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α-[3-(4-dimesitylborylphenylazo)-4-hydroxynaphthoxy]propionic acid is a complex organic compound with the molecular formula C37H39B2N2O4S. It features a naphthoxy group, which is a naphthalene ring with a hydroxyl group attached, and an azo group connecting a 4-hydroxynaphthoxy moiety to a 4-dimesitylborylphenyl group. The propionic acid component provides an additional carboxylic acid functional group. α-[3-(4-dimesitylborylphenylazo)-4-hydroxynaphthoxy]propionic acid is characterized by its unique structure, which includes boron atoms bonded to mesityl groups, contributing to its potential applications in materials science and as a chromophore in the development of dyes or sensors. The specific arrangement of these functional groups endows the molecule with distinct chemical and physical properties, making it a subject of interest in chemical research and development.

79146-06-8

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79146-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79146-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,4 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79146-06:
(7*7)+(6*9)+(5*1)+(4*4)+(3*6)+(2*0)+(1*6)=148
148 % 10 = 8
So 79146-06-8 is a valid CAS Registry Number.

79146-06-8Downstream Products

79146-06-8Relevant academic research and scientific papers

BORON PHOTOCHEMISTRY XIV. THE DIMESITYLBORYL GROUP AS AN AUXOCHROME IN DYES: THE SYNTHESIS OF para-SUBSTITUTED DIMESITYLBORYLPHENYLAZONAPHTHOL DYES

Glogowski, M. E.,Williams, J.L.R.

, p. 1 - 8 (2007/10/02)

The dimesitylboryl group is a new auxochrome.This group was evaluated by comparison of 4--1-naphthol (III) with 4--1-naphthol (IV) and of the substituted N--1,3-benzenedisulfonamide (VIIIa) with N--1,3-benzenedisulfonamide (VIIIb).The syntheses of 5-hydroxy-8-(4-dimesitylborylphenylazo)-1-naphthyl amine (IX) and α-propionic acid (X) are reported.The visible spectra of the dimesitylboryl-containing dyes and those of the nitro analogs were similar in shape.The spectral shifts of the dimesitylboryl compounds are as great as those of the corresponding nitro analogs.However, the boryl-substituted dyes required a nondonor medium for alkalinity-induced spectral shifts.As an auxochrome the dimesitylboryl group is roughly equivalent to a nitro group.

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