8-6-19)18-26-22-11-15-24(16-12-22)28-4-2/h5-18H,3-4H2,1-2H3/b25-17+,26-18+

17696-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-ethoxyphenyl)-1-[4-[(4-ethoxyphenyl)iminomethyl]phenyl]methanimine

1.2 Other means of identification

Product number -
Other names N,N'-(1,4-PHENYLENEDIMETHYLIDYNE)DI-P-PHENETIDINE

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:17696-60-5 SDS

17696-60-5Downstream Products

17696-60-5Relevant academic research and scientific papers

ELECTRONIC ABSORPTION SPECTRA OF AROMATIC SCHIFF BASES. PART II. TEREPHTHALDEHYDE DERIVATIVES

Muzalewski, Feliks,Gawinecki, Ryszard

, p. 565 - 572 (2007/10/02)

The effect of para substituents in the aniline moiety of terephthalidene-di(p-R-anilines) on their UV-VIS spectra has been studied.A linear relationship has been found between position of long-wavelength absorption bands of terephthalidene-dianilines with

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